How Cannabinoid Receptors Treat Spinal Cord Injury

Source: CannabisLifeNetwork.com | Author: Travis Cesarone | Oct 19, 2022

Cannabinoid (CB) 2 receptor uptick likely occurs to protect cellular systems. CB2 receptors in the brain and gut adapt to specific cells following the loss of CB1 receptors. And a recent study assessed how cannabinoid two receptors treat spinal cord injury by recycling a critical inflammasome.

INFLAMMATORY INJURY AND ILLNESS

Earlier this year, Harvard Medical School released a pivotal study on Covid-19. The virus upticks an inflammasome, leading to a fiery cell death. I hypothesized an endocannabinoid deficiency, a major loss of 2-AG to be exact, as a crucial factor in the viral disease.

2-AG is a CB1 and CB2 receptor agonist. But cannabinoid two receptors are druggable targets that treat disease and injury caused by an inflammasome storm, including one induced by a spinal cord injury.

SPINAL CORD INJURY AND CANNABINOID RECEPTORS

According to a recent study, CB2 receptors help recycle the inflammatory protein known as NLRP3. The inflammasome remains inactive under homeostasis, a function of the endocannabinoid system. But if macrophage cells fail to clear toxins from the body, they warn the immune system, which releases NLRP3 proteins.

The process occurs in numerous diseases and leads to excessive cryopyrin. Proteins must degrade and properly recycle to avoid inflammation and pyroptosis, though. During spinal cord injury, CB2 receptor activation recycles inflammatory proteins via a unique enzymatic process — ubiquitination.

CB2 receptors, in part, boost a nutrient sensor axis (AMPK/ULK1) to recycle proteins. And NLPR3 inflammasome reduction, in turn, regulates neuron and epithelial cell polarity. CB2 receptor agonists can, therefore, regulate autophagy, prevent cell death, and attenuate neuroinflammation.

cannabinoid receptors treat spinal cord injury
“NLRP3 inflammasome structure. The NLRP3 inflammasome is a complex consisting of NLRP3, ASC, and procaspase-1. NLRP3 consists of three regions: the pyrin domain (PYD) in the amino terminus, the NACHT domain, and the leucine-rich repeat domain (LRR) in the carboxy terminus.” — Seok et al. 2021.

A DRUG OR A TERPENE?

Beta-caryophyllene and delta-9 THC agonize CB2 receptors, but THC also targets the cannabinoid one receptor. Pharmaceutical companies failed to synthesize a selective CB2 agonist over the last decade.

The value of a functional and selective CB2 receptor agonist is in the billions, despite caryophyllene’s ubiquitous presence in our food supply. Drugs or terpenes that selectively target cannabinoid two receptors can treat various conditions, including Covid-19 and spinal cord injury, by recycling inflammatory proteins.

SOURCES EXPLAINING CANNABINOID RECEPTORS ROLE

  1. Jiang F, Xia M, Zhang Y, et al. Cannabinoid receptor-2 attenuates neuroinflammation by promoting autophagy-mediated degradation of the NLRP3 inflammasome post spinal cord injury. Front Immunol. 2022;13:993168. Published 2022 Sep 26. doi:10.3389/fimmu.2022.993168
  2. Sefik E, Qu R, Junqueira C, et al. Inflammasome activation in infected macrophages drives COVID-19 pathology. Nature. 2022;606(7914):585-593. doi:10.1038/s41586-022-04802-1
  3. Seok, Jin & Kang, Han Chang & Cho, Yong-Yeon & Lee, Hye & Lee, Joo. (2021). Therapeutic regulation of the NLRP3 inflammasome in chronic inflammatory diseases. Archives of Pharmacal Research. 44. 10.1007/s12272-021-01307-9.

10 Health Benefits of CBN

Source: LinkedIn.com | Author: Arnold Benson | Oct 12, 2022

Cannabinol or (CBN) as it is called, is one of the most exciting minor cannabinoids in the cannabis plant. Much of the industry is focused on THC and CBD-based products, but research is slowly uncovering the significant therapeutic potential of minor cannabinoids like CBN on the human body.

How can CBN help medical patients? Does CBN get you high? What are the effects? CBN has many potential health benefits that can aid with everything, from insomnia to seizures and so much more. Here is what you need to know about this up-and-coming cannabinoid.

What Is this Cannabinol (CBN)?

Well CBN is a THC metabolite, for whatever that means. So in aged cannabis plants, tetrahydrocannabinol acid (THCA) degrades to cannabinolic acid (CBNA) when exposed to light and heat. Generally, cannabis plants contain trace amounts of CBN (under 1%). However, CBN concentrations can increase over time. In poor storage conditions, the plant’s THCA can degrade into CBNA, resulting in lower potency, aroma, and flavor. Cannabis processors may use various heating/extraction measures in a vacuum oven or chemical solvents to oxidize THC into CBN. This distinctive minor cannabinoid can offer many benefits for recreational, as well as medical users who make claim to being Very Effective for sleep.

When taken alone, this cannabis compound does not produce a high like THC. So let’s take a look at this in simple terms. In the human body our endocannabinoid systems (ECS), CBN has a low binding affinity with CB1 receptors BUT has a strong affinity with CB2 receptors, although it is still less than the THC. CBN appears to have similar properties as popular cannabinoids like CBD and THC.

Now the Health Benefits of CBN

  • Compared to research into other major cannabinoids like THC and CBD, CBN research is in its infancy stages. While most research into CBN is based on animal studies, researchers are beginning to uncover the potential benefits of CBN. Early research indicates that CBN may help relieve pain, insomnia, inflammation, appetite loss, and much more. CBN has many health benefits, including: Minimally psychoactive, Powerful sedative, Relieves pain, Anti-epileptic, Anti-inflammatory, Inhibits cancer cell growth, Stimulates appetite, Passes transdermal barrier ten times better than THC, Bone growth stimulation, Glaucoma treatment, Antibiotic Properties and additional scientific research is necessary to identify how this “CBN” affects the mind and body and safe ways to treat various health conditions. Simply put, CBN appears to be the cannabinoid that should not be ignored.

1. Potent Sedative –CBN is one of the most sedative cannabinoids in the cannabis plant, especially when used with THC and the myrcene terpene. Research suggests that CBN’s sedative effects can be used as a sleep aid for those who have insomnia. Not only may it help people get to sleep faster, but it may also prolong sleep time. A 5-mg dose of CBN may have the same sedative effect as 10 mg of Valium, a prescription medicine used as a sedative and for treating muscle spasms, anxiety, and alcohol withdrawal.

2. Pain Relief –Current research shows that CBN interacts with neurons involved with pain signaling and perception. These same neurons are affected by capsaicin, an active compound of chili peppers, known for its burning sensation. Capsaicin can be found in topicals and pain relievers. Essentially, CBN may be used to reduce pain.

3. Antibiotic –Studies have shown that CBN and other cannabinoids may be effective in treating MRSA, an infection caused by a type of staph bacteria. This strain of bacteria is becoming increasingly resistant to antibiotics. More research into CBN’s antimicrobial properties may help fight against antibiotic resistance.

4. Anti-Convulsant – THC and CBD products are powerful options in anti-convulsant treatment. CBN is also showing promise as a powerful anti-convulsant. A study on mice found that CBN has strong anti-convulsant properties, especially when used with other cannabinoids. If CBN continues to display anti-convulsive properties for muscle contractions, it may be a promising cannabinoid for patients with epilepsy.

5. Anti-Inflammatory – Cannabinoids can be used for inflammatory conditions such as rheumatoid arthritis and Crohn’s disease. While many cannabinoids have shown positive effects on inflammatory diseases, CBN is another alternative treatment option for those with inflammation. A study on mice found that CBN decreased allergen-induced mucus production.

6. Appetite Stimulant – Appetite loss can be caused by various psychological causes or medical conditions. While certain cannabinoids like CBD can suppress appetite, CBN may stimulate appetite. CBN may be helpful for cancer patients, for example, who may suffer from appetite loss due to cancer treatment.

7. Anti-Cancer – Early research shows that CBN can inhibit and stop cancer cell growth. In one type of lung cancer, CBN and other cannabinoids were found to actually reduce tumor size. While CBN has displayed therapeutic effects in cancer treatment, there is no definitive research showing CBN can manage the disease.

8. Glaucoma Relief – Early research suggests that high doses of CBN may help relieve intraocular pressure, a critical risk factor for glaucoma. CBN also has neuroprotective characteristics that may keep neurons in the back of the eye healthy. This is crazy but there are “Eye Drop Formulations” featuring CBN currently under development for glaucoma therapy.

9. Bone and Skin Health – CBN may have powerful protective properties to aid in bone health. CBN has been shown to activate stem cells in bones to create new bone cells. CBN may also be helpful in bone loss reduction, as a treatment for osteoporosis, and the promotion of bone healing. And in terms of skin health, CBN has been shown to reduce skin cell overgrowth. Topical CBN treatment may have promising effects in psoriasis treatment. In addition, CBN is much more permeable across the transdermal barrier than THC.

10. Neuroprotective – CBN has been shown to have neuroprotective qualities. In a study on animal models, researchers found that CBN showed positive effects when treating subjects with amyotrophic lateral sclerosis (ALS). CBN was shown to delay the onset of ALS. While more research needs to be done on humans, CBN shows promise as a therapeutic tool for neurodegenerative diseases.

FAQs About CBN

Can CBN Get You High? In small doses, CBN does not produce intoxicating effects. Is CBN Legal? While CBN is not explicitly listed under the Controlled Substances Act (CSA), CBN is still Schedule I substance derived from the Cannabis Plant Federally. The CSA defines cannabis as any part of the plant, except for stalks and nonviable seeds. CBN derived from hemp falls in a legal gray area. In some states, hemp-derived CBN products may be legal if they have under 0.3% THC. Every state has different rules and regulations on hemp-derived CBN and other THC analogs.

  • What Are High-CBN Strains? Currently, there are not many high-CBN strains compared to THC and CBD-rich varieties. Most strains have under 1% CBN. Here are a few strains that have slightly over 0.3% CBN. (Lemon Kush, Durban Poison, Blackberry, Bubble Gum, Purple Cadillac and Super Green Crack (What names lol)
  • Can You Buy CBN Online? In legal cannabis markets, CBN products can be purchased from licensed retailers. Hemp-derived CBN products are available from online retailers. Before buying CBN products, ensure they are lab-tested for purity and potency.

Final Thoughts on the Health Benefits of CBN – While THC and CBD may be the primary targets for research, CBN research is in its early stages and is slowly showcasing the health benefits of CBN. As a result, CBN is showing great promise for medical and recreational users and is being introduced into various products, including edibles and topicals.

I am so proud to be part of this movement!

How Biden’s rescheduling of marijuana could affect the US industry

Source: MJ Biz Daily | Author: Chris Roberts | Oct 14, 2022

After a half-century in which marijuana endured the strictest prohibition allowed under the law, President Joe Biden has set in motion a process that could lead to revolutionary changes for federal MJ policy.

It could mean struggling American marijuana companies can finally enjoy long-desired tax relief, or those same firms could lose cannabis entirely to big pharmaceutical companies.

Both outcomes – and many other scenarios – are all possible under the “administrative rescheduling” process the president activated last Thursday, according to legal and scientific experts.

At the same time, an act of Congress could cancel out whatever recommendations emerge from the Justice Department, the Department of Health and Human Services and the alphabet soup of other federal agencies responsible for drug policy now tasked with reviewing how Washington DC handles marijuana.

“Anyone who says they know what will happen doesn’t know what they’re talking about,” said Andrew Kline, senior counsel in the Denver office of the Perkins Coie law firm and former public policy director at the National Cannabis Industry Association.

“There are just too many unknowns at the moment.”

Under federal law, drugs fall into one of six categories, ranging from Schedule 1 to unscheduled.

And there are the five steps of the Controlled Substances Act (CSA), ranging from most to least dangerous – and restricted.

There are also many substances understood to science as “drugs” that are unscheduled.

These include popular (and potentially deadly) tonics such as alcohol and tobacco as well as the intoxicating hemp-derived delta-8 and delta-9 THC products sold online and in barely regulated smoke shops and bodegas unleashed by the 2018 Farm Bill.

The situation is more complex than some observers realize, but here’s a brief review of the rescheduling process, where marijuana could finally end up and what it would mean for the current and future U.S. cannabis industry.

Schedule 1: status quo

Background: Since 1970, cannabis has been classified under Controlled Substances Act of the Richard Nixon era as a Schedule 1 controlled substance, the category for drugs with no recognized medical application, “a high potential for abuse and the potential to create severe psychological and/or physical dependence,” according to the U.S. Drug Enforcement Administration.

Other Schedule 1 drugs include heroin, LSD and peyote.

Even in 1970, the move was controversial. In 2022, this situation “makes no sense,” the president noted last week.

Very famously, marijuana has a “lethal dose” so high it’s never been definitively established in humans, while drugs classified as Schedule 2 have a large and growing body count.

Of the 107,622 Americans killed by a drug overdose in 2021, none died from cannabis while 71,238 died from synthetic opioids such as fentanyl that a doctor could theoretically prescribe, according to the Centers for Disease Control and Prevention.

There is also growing recognition that cannabis has medicinal applications, as former U.S. Surgeon General Vivek Murthy suggested in 2015 and as a 2017 National Academies review echoed.

Though the Schedule 1 status creates an infamous Catch-22 – studies are needed to justify a rescheduling, but Schedule 1 makes cannabis harder to study, a confounding logical pretzel Congress has thus far been unable to untangle – it seems certain that marijuana will be removed from this category, experts agreed.

“Schedule 1 is a fiction,” Kline said. “There’s clear evidence of its medical utility and little evidence of the high potential for abuse.

“There’s no question it should be removed,” he added. “The question is where does it go.”

Business impact: Under Schedule 1, marijuana companies are barred from taking traditional business deductions – thanks to Section 280E of the federal tax code. That has put a major crimp on their earnings. Scientific research involving marijuana also faces heavy restrictions.

Schedule 2: pharmaceutical model

Background: Schedule 2 drugs are like Schedule 1 drugs, with one exception – clinical application with legal availability through a prescription or under supervision from a physician.

These include Adderall and Ritalin as well as cocaine, methamphetamine, fentanyl and other synthetic opioids.

Schedule 2 – the category sought by a rescheduling petition filed in 1972 by the National Organization for the Reform of Marijuana Laws (NORML) and finally rejected in 1994 – is in a way the cannabis industry’s worst nightmare: legal relief and a relaxation of prohibition but availability only via the arduous and expensive U.S. Food and Drug Administration approval process.

Business Impact: Federally legal marijuana would be “subject to tremendous testing and myriad regulatory requirements that are far beyond what states currently implement,” as The Brookings Institution scholars John Hudak and Grace Wallack wrote in 2015, when recreational cannabis sales were underway in several states in much the same fashion they are now across much of the country.

It would also quite likely still be heavily taxed, as Kline and other experts have said. Section 280E prohibits tax deductions for “trade or business” in Schedule 1 or 2 controlled substances that is “prohibited by Federal law or the law of any State in which such trade or business is conducted.”

Schedule 3-4: tax relief, but doctor’s orders

Background: Schedule 3 is where drugs with “a moderate to low potential for physical and psychological dependence,” such as Tylenol with codeine, anabolic steroids and ketamine, live.

This is the threshold “where 280E tax exemption is no longer an issue,” said Shane Pennington, a Denver-based counsel with the Vincente Sederberg law firm.

This is also the classification sought after in the thus-far symbolic bills introduced by the Congressional Cannabis Caucus that have died in committee without a hearing. That is no huge tragedy, as they currently do not stand a chance of passage in the Senate.

Yet, as Pennington observed, this also isn’t what most existing cannabis companies would want, since Schedule 3 drugs are also only generally legally available with a doctor’s authority and, thus, some level of compliance with the FDA approval process.

The same is true with drugs in Schedule 4, which have a “low potential for abuse,” such as Ambien, Ativan and Xanax.

Business impact: It’s here that the fundamental problem with using the Controlled Substances Act to regulate marijuana appears, at least in the cannabis industry’s eyes: You can’t get rid of the FDA, and the FDA process isn’t something that the current industry is built to comply with.

“People need to understand that regardless of the schedule, you’re still subject to the FDCA (Food, Drug and Cosmetic Act),” Pennington said.

“The point is that the model is not built for cannabis.”

Schedule 5: over the counter, or unscheduled?

Background: Schedule 5 drugs are still FDA-approved and regulated, but they are sold over the counter in pharmacies, supermarkets, gas stations and convenience stores like low-codeine cough syrup.

That’s exactly where most big cannabis companies would love to have their products appear – except, as Pennington pointed out, Schedule 5 products are not considered recreational or adult use.

These include cough syrup formulations.

In that analysis, no place on the Controlled Substances Act is appropriate for marijuana at all, though most observers agree that a complete removal from the CSA is something federal authorities are unlikely to recommend.

Business impact: Better from a C-suite and investors’ point of view would be total removal from the CSA – the legal status enjoyed by delta-8 and delta-9 THC products (though some states currently ban hemp-derived products sold outside their state-regulated cannabis industries).

Rescheduling, then, “would have some benefits but could unintentionally impact the 37 state medical (marijuana) programs which could effectively be dismantled were it placed into Schedule 2 or 3,” said David Holland, a New York City-based cannabis attorney.

“There would need to be a tremendous amount of federal regulation and that would only permit medical usage, not responsible adult usage.”

The upshot

What Biden might have unleashed could turn out to be “an unintended shock wave were rescheduling undertaken, rather than descheduling, which would allow the states to decide the issue of medical legalization and how it may be used in each state – medically and/or recreationally,” Holland said.

In this way, administrative rescheduling could herald tax relief and bigger margins for existing publicly traded marijuana companies.

It could also just as easily lead to an end of federal prohibition packaged with U.S. regulations so onerous that newly burdened big firms disappear and cede marijuana to something like the state-recognized small cooperatives that thrived in the early days of medical cannabis.

About the only thing known is that Biden – in making the most consequential step on federal marijuana policy of any president since Nixon – has unleashed a very long, very complex and very unpredictable force on the world that might yet wreak unintended havoc.

U.S. CBD company inks sponsorship deal with professional baseball league

Source: HempToday.com | Author: Hemp Today | Oct 13, 2022

U.S. CBD company Charlotte’s Web Holdings (CW) will pay Major League Baseball $30.5 million plus a 10% royalty on sales, and grant the professional sports organization 4% of the company’s shares in a landmark exclusive marketing deal announced this week.

Charlotte’s Web-branded products will become the “Official CBD of MLB” under the exclusive agreement, which marks the first time a professional sports league formed a sponsor partnership with a CBD company.

Increased exposure

Analysts said while the deal, which runs to 2025, won’t mean significant additional revenues for the company, it will increase the visibility of the CW brand, raise awareness of CBD products in general, and could spark similar deals in the sector. 

Charlotte’s Web Holdings, which is traded over-the-counter in Canada, recorded a net loss of ~$138 million in 2021 as revenues grew just 1.0% to reach ~$96 million. That followed a loss of ~$30 million in 2020. CW stock jumped 44% on Wednesday, following the announcement Tuesday.

CBD is not approved by the U.S. Food & Drug Administration, but MLB said in a press release that it entered the agreement after CW’s products underwent independent testing by NSF International, a consumer safety and product-testing organization, through which it met the league’s scientific standards. The league also said the products are in line with its policies on banned performance-enhancing substances.

Sports line debuts

As part of the deal, Charlotte’s Web is set to release a sports-themed line of “Daily Edge”-branded tincture, gummies, topicals and oral sprays that will feature the MLB logo. The Daily Edge tincture launched via CW’s e-commerce platform yesterday, and the brand will further debut in retail sports and health and wellness sales outlets, CW said.

“We are excited about the possibilities this partnership offers as CBD becomes a more widely adopted part of the health and wellness regimen of our players and fans,” said Noah Garden, MLB’s chief revenue officer.

Relaxed rules

MLB has stood out among other professional sports leagues in its approach to cannabis. For example, it clarified in a 2020 policy memo that players will not be punished for using cannabis away from work. However, MLB players may not enter sponsorship deals with cannabis companies or hold investments in the industry, under league policy.

In an initial promotion, CW is giving away an all-expenses paid trip to this year’s MLB World Series later this month.

Governor Newsom Signs Legislation to Strengthen California’s Cannabis Laws

Source: Gov.ca.gov | Author: Office of Governor Gavin Newsom | Sep 18, 2022

Governor signs bills to expand the legal cannabis market, address impacts from past prohibition of cannabis  

Governor calls on legislators and other policymakers to redouble efforts to tackle barriers to access

SACRAMENTO – Governor Gavin Newsom today announced that he has signed several measures to strengthen California’s cannabis laws, expand the legal cannabis market and redress the harms of cannabis prohibition.

Though the state has made significant progress since the legalization of cannabis, local opposition, rigid bureaucracy and federal prohibition continue to pose challenges to the industry and consumers. The Governor is calling on legislators and other policymakers to redouble efforts to address and eliminate these barriers.

“For too many Californians, the promise of cannabis legalization remains out of reach,” said Governor Newsom. “These measures build on the important strides our state has made toward this goal, but much work remains to build an equitable, safe and sustainable legal cannabis industry. I look forward to partnering with the Legislature and policymakers to fully realize cannabis legalization in communities across California.”

The Governor signed SB 1326 by Senator Anna Caballero (D-Merced), which creates a process for California to enter into agreements with other states to allow cannabis transactions with entities outside California. SB 1186 by Senator Scott Wiener (D-San Francisco) preempts local bans on medicinal cannabis delivery, expanding patients’ access to legal, regulated cannabis products.

The Governor also signed two bills to further unwind California’s failed history of cannabis prohibition. AB 1706 by Assemblymember Mia Bonta (D-Oakland) ensures that Californians with old cannabis-related convictions will finally have those convictions sealed. And AB 2188 by Assemblymember Bill Quirk (D-Hayward) protects Californians from employment discrimination based on their use of cannabis off-the-clock and away from the workplace.

These bills build on the Administration’s efforts to strengthen California’s cannabis legalization framework. As part of this year’s state budget, the Governor signed legislation to provide tax relief to consumers and the cannabis industry; support equity businesses; strengthen enforcement tools against illegal cannabis operators; bolster worker protections; expand access to legal retail; and protect youth, environmental and public safety programs funded by cannabis tax revenue.

To expedite policy reforms that prioritize and protect California consumers’ health and safety, the Governor has directed the California Department of Public Health to convene subject matter experts to survey current scientific research and policy mechanisms to address the growing emergence of high-potency cannabis and hemp products. The Governor has also directed the Department of Cannabis Control to further the scientific understanding of potency and its related health impacts by prioritizing the funding of research related to cannabis potency through its existing public university grants.

A full list of cannabis-related bills signed by the Governor can be found below:

  • AB 1706 by Assemblymember Mia Bonta (D-Oakland) – Cannabis crimes: resentencing.
  • AB 1646 by Assemblymember Phillip Chen (R-Yorba Linda) – Cannabis packaging: beverages.
  • AB 1885 by Assemblymember Ash Kalra (D-San Jose) – Cannabis and cannabis products: animals: veterinary medicine.
  • AB 1894 by Assemblymember Luz Rivas (D-Arleta) – Integrated cannabis vaporizer: packaging, labeling, advertisement, and marketing.
  • AB 2210 by Assemblymember Bill Quirk (D-Hayward) – Cannabis: state temporary event licenses: venues licensed by the Department of Alcoholic Beverage Control: unsold inventory.
  • AB 2188 by Assemblymember Bill Quirk (D-Hayward) – Discrimination in employment: use of cannabis.
  • AB 2568 by Assemblymember Ken Cooley (D-Rancho Cordova) – Cannabis: insurance providers.
  • AB 2925 by Assemblymember Jim Cooper (D-Elk Grove) – California Cannabis Tax Fund: spending reports.
  • SB 1186 by Senator Scott Wiener (D-San Francisco) – Medicinal Cannabis Patients’ Right of Access Act.
  • SB 1326 by Senator Anna Caballero (D-Merced) – Cannabis: interstate agreements.

Stronger Than Steel? – Hemp Rebar Could Start an Eco-Friendly Movement in Building Materials

Source: Cannabis.net | Author: Joseph Billions | Sep 3, 2022

Researchers from Rensselaer Polytechnic Institute, Troy, New York, confirm that hemp rebar could be a suitable alternative to steel in cement construction. Dan Walczyk, director of the manufacturing innovation center and professor of mechanical engineering, and Alexandros Tsamis, associate director of the Architecture Science and Ecology Center and assistant professor of architecture at Rensselaer Polytechnic, say they have produced an alternative to steel in concrete buildings and various infrastructure projects. Both scientists agree that hemp-based natural fiber-reinforced thermoplastic rebar has the potential to displace steel as the most preferred reinforcing technology in a few years. These hemp rebars are partially guaranteed to eliminate corrosion challenges, and they are more durable than steel bars.

Rebar is a crucial component in the frameworks of cement buildings. They help construct perfectly standing and durable skeletal frameworks for convention infrastructure projects. On its own, concrete lacks tensile strength, and this is the primary reason why rebars are used—to provide tensile strength.

The Manufacturing Potential of Hemp

About 150 years ago, before the onset of cannabis prohibition and the criminalization of offenders, hemp was used to produce over 75% of the goods consumed by Americans. The manufacturing of hemp-derived goods was scrapped when the government banned the cultivation and usage of the drug based on the threat of abuse. Currently, hemp is at the forefront of manufacturing discussions due to its undeniable potential to serve humans and the global ecosystem.

At the crucial point of severe environmental degradation and climate change, an environment-friendly crop like hemp could be the world’s savior. Hemp is a biodegradable harvest crop that can derive recyclables, renewables, and reusable products. For products that can’t be recycled, they are guaranteed to degrade into the environment as quickly as possible. Environmentalists who are researching the benefits of hemp claim that the mass production of the crop could go a long way towards limiting global warming effects through the reduction of carbon monoxide compounds in the air.

The industrial use of hemp plants could help produce thousands of essential items needed for day-to-day activities, including plastics, paper, clothing, linen, and drugs. It could also produce several technological tools and building items like rebar.

Hemp and the Steel Industry

Studies at Rensselaer Polytechnic and other reputable institutions point out that hemp could be a perfect replacement for steel. These scientists claim these plants are phenomenal crops meant to be mass-cultivated on industrial scales to produce dozens of products.

For example, the various car parts produced from steel or plastic can be alternatively made from hemp. And hemp is a much stronger and more durable raw material than steel and plastic. Yes, hemp is stronger than both materials and products derived from the crop that have long-lasting lifespans.

The New Study

The preliminary study confirms that hemp possesses better strength capabilities than steel and has a higher chance of substantially reducing greenhouse gas emissions.

The Rensselaer Polytechnic Institute for Energy, Built Environment, and Smart Systems (EBESS) are in charge of this new research. The institute is committed to developing a broad strategy for a durable and cost-effective hemp industry to address the constant climate change challenges in a traditionally powered ecosystem. The institute is an interdisciplinary initiative that the private school believes will close the gap between business, engineering, and design.

Walczyk and Tsamis said the research was borne out of a need for innovative and affordable hemp technologies. They also stated that hemp rebar is not the only technology being researched. These other innovations include new hemp biocomposite processing techniques and the development of decortication technology to separate hemp fibers without reducing their mechanical properties.

More Details

Concrete does not possess the internal strength required to stand on its own without support. Construction workers and engineers use steel rebars to provide tensile or inner strength. Rebars are more sturdy rods, conventionally made from steel, but not long.

The research team at the private research university published that the newly developed hemp rebars can provide the necessary framework for building and infrastructural construction. They also stressed the non-corrosive properties of proposed rebars.

Hemp is not the only material that could replace steel for construction purposes. In 1958, Roger Bacon discovered that graphite whiskers possessed ten times more tensile strength than steel and three times its stiffness. After this discovery, graphite was used to make carbon fibers. Recent findings of hemp claim hemp fibers are much stronger than these carbon fibers.

Another notable material in construction is graphene. The Science Journal discovered that graphene sheets have at least a hundred times the strength of steel. The carbon variant is an excellent conductor of electricity and can be combined with polythene products to allow conductivity. It has also been used to produce super-energy batteries and electric vehicles. The downside to this material is the cost of production. Another reason hemp is famous. The plant mimics many features of graphene, steel, and graphite whiskers. It could store as much energy as graphene and has more tensile strength than steel, and can be mass-produced at cost-effective prices.

Note that for hemp to be mass-produced for day-to-day products and industrial tools or components, there are still a few technical challenges that must be overcome. Some of this includes developing efficient processing methods and equipment that would best fit the hemp materials, manufacturing methods, and property data. Failure to overcome these hurdles would result in low-quality hemp rebar samples, among others.

Bottom Line

Hemp can be used to bring multiple high-end products to reality at far lower costs than steel and other traditional production materials. The ongoing development and research on the potential usefulness of hemp plants will shed more light on this. Rensselaer’s Seed to City Hemp Initiative will not only place the school on the hemp industry radar but also contribute to the progress of the New York engineering, design, business, and hemp industries. This proposed natural fiber-reinforced thermoplastic rebar derived from hemp plants will keep hemp structures intact for a long time.

Note that steel cannot be replaced entirely in the industry because it remains the best option for producing some substantial items and electrical tools.

Cannabis-Based Drug Kills 100% of Pancreatic Cancer Cells in New Study

Source: VeriHeal.com | Author: Chane Leigh | Sep 4, 2022

New cannabis research found that a cannabis-based drug was able to kill pancreatic cancer cells. This cannabis-based drug, or rather miraculous medication, is a botanical combination of extracts from the Cyathus striatus fungus and cannabis. This powerful combo was even able to destroy all of the cancer cells without damaging any healthy cells, unlike conventional cancer treatments.

What Is Cyathus striatus Fungus?

Cyathus striatus fungus is otherwise known as a fluted bird’s nest as a result of being a “group of gasteromycetes group of mushrooms named for their similarity in shape to small bird’s nests.” These fungi are generally considered to be inedible but not poisonous “due to their tiny size,” which is also why they are easy to miss in nature.

Cannabis-Based-Drug-Kills-100%-of-Pancreatic-Cancer-Cells-in-New-Study-2

Researchers Waill Elkhateeb and Ghoson Daba explain that this group of mushrooms has been able to “produce many novel and potent secondary metabolites that exerted different bioactivities especially as antimicrobial, antitumor, and anti-neuro inflammation activities.” The fungi found on Cyathus are saprophytes, microorganisms that live on dead organic matter. They are most commonly seen during autumn but can also be found year-round in damp and shady locations.

In their study on bird’s nest fungi, Elkhateeb and Daba explain that the “anti-inflammatory, antimicrobial and antitumor compounds isolated from these mushrooms belong to different chemical classes including steroids, terpenes, polysaccharides, fatty acids, phenolic acids and other metabolites.” However, much like cannabis, they concluded that information on these mushrooms is still unclear and that further research and investigation are needed.

Cyathus and Cannabinoids: The Cancer-Cell-Killing Duo

The treatment was developed by the biomedical company known as Cannabotech, while the study was led by Professor Faud Fares (a senior cancer researcher at the University of Haifa). The fungus was used based on the fact that it has been the subject of eight years of testing for anti-cancer properties, during which it demonstrated to have better anti-cancer results than most other fungi that were being tested.

According to PR Newswire, which reported the news from Cannabotech, the researchers made use of a cell model in order to experiment with their killer combo in order to see if it had any desirable effects on cancer cells—which it did. The cannabinoid and fungus extract duo was able to eliminate 100% of the pancreatic cancer cells in the model and it did so without damaging normal cells.

Since the Cyathus striatus fungus demonstrated better anti-cancer properties in comparison to other fungi, Fares was able to secure global and exclusive rights to use for patents he created. The professor began leading the study in an “accelerated process of developing a botanical drug as defined by the FDA.”

Cannabotech reported that the first milestone in the botanical drug development process was “defined as the adaptation of fungal growth and extraction methods to the FDA protocol for botanical drug development, which the company expects to be significantly cheaper and shorter than the development process of a standard ethical drug.” Then, the combination of the cannabinoid and fungal extract composition was examined.

The researchers were pleased to report that their cell model trial with the adapted extract was able to demonstrate five times higher anti-cancer efficacy than their original extract on top of “causing 100% mortality of pancreatic cancer cells.” They reported that they observed no damage to healthy cells in the model and that the cannabinoid extract was responsible for an 80% mortality of pancreatic cancer cells.

The team plans to complete the feasibility part of the study within 12 months (by mid-2023) and will then work with a large pharmaceutical company for its development. As part of their next milestone, the team plans to test both “the active mechanism of killing cancer cells by extracts and the combined anti-cancer efficacy of the fungus and cannabinoids together, in cells and animals.” The development of this revolutionary drug will be accompanied by Dr. Yitzhak Angel, who is a pharmacologist specializing in drug development with more than 35 years of experience.

The Stakes Are High

There are many types of fatal cancers, but pancreatic cancer is one of the most aggressive, with a very low survival rate- contributing to very high rates of mortality. So having a potential treatment for this cancer creates heaps of possibilities for other forms too. Fares stated:

“I am happy that the collaboration with Cannabotech is bearing fruit and achieving very impressive results to strengthen the research we conducted at the University of Haifa in recent years. The fact that such impressive results have been obtained in cells that mimic a subtype of pancreatic cancer that is known to be highly aggressive, reinforces the assessment that anti-cancer activity will be effective in other subtypes of pancreatic cancer as well.”

Angel, the pharmacologist consultant for Cannabotech, stated that “developing a botanical drug is a challenging process and the results we have achieved are a real indication that the extracts are effective and safe to use as an anti-cancer treatment for pancreatic cancer. We still have a way to go to substantiate that expectation, but we have good hopes to deliver real news to patients and develop a concrete solution to one of the most aggressive cancers.”

Considering the number of lives claimed by cancer and the amount of cancer-causing risks that surround us each day, research like this provides hope and comfort for those with cancer as well as those who are at high risk of developing cancer. Not only is this potential cannabis cure botanical, but it is also shaping up to be a safer and less risky treatment—which is important considering the harsh side effects associated with current cancer treatments.

Samuel Smiles, a cancer patient, stated, “Hope is like the sun, which, as we journey toward it, casts the shadow of our burden behind it”—and this research is hope.

Cannabis Users Are Just As Motivated As Everyone Else, Study Shows

Source: CannabisCulture.com | Author: Claire Wilson | Sep 4, 2022

Despite popular stereotypes, cannabis users are just as motivated as non-cannabis users.

The stereotype of the lazy stoner is a common one. It brings up images of The Dude in The Big Lebowski or a teenager next to a bong covered in snacks.

These images have plagued cannabis users but researchers at UCL, the University of Cambridge and the Institute of Psychiatry, Psychology & Neuroscience at King’s College London, have disproved this stereotype in a new study. The results show, despite popular conceptions, that regular cannabis users are just as motivated and capable of having feelings of pleasure or reward.

New Pathways to Longevity–The Endocannabinoid System and Cannabinoid-based Therapeutics

Source: CannaKeys.com | Author: Uwe Blesching | Aug 31, 2022

While our bodies can’t live forever, we can certainly work to push the boundaries of a commonly expected physical life span from seventy or seventy-five to exceed a century. And I’m not just talking about just living longer while being frail, fragile, or decrepit, but being healthy, full of life, having resilience, richness of experience, wisdom, and high level of energy. With a better understanding of the aging process and the rapidly growing scientific knowledge on how to reverse it, we now have options, our parents could have only dreamed about. And, as you will see, inducing carefully crafted changes in the endocannabinoid system (ECS), with or without the use of cannabis-based therapeutics, may turn out to play a significant role in these novel life-extension modalities. Before we dive and begin to explore what these new pathways to longevity might be it may be helpful to take a brief look at both the science of gerontology–the study of aging, and a relative newcomer to the healing arts–the cannabinoid health sciences.

Gerontology–The Science of Aging

With all our technological advances it may come as a surprise that scientists do not yet have a thorough understanding of the psycho-physiological mechanism of aging. Various theories have been proposed to explain the loss of cellular integrity that we recognize as aging (see signs and symptoms below). Such theories largely focus on ineffectual immune responses after exposure to parasites, fungi, bacteria, viruses, or other pathogens; dysfunctional autophagy (allowing  for the accumulation of older or damaged cells); mitochondrial dysfunction [i.e., the energy producing organelle that drives cellular energy levels and resulting (in)activity]; chronic or acute mental-emotional stress, physiological stressors such as the accumulation of toxins, the long-term effect of ionizing radiation, damage from exposure to free radicals (oxidative stressors); changes in hormone profiles; shortening of the end strings of DNA (i.e., telomeres, which occurs with each cell division and in the presence of stressors); and changes within the ECS1.

Graphic: Theories of Aging

With these changes we begin to experience suboptimal function at the level of the individual cell as well as the whole organism. In the case of the individual cell the mitochondria, begins to show degrees of dysfunction, resulting in a reduction in cellular energy production, an increase in mitochondrial waste (i.e., mitochondrial toxicity), loss of mitochondrial homeostasis, homeostatic dysfunctions, reduced capacity to protect against oxidative stress, and oxidative damage for instance. If not corrected this dysfunction can become a driver making us vulnerable to develop a great variety of chronic conditions such as neurological disease, immune disorders, cardio-vascular illness, and of course aging. The whole body now begins to manifest aging-related signs and symptoms.

Conversely, looking at life extension or longevity there are several methods or processes that have been posited to be able to extend life at the level of the individual cell and for the whole organism. Here in this article, we center our focus on ECS-based effects associated with the prevention and/or reversal of cognitive decline (e.g., dementia), facilitation of molecular clearance (i.e., optimization of autophagy e.g., Alzheimer’s disease), homeostatic defense activities, protection against neurodegeneration and/or neuro-inflammation (incl. neurogenesis), mitigation of oxidative stress, SIRT activation (a signaling protein with high potential for life extension), caloric restrictions (metabolism of fat cells is modulated by the ECS), mind-body approaches (stress is modulated by the ECS), and other therapeutic effects induced via the endocannabinoidome (the larger internal environment that interacts with the ECS).

The Cannabinoid Health Sciences (Endocannabinology)–

The Study of the Endocannabinoid System and Cannabinoid-based Therapeutics

The cannabinoid health sciences focus on the study of the endocannabinoid system (ECS). Fact is that all mammals—and that includes us humans—have a naturally occurring ECS.

The ECS is composed of receiving elements (cellular receptor sites i.e., CB1, CB2), their corresponding signaling components (i.e., endocannabinoids anandamide and 2-AG), and their essential building and degrading constituents (e.g., enzymes FAAH, MAGL). And while the ECS has been with us since time immemorial playing an essential role in maintaining our health and well-being, modern medicine discovered its existence and perhaps more importantly its vast therapeutic potential only in the late 1980’s. In fact, the first evidence of the existence of a mammalian receptor that binds with cannabinoids and cannabis-based constituents was discovered in the brains of rats (1988) when government researchers from the National Institutes of Mental Health (Bethesda) characterized a cannabinoid receptor that a few years later would be classified as cannabinoid receptor 1 (CB1).1 A few years later researchers from Cambridge University discovered the second later to be identified as CB2.2

Since then, the number of annual studies published in the attempt to understand and utilize the ECS in the potential treatment of more than 250 conditions has grown considerably. By 2022 an average of about 10 new studies have been published daily, signaling the excitement in the medical research community eager to make a difference in the lives of many chronic patient populations including those affected by signs and symptoms of aging.

Signs and Symptoms of Aging

Physical signs and symptoms: Wrinkles, “age spots,” greying hair, loss of muscle mass, loss of height, weight gain (associated with metabolic syndrome, insulin resistance, diabetes), loss of visual focus, loss of energy (i.e., at the level of the cell and the whole body), longer recovery times, male/female menopause, epigenetic changes, mutation, telomere shortening, loss of genetic stability and DNA repair capacities, loss of optimal organ/system functions, dysfunctional autophagy, mitochondrial dysfunction, dysfunction of the ECS, increased vulnerability to develop chronic degenerative illness associated with aging such as cancer, cardiovascular diseases, osteoporosis, and obesity for example.

Mental-emotional signs and symptoms of sub-optimal aging: may include cognitive decline or dysfunction (e.g., on a spectrum between forgetfulness–dementia), social isolation (e.g., loneliness, hopelessness), mood disorders (e.g., depression, anxiety, rapid fluctuations in mood), ruminating (esp. at night), lack of mental-emotional energy and/or focus, loss of social skills and/or functions.

The Endocannabinoid System and Aging in General

Over the past three decades the therapeutic potential of modulating the ECS for the treatment of aging and age-related human pathologies has gained momentum and significant interest, especially in the areas of cognitive decline (e.g., dementia, Alzheimer’s disease), facilitation of molecular clearance, homeostatic defense activities, neurodegeneration and/or inflammation, neurogenesis, and oxidative stress. Optimal function or dysfunction of the ECS such as modulation of the classical endocannabinoid receptor sites CB1 and CB2, or other cannabinoid sensitive receptor sites such as TRPV-1 may play a significant role in how we age.

More specifically, the capacity of the body to produce endocannabinoids, to metabolize them, as well as actual endocannabinoid receptor expression and with it optimal ECS-based signaling can change significantly as we age. You may ask why is that important? For example, a reduction in endocannabinoid receptor sites has been associated with accelerated aging. Therefore, the targeted use of cannabis-based therapeutics to support optimal ECS function and with it, optimal homeostatic responses, may mitigate several of the underlying pathologies associated with the aging process. Consider these recent discoveries highlighting several emerging insights with potential clinical applications that allow us to make informed decisions about the use of cannabis-based therapeutics to shift the typically pathological aging process to one of optimal aging:

Graphic: Young/Old Man’s Face
  • Expression of cannabinoid receptor sites and cannabinoid signaling changes as we age.1 More specifically, CB1 expression decreases by ~50% over a human life span,2 which impairs neuronal network integrity and cognitive functions.3
  • Rodents bred without CB1 receptor sites show signs of accelerated aging in the brain and skin.4
  • The ECS supports neuroprotection, is neuro-supportive, reduces oxidative stress, stabilize glial activity, mitigates glutamate excitotoxicity, aids in metabolic homeostasis, and autophagy, all of which are associated with aging.5
  • Decline of ECS-based signaling on GABAergic neurons may lead to accelerated brain aging.6
  • Deletion of CB2 leads to severe osteoporosis in the test animals indicating a significant role of CB2 in maintaining healthy bone structures in aging mammals.7
  • Enhancing CB18 and CB29 signaling enhances neurogenesis, reduces neuronal decline, and reduce the ill-effects of pathological aging upon neuroinflammation.10
  • Cannabinoids and melatonin induce therapeutic effects fundamentally related to its anti-inflammatory and antioxidative actions at the mitochondrial level.11
  • CB1 activity in the mitochondria declines with age and is associated with signs of aging such as impaired memory for example. ECS-based activity may counteract the progression of brain aging.12
  • CBD exposure to zebrafish in utero increased longevity by about 20% (in females), reduced inflammation and decreased sperm production.13
  • Only lower doses of THC increased longevity, significantly reduced weight, inflammation, and reduced several senescence markers in male zebrafish.14
  • Cannabis-based therapeutics may be effective in the treatment of nighttime agitation,15 disinhibition, irritability, and aberrant motor behavior commonly associated with dementia.16
  • A chronic low dose of Δ9-tetrahydrocannabinol (THC) restores cognitive function in old mice.17
  • The ECS may protect against aging via homeostatic defense systems such as its antioxidant effects, facilitation of clearance, anti-inflammatory effects, and initiating neuroprotection.18
  • The ECS is intricately involved in the process of central and peripheral cells.19
  • Beta-Caryophyllene, a cannabis-common terpene and FDA approved food additive binds with CB2 and protects against cognitive impairment caused by neuro-inflammation.20
  • A high cholesterol diet reduces the amount of CB1 receptor sites.21
  • A growing body of the scientific literature clearly implicates the ECS in modulating mitochondrial function22 and as such may play a significant role in several chronic pathologies including the aging process.
  • More specifically, CB1 receptors have been located at the membranes of neuronal23 and muscle24 mitochondria controlling cellular respiration and energy production with potential relevance to the aging process.
  • Similarly, FAAH the enzyme that metabolizes AEA appears to be located on the membrane of the mitochondria and as such may play a role in the aging process.25
  • CBD may reverse mitochondrial dysfunction via restoring Ca2+ homeostasis.26
  • Stress reduction techniques may halt telomere shortening or even extend them. As such cannabis, famous for its capacity to induce deep relaxation, may turn out to play a significant role in mitigating telomere-associated cellular senescence.27
  • Anandamide-induced may be a therapeutic strategy in estrogen-deficient conditions (via upregulation of heme oxygenase (HO) and nitric oxide synthase (NOS) enzymes with potential relevance to menopause.28

After this summary about the ECS and aging in general let us now look at some of the latest research findings involving sirtuins.

Graphic: Modulating Endocannabinoid Signaling to Induce Optimal Aging

SIRT1– Novel Pathways to Longevity

Sirtuins–what are they and what role do they play in life extension or anti-aging? Sirtuins are signaling proteins found in all domains of life. In humans a family of seven have been identified (i.e., produced by the genes SIRT 1-7) and to-date SIRT1 has emerged as the one most studied and with the highest potential for life extension.Some of the most important effects of SIRT1 in the context of longevity lies in the observations that:

  • SIRT1 may prevent age-related diseases and support healthy aging by protecting telomere integrity.2
  • Initiate the repair of damaged DNA (via the activation of repair proteins).3
  • Generate and maintain cellular integrity and health by inducing optimal epigenetic expressions (i.e., by turning on healthy genes and by turning off unhealthy ones).4
  • Reduces cellular energy stress during aging and age-related diseases.5
  • Optimize cellular function.6
  • Optimize cellular metabolism with relevance to age-related metabolic syndrome, obesity, diabetes, and age-related liver dysfunction (by producing a metabolic shift away from carbohydrates to the use of fat).7
  • Mitigate oxidative stress.8
  • Detoxification or clearance of old and dying cells (i.e., autophagy) thus support cellular renewal.9
  • Reduces mitochondrial damage and death and promotes energy metabolism.10
  • Similarly, to several components of the ECS, SIRT1 expression and activity too decreases with sub-optimal aging and in the presence of chronic stressors such as age-related diseases.11
  • SIRT1 activation supports optimal immune functions.12
  • Homeostatic maintenance and with it the regulation of lifespan involves SIRT1 via the hypothalamus-pituitary axis.13
Graphic: Modulating SIRT1 Signaling to Induce Optimal Aging

The Endocannabinoid System and SIRT1–Research Findings with Potential Clinical Relevance

Up to this point we explored the roles the ECS and SIRT1 play individually in mitigating the signs and symptoms of pathological aging. Now, we are ready to look at novel research results that offer additional and surprising insights. As it turns out, the reason why modulating components of the ECS with cannabis-based therapeutics (e.g., CBD) work to mitigate sub-optimal aging and as such work toward realizing longevity is at least in part due to their ability to support and harness the anti-aging effects initiated by healthy SIRT1 expressions. Consider these preclinical key findings:

  • A team of researchers from the Kunming Medical University and Hospital of People’s Liberation Army, Kaiyuan, China (2021) discovered that CBD extends the lifespan and rescues age-associated physiological declines. CBD induced autophagy and protects nerve cells from mitochondrial dysfunction via modulation of SIRT1.1
  • A multi-institutional team of Australian scientists including the Australian Centre for Cannabinoid Clinical and Research Excellence (2022) learned that upregulation in the expression of SIRT1 via the use of CBD resulted in enhanced longevity and neuroprotection.2
  • A US-based team from the National Institutes of Health, Bethesda, MD (2020) reported that antagonism at CB1 improves hepatic insulin signaling and glycemic control in obese mice via activation of SIRT1 (mTORC2/Akt pathway). To provide the reader with some practical context, the cannabis constituent THCV is a known antagonist at CB1.3
  • Another group of researchers from the Nanjing Medical University in China (2013) found additional insights implicating CB2.  More specifically, agonism at CB2 induced fatty acid oxidation via SIRT1 activation and thus may be a future target in the treatment of conditions that share an underlying pathology of lipid dysregulation.4 To provide the reader with some practical context, THC, or the cannabis-common terpene beta-caryophyllene are known agonist at CB2.

As you can see, CBD is emerging as a significant cannabinoid of interest. Future research will undoubtedly explore any potential effects (e.g., agonism vs antagonism) cannabinoids (or other cannabis-constituents) can induce via activation of CB1, CB2, other receptor sites or via the modulating of components of the endocannabinoidome (see next paragraph).

SIRT1 and the Endocannabinoidome

Curcumin

Curcumin is readily available and potent biologically active compound found in turmeric. Curcumin induces SIRT1 upregulation may be beneficial against several age-related conditions such as metabolic syndrome, obesity, and diabetes.1 It is also part of the larger endocannabinoidome i.e., the physiological environment that is responsive to changes in the ECS. For instance, while turmeric it does not bind with CB1 or CB2 it affects their actual numbers (expression) and as such may be quite able to modulate all the effects associated with these receptor sites.Emerging research findings suggest potentially significant value for patients manifesting age-related signs in the form of heart disease3 (e.g. angina, heart attack, reperfusion injuries), Alzheimer’s disease (e.g., neuroprotective, anti-inflammatory, antioxidant, improved mitochondrial functions),4 or the aging of cells that make up the lining of blood vessels and lymphatic vessels.5

Omega-3

The lipidome is a full accounting of all lipids embedded in the membranes of each individual cell. Lipids are a family of naturally occurring compounds that together build much of the internal architecture of living cells. Cellular membranes can be thought of as the skin of the cell. The skin of our trillions of individual cells is made from lipids containing a vast number of lipophilic (“fat-loving”) receptor sites such as CB1 or CB2 for example ready to interact with lipophilic compounds such as cannabinoids. Polyunsaturated fatty acids (PUFAs) are essential building blocks. Since the human body does not make its own PUFAs, we must consume them to survive and thrive. PUFAs such as omega-3 and omega-6 fatty acids are primary building blocks the body uses to make its own endocannabinoids. And here is an important insight: a healthy ECS is dependent on the ratio of omega-3 to omega-6. Excess of omega-6 and a lack of dietary omega-3 are implicated in a poorly functioning ECS.6 And, if you need another reason to motivate yourself to eat healthy fat consider that a high cholesterol diet reduces the amount of available CB1 receptor sites and with it all the potentially beneficial effects associated with them.7

Caloric Restriction

It has been posited that caloric restriction improves longevity and mitigates the development of age-related disorders (e.g., cancer)8 via several mechanism aimed at the contributing pathologies of aging including the clearance of accumulating aging and damaged cells (i.e., autophagy), improving mitochondrial energy production, and inducing antioxidant effects, for example. It is inexpensive, everyone can do it, and all is needed is the decision and the will to see it through. The good news for those of us who have a more difficult time with sticking to a diet the use of polyphenols produces similar results and as such is considered a caloric-restriction mimetic.9 Polyphenolic compounds (e.g., resveratrol, curcumin, quercetin) contained in dark grapes, turmeric, and fresh capers respectively for instance upregulate SIRT1 activity10 and as such may produce similar effects as caloric restrictions. In addition, CB1 antagonism (via a synthetic cannabinoid) has been demonstrated to create a synergy alongside caloric restriction and exercise resulting in weight-loss, improved glucose metabolism, and better cardiovascular function11 all-important markers typically used to measure signs of aging.

SIRT1 Cautions

While most of the emerging research results have explored the therapeutic potential of SIRT1 e.g., being a tumor suppressor,1 a few others have produced results that suggest that SIRT1 may act in some cases as or tumor promoter2 suggesting a more complex role (e.g., utilizing either SIRT1 agonists or antagonists) yet to be fully understood.3

In addition, overexpression of SIRT1 may induce potential adverse effects such as worsening inflammation in patients suffering from MS and autoimmune disorders such as rheumatoid arthritis.4

Furthermore, in the context of head and neck cancer SIRT1 gene silencing decreased ferroptosis (cell death induced by iron-dependent accumulation of lethal lipid peroxidation). In direct contrast, SIRT inducers such as resveratrol increased ferroptosis.5

Summary and Practical Steps to Optimize the Aging Process

While many of the longevity-related trial data is based on preclinical trials, i.e., not conducted on humans and, while much remains to be learned about how specifically cannabinoid-based therapeutics may be utilized to reach for longevity, these early findings and the potential for emerging treatment trends is already pushing the envelope of what we know about aging and the notion of life-extension itself. Here is a summary of related research findings the reader might find instructive:

Cannabidiol (CBD) is a primary cannabinoid that does not produce changes in cognition but tends to provide a gentle uplift in mood. The preclinical trials mentioned above have suggested that CBD-based modulation of various components of the ECS including that of SIRT1 may produce beneficial effects toward optimal aging.

Delta-9-tetrahydrocannabinol is the primary psychoactive compound found in cannabis. The pre-clinical trials mentioned above have suggested that small amounts of THC may be beneficial while larger amounts have produced mixed or detrimental effects. THC activates CB1 and CB2 and as such may prevent and/or mitigates cognitive decline, supports neuroprotection, anti-neuroinflammatory effects, and neurogenesis. The reader is reminded that most adverse effects associated with the use of cannabis are produced by THC in a dose-dependent fashion. In other words, the higher the mg dose of THC the higher the risk of experiencing an adverse effect. THC dosing consideration (based on usage in clinical trials): 

  • THC microdose:  0.1 mg to 0.4 mg
  • THC low dose:  0.5 mg to 5 mg
  • THC medium dose:  6 mg to 20 mg
  • THC high dose:  21 mg to 50+ mg

While already stated previously but worth repeating here, the endocannabinoidome is the larger internal environment that responds to changes in the ECS that are beyond those changes initiated by the classical endocannabinoid receptor sites (i.e., CB1 and CB2). These changes may be food-dependent, based on cannabinoid-based therapeutics, or initiated via mind-body approaches (more about that in part 2). And, since their impact can significantly support a healthy aging process, we wanted to include, at least those mentioned above, here at the very end of the article.

  • Turmeric may increase endocannabinoid receptor site expression and as such may mitigate age-dependent loss of endocannabinoid receptor sites and signaling.
  • Beta-caryophyllene activates CB2 receptor sites and may mitigate are-related neuroinflammation and associated cognitive decline.
  • Caloric restrictions, a proven life-extension method, depends, in part, on ECS-based changes in fat cell metabolism.
  • Increasing omega-3 intake may make cannabinoid more bioavailable and as such may support the beneficial effects associated with them (also consider reducing omega-6 and avoid unhealthy fats e.g., trans-fats).
  • Reducing stress and increasing activities that induce deep relaxation is significantly modulated via the ECS (more about this in part 2).

In Part 2 we will examine the latest research results focusing on where the cannabinoid health sciences overlap with research results from the field of mind-body medicine and what practical relevance and techniques can be used to mitigate pathological aging and instead to harness optimal aging and longevity.


Endnotes: Gerontology–The Science of Aging

1. Bilkei-Gorzo A. (2012). The endocannabinoid system in normal and pathological brain ageing. Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 367(1607), 3326–3341.

Endnotes: The Cannabinoid Health Sciences

1. Devane WA, Dysarz FA 3rd, Johnson MR, Melvin LS, Howlett AC (1988 Nov). Determination and characterization of a cannabinoid receptor in rat brain. Mol Pharmacol. 34(5):605-613.

2. Munro S, Thomas KL, Abu-Shaar M. (1993 Sep). Molecular characterization of a peripheral receptor for cannabinoids. Nature. 365(6441):61-5.

Endnotes: The Endocannabinoid System and Aging in General

Endnotes, graphic (Young/Old Man’s Face):

1. Kataoka K, Bilkei-Gorzo A, Nozaki C, Togo A, Nakamura K, Ohta K, Zimmer A, Asahi T. (2020 Jul) Age-dependent Alteration in Mitochondrial Dynamics and Autophagy in Hippocampal Neuron of Cannabinoid CB1 Receptor-deficient Mice. Brain Res Bull. 160:40-49.

2. Hayakawa K, Mishima K, Nozako M, Hazekawa M, Aoyama Y, Ogata A, Harada K, Fujioka M, Abe K, Egashira N, Iwasaki K, Fujiwara M. (2007 Mar) High-cholesterol feeding aggravates cerebral infarction via decreasing the CB1 receptor. Neurosci Lett. 414(2):183-7.

3. Joaquim HPG, Costa AC, Pereira CAC, Talib LL, Bilt MMV, Loch AA, Gattaz WF. Plasmatic endocannabinoids are decreased in subjects with ultra-high risk of psychosis. Eur J Neurosci. 2021 Oct 29. 

Endnotes to text:

1. Bilkei-Gorzo A. (2012). The endocannabinoid system in normal and pathological brain ageing. Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 367(1607), 3326–3341.

                  Romero J, Berrendero F, Garcia-Gil L, de la Cruz P, Ramos JA, Fernández-Ruiz JJ. (1998 Jun) Loss of cannabinoid receptor binding and messenger RNA levels and cannabinoid agonist-stimulated [35S]guanylyl-5’O-(thio)-triphosphate binding in the basal ganglia of aged rats. Neuroscience. 84(4):1075-83.

                  Berrendero F, Romero J, García-Gil L, Suarez I, De la Cruz P, Ramos JA, Fernández-Ruiz JJ. (1998 Sep 30) Changes in cannabinoid receptor binding and mRNA levels in several brain regions of aged rats. Biochim Biophys Acta. 1407(3):205-14.

                  Van Laere K, Goffin K, Casteels C, Dupont P, Mortelmans L, de Hoon J, Bormans G. Gender-dependent increases with healthy aging of the human cerebral cannabinoid-type 1 receptor binding using [(18)F]MK-9470 PET. Neuroimage. 2008 Feb 15;39(4):1533-41.

                  Wang, L., Liu, J., Harvey-White, J., Zimmer, A., & Kunos, G. (2003). Endocannabinoid signaling via cannabinoid receptor 1 is involved in ethanol preference and its age-dependent decline in mice. Proceedings of the National Academy of Sciences of the United States of America, 100(3), 1393–1398.

2. Long, L. E., Lind, J., Webster, M., & Weickert, C. S. (2012). Developmental trajectory of the endocannabinoid system in human dorsolateral prefrontal cortex. BMC neuroscience, 13, 87.

3. Kataoka K, Bilkei-Gorzo A, Nozaki C, Togo A, Nakamura K, Ohta K, Zimmer A, Asahi T. (2020 Jul) Age-dependent Alteration in Mitochondrial Dynamics and Autophagy in Hippocampal Neuron of Cannabinoid CB1 Receptor-deficient Mice. Brain Res Bull. 160:40-49.

4. Bilkei-Gorzo A, Drews E, Albayram Ö, Piyanova A, Gaffal E, Tueting T, Michel K, Mauer D, Maier W, Zimmer A. Early onset of aging-like changes is restricted to cognitive abilities and skin structure in Cnr1⁻/⁻ mice. Neurobiol Aging. 2012 Jan;33(1):200.e11-22.

5. Carrera, J., Tomberlin, J., Kurtz, J., Karakaya, E., Bostanciklioglu, M., & Albayram, O. (2021). Endocannabinoid Signaling for GABAergic-Microglia (Mis)Communication in the Brain Aging. Frontiers in neuroscience, 14, 606808.

6. Ibid.

7. Ofek, O., Karsak, M., Leclerc, N., Fogel, M., Frenkel, B., Wright, K., Tam, J., Attar-Namdar, M., Kram, V., Shohami, E., Mechoulam, R., Zimmer, A., & Bab, I. (2006). Peripheral cannabinoid receptor, CB2, regulates bone mass. Proceedings of the National Academy of Sciences of the United States of America, 103(3), 696–701.

8. Jiang, W., Zhang, Y., Xiao, L., Van Cleemput, J., Ji, S. P., Bai, G., & Zhang, X. (2005). Cannabinoids promote embryonic and adult hippocampus neurogenesis and produce anxiolytic- and antidepressant-like effects. The Journal of clinical investigation, 115(11), 3104–3116.

9. Goncalves MB, Suetterlin P, Yip P, Molina-Holgado F, Walker DJ, Oudin MJ, Zentar MP, Pollard S, Yáñez-Muñoz RJ, Williams G, Walsh FS, Pangalos MN, Doherty P. (2008 Aug) A diacylglycerol lipase-CB2 cannabinoid pathway regulates adult subventricular zone neurogenesis in an age-dependent manner. Mol Cell Neurosci. 38(4):526-36.

10. Marchalant Y, Brothers HM, Norman GJ, Karelina K, DeVries AC, Wenk GL. Cannabinoids attenuate the effects of aging upon neuroinflammation and neurogenesis. Neurobiol Dis. 2009 May;34(2):300-7.

11. García S, Martín Giménez VM, Mocayar Marón FJ, Reiter RJ, Manucha W. (2020 Aug) Melatonin and cannabinoids: mitochondrial-targeted molecules that may reduce inflammaging in neurodegenerative diseases. Histol Histopathol. 35(8):789-800.

12. Kataoka K, Bilkei-Gorzo A, Nozaki C, Togo A, Nakamura K, Ohta K, Zimmer A, Asahi T. (2020 Jul) Age-dependent Alteration in Mitochondrial Dynamics and Autophagy in Hippocampal Neuron of Cannabinoid CB1 Receptor-deficient Mice. Brain Res Bull. 160:40-49.

13. Pandelides, Z., Thornton, C., Faruque, A. S., Whitehead, A. P., Willett, K. L., & Ashpole, N. M. (2020). Developmental exposure to cannabidiol (CBD) alters longevity and health span of zebrafish (Danio rerio). GeroScience, 42(2), 785–800.

14. Pandelides, Z., Thornton, C., Lovitt, K. G., Faruque, A. S., Whitehead, A. P., Willett, K. L., & Ashpole, N. M. (2020). Developmental exposure to Δ9-tetrahydrocannabinol (THC) causes biphasic effects on longevity, inflammation, and reproduction in aged zebrafish (Danio rerio). GeroScience, 42(3), 923–936.

15. Walther S, Mahlberg R, Eichmann U, Kunz D. (2006 May) Delta-9-tetrahydrocannabinol for nighttime agitation in severe dementia. Psychopharmacology (Berl). 185(4):524-8.

16. Medical Cannabis for the Treatment of Dementia: A Review of Clinical Effectiveness and Guidelines. Ottawa: CADTH; 2019 Jul. (Canadian Agency for Drugs and Technologies in Health rapid response report: summary with critical appraisal).

17. Bilkei-Gorzo, A., Albayram, O., Draffehn, A. et al. (2017) A chronic low dose of Δ9-tetrahydrocannabinol (THC) restores cognitive function in old mice. Nat Med 23, 782–787.

18. Bilkei-Gorzo A. (2012). The endocannabinoid system in normal and pathological brain ageing. Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 367(1607), 3326–3341.

19. Paradisi A, Oddi S, Maccarrone M. (2006 Nov) The endocannabinoid system in ageing: a new target for drug development. Curr Drug Targets. 7(11):1539-52.

20. Kanojia U, Chaturbhuj SG, Sankhe R, Das M, Surubhotla R, Krishnadas N, Gourishetti K, Nayak PG, Kishore A. Beta-Caryophyllene, a CB2R Selective Agonist, Protects Against Cognitive Impairment Caused by Neuro-inflammation and Not in Dementia Due to Ageing Induced by Mitochondrial Dysfunction. CNS Neurol Disord Drug Targets. 2021;20(10):963-974.

21. Hayakawa K, Mishima K, Nozako M, Hazekawa M, Aoyama Y, Ogata A, Harada K, Fujioka M, Abe K, Egashira N, Iwasaki K, Fujiwara M. (2007 Mar) High-cholesterol feeding aggravates cerebral infarction via decreasing the CB1 receptor. Neurosci Lett. 414(2):183-7.

22. Nunn A, Guy G, Bell JD. (2012 Dec 5) Endocannabinoids in neuroendopsychology: multiphasic control of mitochondrial function. Philos Trans R Soc Lond B Biol Sci. 367(1607):3342-52.

                  Lipina C, Irving AJ, Hundal HS. (2014 Jul) Mitochondria: a possible nexus for the regulation of energy homeostasis by the endocannabinoid system? Am J Physiol Endocrinol Metab. 307(1):E1-13.

                  Fišar Z, Singh N, Hroudová J. (2014 Nov) Cannabinoid-induced changes in respiration of brain mitochondria. Toxicol Lett. 231(1):62-71.

                   Singh N, Hroudová J, Fišar Z. (2015 Aug) Cannabinoid-Induced Changes in the Activity of Electron Transport Chain Complexes of Brain Mitochondria. J Mol Neurosci. 56(4):926-931.

                  Catanzaro G, Rapino C, Oddi S, Maccarrone M. (2009 Oct 16) Anandamide increases swelling and reduces calcium sensitivity of mitochondria. Biochem Biophys Res Commun. 388(2):439-42.

                  Zhou S, Ling X, Meng P, Liang Y, Shen K, Wu Q, Zhang Y, Chen Q, Chen S, Liu Y, Zhou L. (2021 Sep) Cannabinoid receptor 2 plays a central role in renal tubular mitochondrial dysfunction and kidney ageing. J Cell Mol Med. 25(18):8957-8972.

                  Zaccagnino P, D’Oria S, Romano LL, Di Venere A, Sardanelli AM, Lorusso M. (2012 Apr) The endocannabinoid 2-arachidonoylglicerol decreases calcium induced cytochrome c release from liver mitochondria. J Bioenerg Biomembr. 44(2):273-80.

                   Lu Y, Lee DI, Roy Chowdhury S, Lu P, Kamboj A, Anderson CM, Fernyhough P, Anderson HD. (2020 Jan) Activation of Cannabinoid Receptors Attenuates Endothelin-1-Induced Mitochondrial Dysfunction in Rat Ventricular Myocytes. J Cardiovasc Pharmacol. 75(1):54-63.

                  Oláh A, Alam M, Chéret J, Kis NG, Hegyi Z, Szöllősi AG, Vidali S, Bíró T, Paus R. (. 2020 Jul) Mitochondrial energy metabolism is negatively regulated by cannabinoid receptor 1 in intact human epidermis. Exp Dermatol29(7):616-622.

23. Bénard G, Massa F, Puente N, Lourenço J, Bellocchio L, Soria-Gómez E, Matias I, Delamarre A, Metna-Laurent M, Cannich A, Hebert-Chatelain E, Mulle C, Ortega-Gutiérrez S, Martín-Fontecha M, Klugmann M, Guggenhuber S, Lutz B, Gertsch J, Chaouloff F, López-Rodríguez ML, Grandes P, Rossignol R, Marsicano G. (2012 Mar 4). Mitochondrial CB₁ receptors regulate neuronal energy metabolism. Nat Neurosci. 15(4):558-64.

                  Hebert-Chatelain E, Desprez T, Serrat R, Bellocchio L, Soria-Gomez E, Busquets-Garcia A, Pagano Zottola AC, Delamarre A, Cannich A, Vincent P, Varilh M, Robin LM, Terral G, García-Fernández MD, Colavita M, Mazier W, Drago F, Puente N, Reguero L, Elezgarai I, Dupuy JW, Cota D, Lopez-Rodriguez ML, Barreda-Gómez G, Massa F, Grandes P, Bénard G, Marsicano G. (2016 Nov 24) A cannabinoid link between mitochondria and memory. Nature. 539(7630):555-559.

                  Jimenez-Blasco D, Busquets-Garcia A, Hebert-Chatelain E, Serrat R, Vicente-Gutierrez C, Ioannidou C, Gómez-Sotres P, Lopez-Fabuel I, Resch-Beusher M, Resel E, Arnouil D, Saraswat D, Varilh M, Cannich A, Julio-Kalajzic F, Bonilla-Del Río I, Almeida A, Puente N, Achicallende S, Lopez-Rodriguez ML, Jollé C, Déglon N, Pellerin L, Josephine C, Bonvento G, Panatier A, Lutz B, Piazza PV, Guzmán M, Bellocchio L, Bouzier-Sore AK, Grandes P, Bolaños JP, Marsicano G. (2020 Jul) Glucose metabolism links astroglial mitochondria to cannabinoid effects. Nature. 583(7817):603-608.

24. Mendizabal-Zubiaga J, Melser S, Bénard G, Ramos A, Reguero L, Arrabal S, Elezgarai I, Gerrikagoitia I, Suarez J, Rodríguez De Fonseca F, Puente N, Marsicano G, Grandes P. (2016 Oct 25) Cannabinoid CB1 Receptors Are Localized in Striated Muscle Mitochondria and Regulate Mitochondrial Respiration. Front Physiol. 7:476.

25. Morozov YM, Ben-Ari Y, Freund TF. (2004 Jul) The spatial and temporal pattern of fatty acid amide hydrolase expression in rat hippocampus during postnatal development. Eur J Neurosci. 20(2):459-66.

26. Ryan D, Drysdale AJ, Lafourcade C, Pertwee RG, Platt B. (2009 Feb 18) Cannabidiol targets mitochondria to regulate intracellular Ca2+ levels. J Neurosci. 29(7):2053-63.

27. Lengacher CA, Reich RR, Kip KE, Barta M, Ramesar S, Paterson CL, Moscoso MS, Carranza I, Budhrani PH, Kim SJ, Park HY, Jacobsen PB, Schell MJ, Jim HS, Post-White J, Farias JR, Park JY. (2014 Oct) Influence of mindfulness-based stress reduction (MBSR) on telomerase activity in women with breast cancer (BC). Biol Res Nurs. 16(4):438-47.

                  Schutte NS, Malouff JM, Keng SL. (2020 Aug) Meditation and telomere length: a meta-analysis. Psychol Health. 35(8):901-915.

                  Innes KE, Selfe TK, Brundage K, Montgomery C, Wen S, Kandati S, Bowles H, Khalsa DS, Huysmans Z. (2018). Effects of Meditation and Music-Listening on Blood Biomarkers of Cellular Aging and Alzheimer’s Disease in Adults with Subjective Cognitive Decline: An Exploratory Randomized Clinical Trial. J Alzheimers Dis. 66(3):947-970.

                  Dasanayaka NN, Sirisena ND, Samaranayake N. (2021 May). The effects of meditation on length of telomeres in healthy individuals: a systematic review. Syst Rev. 10(1):151.

28. Szabó R, Börzsei D, Szabó Z, Hoffmann A, Zupkó I, Priksz D, Kupai K, Varga C, Pósa A. (2020 Nov) A Potential Involvement of Anandamide in the Modulation of HO/NOS Systems: Women, Menopause, and “Medical Cannabinoids”. Int J Mol Sci. 21(22):8801.

Graphic: Modulating Endocannabinoid Signaling to Induce Optimal Aging

1. Zheng X, Sun T, Wang X. Activation of type 2 cannabinoid receptors (CB2R) promotes fatty acid oxidation through the SIRT1/PGC-1α pathway. Biochem Biophys Res Commun. 2013 Jul 5;436(3):377-81.

2. Kang, S., Li, J., Yao, Z., & Liu, J. (2021). Cannabidiol Induces Autophagy to Protects Neural Cells from Mitochondrial Dysfunction by Upregulating SIRT1 to Inhibits NF-κB and NOTCH Pathways. Frontiers in cellular neuroscience, 15, 654340.

Wang, Z., Zheng, P., Chen, X. et al. Cannabidiol induces autophagy and improves neuronal health associated with SIRT1 mediated longevity. GeroScience (2022).

3. García S, Martín Giménez VM, Mocayar Marón FJ, Reiter RJ, Manucha W. (2020 Aug) Melatonin and cannabinoids: mitochondrial-targeted molecules that may reduce inflammation in neurodegenerative diseases. Histol Histopathol. 35(8):789-800.

                  Bénard G, Massa F, Puente N, Lourenço J, Bellocchio L, Soria-Gómez E, Matias I, Delamarre A, Metna-Laurent M, Cannich A, Hebert-Chatelain E, Mulle C, Ortega-Gutiérrez S, Martín-Fontecha M, Klugmann M, Guggenhuber S, Lutz B, Gertsch J, Chaouloff F, López-Rodríguez ML, Grandes P, Rossignol R, Marsicano G. (2012 Mar 4). Mitochondrial CB₁ receptors regulate neuronal energy metabolism. Nat Neurosci. 15(4):558-64.

                  Hebert-Chatelain E, Desprez T, Serrat R, Bellocchio L, Soria-Gomez E, Busquets-Garcia A, Pagano Zottola AC, Delamarre A, Cannich A, Vincent P, Varilh M, Robin LM, Terral G, García-Fernández MD, Colavita M, Mazier W, Drago F, Puente N, Reguero L, Elezgarai I, Dupuy JW, Cota D, Lopez-Rodriguez ML, Barreda-Gómez G, Massa F, Grandes P, Bénard G, Marsicano G. (2016 Nov 24) A cannabinoid link between mitochondria and memory. Nature. 539(7630):555-559.

                  Jimenez-Blasco D, Busquets-Garcia A, Hebert-Chatelain E, Serrat R, Vicente-Gutierrez C, Ioannidou C, Gómez-Sotres P, Lopez-Fabuel I, Resch-Beusher M, Resel E, Arnouil D, Saraswat D, Varilh M, Cannich A, Julio-Kalajzic F, Bonilla-Del Río I, Almeida A, Puente N, Achicallende S, Lopez-Rodriguez ML, Jollé C, Déglon N, Pellerin L, Josephine C, Bonvento G, Panatier A, Lutz B, Piazza PV, Guzmán M, Bellocchio L, Bouzier-Sore AK, Grandes P, Bolaños JP, Marsicano G. (2020 Jul) Glucose metabolism links astroglial mitochondria to cannabinoid effects. Nature. 583(7817):603-608.

                  Mendizabal-Zubiaga J, Melser S, Bénard G, Ramos A, Reguero L, Arrabal S, Elezgarai I, Gerrikagoitia I, Suarez J, Rodríguez De Fonseca F, Puente N, Marsicano G, Grandes P. (2016 Oct 25) Cannabinoid CB1 Receptors Are Localized in Striated Muscle Mitochondria and Regulate Mitochondrial Respiration. Front Physiol. 7:476.

4. Lengacher CA, Reich RR, Kip KE, Barta M, Ramesar S, Paterson CL, Moscoso MS, Carranza I, Budhrani PH, Kim SJ, Park HY, Jacobsen PB, Schell MJ, Jim HS, Post-White J, Farias JR, Park JY. (2014 Oct) Influence of mindfulness-based stress reduction (MBSR) on telomerase activity in women with breast cancer (BC). Biol Res Nurs. 16(4):438-47.

                  Schutte NS, Malouff JM, Keng SL. (2020 Aug) Meditation and telomere length: a meta-analysis. Psychol Health. 35(8):901-915.

                  Innes KE, Selfe TK, Brundage K, Montgomery C, Wen S, Kandati S, Bowles H, Khalsa DS, Huysmans Z. (2018). Effects of Meditation and Music-Listening on Blood Biomarkers of Cellular Aging and Alzheimer’s Disease in Adults with Subjective Cognitive Decline: An Exploratory Randomized Clinical Trial. J Alzheimers Dis. 66(3):947-970.

                  Dasanayaka NN, Sirisena ND, Samaranayake N. (2021 May). The effects of meditation on length of telomeres in healthy individuals: a systematic review. Syst Rev. 10(1):151.

5. Szabó R, Börzsei D, Szabó Z, Hoffmann A, Zupkó I, Priksz D, Kupai K, Varga C, Pósa A. (2020 Nov 20) A Potential Involvement of Anandamide in the Modulation of HO/NOS Systems: Women, Menopause, and “Medical Cannabinoids”. Int J Mol Sci. 21(22):8801.

6. Pandelides, Z., Thornton, C., Faruque, A. S., Whitehead, A. P., Willett, K. L., & Ashpole, N. M. (2020). Developmental exposure to cannabidiol (CBD) alters longevity and health span of zebrafish (Danio rerio). GeroScience, 42(2), 785–800.

                  Kang, S., Li, J., Yao, Z., & Liu, J. (2021). Cannabidiol Induces Autophagy to Protects Neural Cells from Mitochondrial Dysfunction by Upregulating SIRT1 to Inhibits NF-κB and NOTCH Pathways. Frontiers in cellular neuroscience, 15, 654340.

                  Wang, Z., Zheng, P., Chen, X. et al. Cannabidiol induces autophagy and improves neuronal health associated with SIRT1 mediated longevity. GeroScience (2022).

7. See 1-6 above.

Endnotes: SIRT1– Novel Pathways to Longevity

1. Grabowska, W., Sikora, E., & Bielak-Zmijewska, A. (2017). Sirtuins, a promising target in slowing down the ageing process. Biogerontology, 18(4), 447–476.

2. Osum M, Serakinci N. Impact of circadian disruption on health; SIRT1 and Telomeres. DNA Repair (Amst). 2020 Dec;96:102993.

3. Oberdoerffer, P., Michan, S., McVay, M., Mostoslavsky, R., Vann, J., Park, S. K., Hartlerode, A., Stegmuller, J., Hafner, A., Loerch, P., Wright, S. M., Mills, K. D., Bonni, A., Yankner, B. A., Scully, R., Prolla, T. A., Alt, F. W., & Sinclair, D. A. (2008). SIRT1 redistribution on chromatin promotes genomic stability but alters gene expression during aging. Cell, 135(5), 907–918.

                  Ming, M., Shea, C. R., Guo, X., Li, X., Soltani, K., Han, W., & He, Y. Y. (2010). Regulation of global genome nucleotide excision repair by SIRT1 through xeroderma pigmentosum C. Proceedings of the National Academy of Sciences of the United States of America, 107(52), 22623–22628.

                  Wang, R. H., Sengupta, K., Li, C., Kim, H. S., Cao, L., Xiao, C., Kim, S., Xu, X., Zheng, Y., Chilton, B., Jia, R., Zheng, Z. M., Appella, E., Wang, X. W., Ried, T., & Deng, C. X. (2008). Impaired DNA damage response, genome instability, and tumorigenesis in SIRT1 mutant mice. Cancer cell, 14(4), 312–323.

                  Chung, S., Yao, H., Caito, S., Hwang, J. W., Arunachalam, G., & Rahman, I. (2010). Regulation of SIRT1 in cellular functions: role of polyphenols. Archives of biochemistry and biophysics, 501(1), 79–90.

4. Zhou CH, Zhang MX, Zhou SS, Li H, Gao J, Du L, Yin XX. SIRT1 attenuates neuropathic pain by epigenetic regulation of mGluR1/5 expressions in type 2 diabetic rats. Pain. 2017 Jan;158(1):130-139.

5. Fang, Y., Wang, X., Yang, D., Lu, Y., Wei, G., Yu, W., Liu, X., Zheng, Q., Ying, J., & Hua, F. (2021). Relieving Cellular Energy Stress in Aging, Neurodegenerative, and Metabolic Diseases, SIRT1 as a Therapeutic and Promising Node. Frontiers in aging neuroscience, 13, 738686.

6. Chung, S., Yao, H., Caito, S., Hwang, J. W., Arunachalam, G., & Rahman, I. (2010). Regulation of SIRT1 in cellular functions: role of polyphenols. Archives of biochemistry and biophysics, 501(1), 79–90.

7. Sasaki T. (2015). Age-Associated Weight Gain, Leptin, and SIRT1: A Possible Role for Hypothalamic SIRT1 in the Prevention of Weight Gain and Aging through Modulation of Leptin Sensitivity. Frontiers in endocrinology, 6, 109.

Milne, J. C., Lambert, P. D., Schenk, S., Carney, D. P., Smith, J. J., Gagne, D. J., Jin, L., Boss, O., Perni, R. B., Vu, C. B., Bemis, J. E., Xie, R., Disch, J. S., Ng, P. Y., Nunes, J. J., Lynch, A. V., Yang, H., Galonek, H., Israelian, K., Choy, W., … Westphal, C. H. (2007). Small molecule activators of SIRT1 as therapeutics for the treatment of type 2 diabetes. Nature, 450(7170), 712–716.

Jin, J., Iakova, P., Jiang, Y., Medrano, E. E., & Timchenko, N. A. (2011). The reduction of SIRT1 in livers of old mice leads to impaired body homeostasis and to inhibition of liver proliferation. Hepatology (Baltimore, Md.), 54(3), 989–998.

Li Z, Zhang Z, Ke L, Sun Y, Li W, Feng X, Zhu W, Chen S. (2020 Mar) Resveratrol promotes white adipocytes browning and improves metabolic disorders in Sirt1-dependent manner in mice. FASEB J. 34(3):4527-4539.

Timmers, S., Konings, E., Bilet, L., Houtkooper, R. H., van de Weijer, T., Goossens, G. H., Hoeks, J., van der Krieken, S., Ryu, D., Kersten, S., Moonen-Kornips, E., Hesselink, M., Kunz, I., Schrauwen-Hinderling, V. B., Blaak, E., Auwerx, J., & Schrauwen, P. (2011). Calorie restriction-like effects of 30 days of resveratrol supplementation on energy metabolism and metabolic profile in obese humans. Cell metabolism, 14(5), 612–622.

8. Guarente L. Sirtuins in aging and disease. Cold Spring Harb Symp Quant Biol. 2007;72:483-8.

9. Lee, I. H., Cao, L., Mostoslavsky, R., Lombard, D. B., Liu, J., Bruns, N. E., Tsokos, M., Alt, F. W., & Finkel, T. (2008). A role for the NAD-dependent deacetylase Sirt1 in the regulation of autophagy. Proceedings of the National Academy of Sciences of the United States of America, 105(9), 3374–3379.

10. Huang Q, Su H, Qi B, Wang Y, Yan K, Wang X, Li X, Zhao D. A SIRT1 Activator, Ginsenoside Rc, Promotes Energy Metabolism in Cardiomyocytes and Neurons. J Am Chem Soc. 2021 Jan 27;143(3):1416-1427.

11. Fang, Y., Wang, X., Yang, D., Lu, Y., Wei, G., Yu, W., Liu, X., Zheng, Q., Ying, J., & Hua, F. (2021). Relieving Cellular Energy Stress in Aging, Neurodegenerative, and Metabolic Diseases, SIRT1 as a Therapeutic and Promising Node. Frontiers in aging neuroscience, 13, 738686.

12. Hamaidi, I., Kim, S. Sirtuins are crucial regulators of T cell metabolism and functions. (2022) Exp Mol Med 54, 207–215.

13. Yamamoto M, Takahashi Y. (2018 Oct) The Essential Role of SIRT1 in Hypothalamic-Pituitary Axis. Front Endocrinol (Lausanne). 9:605.

Graphic: Modulating SIRT1 Signaling to Induce Optimal Aging

1. Hamaidi, I., Kim, S. Sirtuins are crucial regulators of T cell metabolism and functions. Exp Mol Med 54, 207–215 (2022).

2. Lee, I. H., Cao, L., Mostoslavsky, R., Lombard, D. B., Liu, J., Bruns, N. E., Tsokos, M., Alt, F. W., & Finkel, T. (2008).  A role for the NAD-dependent deacetylase Sirt1 in the regulation of autophagy. Proceedings of the National Academy of Sciences of the United States of America, 105(9), 3374–3379.

3. Huang Q, Su H, Qi B, Wang Y, Yan K, Wang X, Li X, Zhao D. A SIRT1 Activator, Ginsenoside Rc, Promotes Energy Metabolism in Cardiomyocytes and Neurons. J Am Chem Soc. 2021 Jan 27;143(3):1416-1427.

4. Osum M, Serakinci N. Impact of circadian disruption on health; SIRT1 and Telomeres. DNA Repair (Amst). 2020 Dec;96:102993.

5. Yamamoto M, Takahashi Y. (2018 Oct) The Essential Role of SIRT1 in Hypothalamic-Pituitary Axis. Front Endocrinol (Lausanne). 9:605.

6. Zhou CH, Zhang MX, Zhou SS, Li H, Gao J, Du L, Yin XX. SIRT1 attenuates neuropathic pain by epigenetic regulation of mGluR1/5 expressions in type 2 diabetic rats. Pain. 2017 Jan;158(1):130-139.

7. Pandelides, Z., Thornton, C., Faruque, A. S., Whitehead, A. P., Willett, K. L., & Ashpole, N. M. (2020). Developmental exposure to cannabidiol (CBD) alters longevity and health span of zebrafish (Danio rerio). GeroScience, 42(2), 785–800.

                  Kang, S., Li, J., Yao, Z., & Liu, J. (2021). Cannabidiol Induces Autophagy to Protects Neural Cells from Mitochondrial Dysfunction by Upregulating SIRT1 to Inhibits NF-κB and NOTCH Pathways. Frontiers in cellular neuroscience, 15, 654340.

                  Wang, Z., Zheng, P., Chen, X. et al. Cannabidiol induces autophagy and improves neuronal health associated with SIRT1 mediated longevity. GeroScience (2022).

 Bilkei-Gorzo, A., Albayram, O., Draffehn, A. et al. (2017) A chronic low dose of Δ9-tetrahydrocannabinol (THC) restores cognitive function in old mice. Nat Med 23, 782–787.

                  Pandelides, Z., Thornton, C., Lovitt, K. G., Faruque, A. S., Whitehead, A. P., Willett, K. L., & Ashpole, N. M. (2020). Developmental exposure to Δ9-tetrahydrocannabinol (THC) causes biphasic effects on longevity, inflammation, and reproduction in aged zebrafish (Danio rerio). GeroScience, 42(3), 923–936.

 Liu, J., Godlewski, G., Jourdan, T., Liu, Z., Cinar, R., Xiong, K., & Kunos, G. (2019). Cannabinoid-1 Receptor Antagonism Improves Glycemic Control and Increases Energy Expenditure Through Sirtuin-1/Mechanistic Target of Rapamycin Complex 2 and 5’Adenosine Monophosphate-Activated Protein Kinase Signaling. Hepatology (Baltimore, Md.), 69(4), 1535–1548.

 Zheng X, Sun T, Wang X. Activation of type 2 cannabinoid receptors (CB2R) promotes fatty acid oxidation through the SIRT1/PGC-1α pathway. Biochem Biophys Res Commun. 2013 Jul 5;436(3):377-81.

 Hassanzadeh P, Hassanzadeh A (2012) The CB1 receptor-mediated endocannabinoid signaling and NGF: the novel targets of curcumin. Neurochemical Research 37: 1112–1120.

                  Zhang Z, Guo Y, Zhang S, et al. Curcumin modulates cannabinoid receptors in liver fibrosis in vivo and inhibits extracellular matrix expression in hepatic stellate cells by suppressing cannabinoid receptor type-1 in vitro. Eur J Pharmacol. 2013;721(1-3):133–140.

Endnotes: The Endocannabinoid System and SIRT1

1. Kang, S., Li, J., Yao, Z., & Liu, J. (2021). Cannabidiol Induces Autophagy to Protects Neural Cells from Mitochondrial Dysfunction by Upregulating SIRT1 to Inhibits NF-κB and NOTCH Pathways. Frontiers in cellular neuroscience, 15, 654340.

2. Wang, Z., Zheng, P., Chen, X. et al. Cannabidiol induces autophagy and improves neuronal health associated with SIRT1 mediated longevity. GeroScience (2022).

3. Liu, J., Godlewski, G., Jourdan, T., Liu, Z., Cinar, R., Xiong, K., & Kunos, G. (2019). Cannabinoid-1 Receptor Antagonism Improves Glycemic Control and Increases Energy Expenditure Through Sirtuin-1/Mechanistic Target of Rapamycin Complex 2 and 5’Adenosine Monophosphate-Activated Protein Kinase Signaling. Hepatology (Baltimore, Md.), 69(4), 1535–1548.

4. Zheng X, Sun T, Wang X. Activation of type 2 cannabinoid receptors (CB2R) promotes fatty acid oxidation through the SIRT1/PGC-1α pathway. Biochem Biophys Res Commun. 2013 Jul 5;436(3):377-81.

Endnotes: SIRT1 and the Endocannabinoidome

1. Zendedel E, Butler AE, Atkin SL, Sahebkar A. Impact of curcumin on sirtuins: A review. J Cell Biochem. 2018 Dec;119(12):10291-10300.

2. Hassanzadeh P, Hassanzadeh A (2012) The CB1 receptor-mediated endocannabinoid signaling and NGF: the novel targets of curcumin. Neurochemical Research 37: 1112–1120.

Zhang Z, Guo Y, Zhang S, et al. Curcumin modulates cannabinoid receptors in liver fibrosis in vivo and inhibits extracellular matrix expression in hepatic stellate cells by suppressing cannabinoid receptor type-1 in vitro. Eur J Pharmacol. 2013;721(1-3):133–140.

3. Yang Y, Duan W, Lin Y, Yi W, Liang Z, Yan J, Wang N, Deng C, Zhang S, Li Y, Chen W, Yu S, Yi D, Jin Z. SIRT1 activation by curcumin pretreatment attenuates mitochondrial oxidative damage induced by myocardial ischemia reperfusion injury. Free Radic Biol Med. 2013 Dec;65:667-679.

4. Sun Q, Jia N, Wang W, Jin H, Xu J, Hu H. (2014 May) Activation of SIRT1 by curcumin blocks the neurotoxicity of amyloid-β25-35 in rat cortical neurons. Biochem Biophys Res Commun. 448(1):89-94.

5. Sun Y, Hu X, Hu G, Xu C, Jiang H. Curcumin Attenuates Hydrogen Peroxide-Induced Premature Senescence via the Activation of SIRT1 in Human Umbilical Vein Endothelial Cells. Biol Pharm Bull. 2015;38(8):1134-41.

6. Freitas HR, Isaac AR, Malcher-Lopes R, Diaz BL, Trevenzoli IH, De Melo Reis RA. Polyunsaturated fatty acids and endocannabinoids in health and disease. Nutr Neurosci. 2018;21(10):695–714.

Calon F, Cole G. Neuroprotective action of omega-3 polyunsaturated fatty acids against neurodegenerative diseases: evidence from animal studies. Prostaglandins LeukotEssent Fatty Acids. 2007;77: 287–293.

Lafourcade M, Larrieu T, Mato S, Duffaud A, Sepers M, Matias I, et al. Nutritionalomega-3 deficiency abolishes endocannabinoid-mediated neuronal functions. NatNeurosci. 2011;14: 345–350.

Larrieu T, Madore C, Joffre C, Layé S. Nutritional n-3 polyunsaturated fatty acids deficiency alters cannabinoid receptor signaling pathway in the brain and associated anxiety-like behavior in mice. J Physiol Biochem. 2012;68: 671–681.

7. Hayakawa K, Mishima K, Nozako M, Hazekawa M, Aoyama Y, Ogata A, Harada K, Fujioka M, Abe K, Egashira N, Iwasaki K, Fujiwara M. (2007 Mar) High-cholesterol feeding aggravates cerebral infarction via decreasing the CB1 receptor. Neurosci Lett. 414(2):183-7.

8. Diaz-Ruiz, A., Di Francesco, A., Carboneau, B. A., Levan, S. R., Pearson, K. J., Price, N. L., Ward, T. M., Bernier, M., de Cabo, R., & Mercken, E. M. (2019). Benefits of Caloric Restriction in Longevity and Chemical-Induced Tumorigenesis Are Transmitted Independent of NQO1. The journals of gerontology. Series A, Biological sciences and medical sciences, 74(2), 155–162.

9. Yessenkyzy, A., Saliev, T., Zhanaliyeva, M., Masoud, A. R., Umbayev, B., Sergazy, S., Krivykh, E., Gulyayev, A., & Nurgozhin, T. (2020). Polyphenols as Caloric-Restriction Mimetics and Autophagy Inducers in Aging Research. Nutrients, 12(5), 1344.

10. Iside, C., Scafuro, M., Nebbioso, A., & Altucci, L. (2020). SIRT1 Activation by Natural Phytochemicals: An Overview. Frontiers in pharmacology, 11, 1225.

11. Lopez Trinidad, L. M., Martinez, R., Kapravelou, G., Galisteo, M., Aranda, P., Porres, J. M., & Lopez-Jurado, M. (2021). Caloric restriction, physical exercise, and CB1 receptor blockade as an efficient combined strategy for bodyweight control and cardiometabolic status improvement in male rats. Scientific reports, 11(1), 4286.

Endnotes: SIRT1 Cautions

1. Powell, M. J., Casimiro, M. C., Cordon-Cardo, C., He, X., Yeow, W. S., Wang, C., McCue, P. A., McBurney, M. W., & Pestell, R. G. (2011). Disruption of a Sirt1-dependent autophagy checkpoint in the prostate results in prostatic intraepithelial neoplasia lesion formation. Cancer research, 71(3), 964–975.

                  Ming, M., Shea, C. R., Guo, X., Li, X., Soltani, K., Han, W., & He, Y. Y. (2010). Regulation of global genome nucleotide excision repair by SIRT1 through xeroderma pigmentosum C. Proceedings of the National Academy of Sciences of the United States of America, 107(52), 22623–22628.

                  Kang YY, Sun FL, Zhang Y, Wang Z. SIRT1 acts as a potential tumor suppressor in oral squamous cell carcinoma. J Chin Med Assoc. 2018 May;81(5):416-422.

                  Leslie M. (2009). SIRT1 takes down tumors. The Journal of Cell Biology, 185(2), 178.

                  Yeung, F., Hoberg, J. E., Ramsey, C. S., Keller, M. D., Jones, D. R., Frye, R. A., & Mayo, M. W. (2004). Modulation of NF-kappaB-dependent transcription and cell survival by the SIRT1 deacetylase. The EMBO journal, 23(12), 2369–2380.

2. Niederer F, Ospelt C, Brentano F, Hottiger MO, Gay RE, Gay S, Detmar M, Kyburz D. SIRT1 overexpression in the rheumatoid arthritis synovium contributes to proinflammatory cytokine production and apoptosis resistance. Ann Rheum Dis. 2011 Oct;70(10):1866-73.

                  Lin Z, Yang H, Kong Q, Li J, Lee SM, Gao B, Dong H, Wei J, Song J, Zhang DD, Fang D. USP22 antagonizes p53 transcriptional activation by deubiquitinating Sirt1 to suppress cell apoptosis and is required for mouse embryonic development. Mol Cell. 2012 May 25;46(4):484-94.

                  Chen WY, Wang DH, Yen RC, Luo J, Gu W, Baylin SB. Tumor suppressor HIC1 directly regulates SIRT1 to modulate p53-dependent DNA-damage responses. Cell. 2005 Nov 4;123(3):437-48.

3. Lin, Z., & Fang, D. (2013). The Roles of SIRT1 in Cancer. Genes & cancer, 4(3-4), 97–104.

4. Niederer F, Ospelt C, Brentano F, Hottiger MO, Gay RE, Gay S, Detmar M, Kyburz D. SIRT1 overexpression in the rheumatoid arthritis synovium contributes to proinflammatory cytokine production and apoptosis resistance. Ann Rheum Dis. 2011 Oct;70(10):1866-73.

5. Lee, J., You, J. H., Kim, M. S., & Roh, J. L. (2020). Epigenetic reprogramming of epithelial-mesenchymal transition promotes ferroptosis of head and neck cancer. Redox biology, 37, 101697.

Largest ever independent study into cannabis use

Source: BBC.com | Author: BBC | Aug 30, 2022

A £2.5 million study into the effects of cannabis on the brain has been launched by a London university.

The Cannabis & Me study will research environmental and biological factors behind the different effects people experience when using cannabis.

Dr Marta di Forti
Dr Marta di Forti wants to investigate genetic interactions with the drug

King’s College London want 6,000 people to take part in the investigation, which would be the largest independent study of its kind.

Researchers said the funding from the Medical Research Council would help develop greater understanding of the drug, estimated to be used by 200 million people across the world.

More research is needed about how the drug interacts with the brain so doctors can be more confident when considering prescribing medical cannabis, said lead researcher, Dr Di Forti.

“Cannabis is consumed daily by many recreationally but also for medicinal reasons,” she said.

“But in the UK, the prescription of medicinal cannabis remains rare.

“Our study aims to provide data and tools that can make physicians in the UK and across the world more confident, where appropriate, in prescribing cannabis safely.”

The aim is to understand the link between a user’s biological makeup and the effect cannabis has on them.

Cannabis medicine production line
Production of cannabis-infused medicine at the Government Pharmaceutical Organization in Thailand

Researchers will use a combination of virtual reality, psychological and cognitive analysis, and DNA testing.

They will also look at epigenetics in participants, which is how behaviour and environment can impact the way genes work.

Dr Di Forti said she was particularly interested in uncovering any markers connected to potential problems in users, for example mental health or social problems.

The team is now looking for participants between the ages of 18-45 living in the London area, who are either currently using cannabis or have used it less than three times or never before.

The first step for participants is filling out a 40-minute survey online, external.