And Now.......Asia

“As the global recognition of the benefits of medical cannabis continues to expand, the thin of the wedge into Asia may well be South Korea. They may be importing cannabis in 2019 already.”

- Dr. David Hepburn

Abstract:

Patients with epilepsy and other rare diseases will be able to get medical marijuana in South Korea as soon as early 2019, the Ministry of Food and Drug Safety said Thursday.

As the National Assembly passed a bill to amend the Act on the Management of Narcotic Drugs on Nov. 23, the sale, import, and export of cannabis for medical purposes will soon become legal.

Read full article here:

http://www.koreaherald.com/view.php?ud=20181129000668

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Dr. Dave Hepburn website: https://doctordavidhepburn.com

Medical Cannabis Laws Decreases violent crime by 20% in California

“Researchers found no influence of the legalisation of cannabis for medicinal purposes in the USA nonviolent property crime at the national level.”

-    Dr. David Hepburn

Abstract:

Most U.S. states have passed medical marijuana laws.

This document presents a study of the effects of these laws on violent and property crime.

It´s interesting to find that in California the medical marijuana law reduced both violent and property crime by 20%.

Read full article here:

https://www.sciencedirect.com/science/article/pii/S016726811830180X?via%3Dihub

Dr. Dave Hepburn website: https://doctordavidhepburn.com

Liverwort As A Legal High - Dr. David Hepburn

"Not only do the various cannabinoids in the cannabis plant act on many different receptors besides our cannabis receptors (CB1R and CB2R) throughout our body, but many other plants produce cannabinomimetics that act on our CB1R and CB2R, in the brain, bones, gut and elsewhere. It’s a busy, complicated network of receptors, ligands and exogenous compounds that are able to have a multitude of effects on our body, some for good and some for.... “good” if you want to be stoned."

-Dr. David Hepburn    

Recommended by Dr. David Hepburn:

Uncovering the psychoactivity of a cannabinoid from liverworts associated with a legal high.

Abstract

Phytochemical studies on the liverwort Radula genus have previously identified the bibenzyl (-)-cis-perrottetinene (cis-PET), which structurally resembles (-)-Δ9-trans-tetrahydrocannabinol (Δ9-trans-THC) from Cannabis sativa L. Radula preparations are sold as cannabinoid-like legal high on the internet, even though pharmacological data are lacking. 

Herein, we describe a versatile total synthesis of (-)-cis-PET and its (-)-trans diastereoisomer and demonstrate that both molecules readily penetrate the brain and induce hypothermia, catalepsy, hypolocomotion, and analgesia in a CB1 receptor-dependent manner in mice. The natural product (-)-cis-PET was profiled on major brain receptors, showing a selective cannabinoid pharmacology. This study also uncovers pharmacological differences between Δ9-THC and PET diastereoisomers. Most notably, (-)-cis-PET and (-)-trans-PET significantly reduced basal brain prostaglandin levels associated with Δ9-trans-THC side effects in a CB1 receptor-dependent manner, thus mimicking the action of the endocannabinoid 2-arachidonoyl glycerol. 

Therefore, the natural product (-)-cis-PET is a psychoactive cannabinoid from bryophytes, illustrating the existence of convergent evolution of bioactive cannabinoids in the plant kingdom. Our findings may have implications for bioprospecting and drug discovery and provide a molecular rationale for the reported effects upon consumption of certain Radula preparations as moderately active legal highs.

To read the full article please visit:

https://www.ncbi.nlm.nih.gov/pubmed/30397641

Dr. Dave Hepburn website:https://doctordavidhepburn.com

Exciting Promise of Role of CBD in Alzheimer’s Neuro-inflammation - Dr. David Hepburn

Article Recommended by Dr. David Hepburn:

"GPR55 is a receptor that is getting a lot of attention in medical research. 40% of drugs are meant to target this receptor due to it’s role in conditions ranging from colon cancer to dementia to MS. THC activates this receptor while CBD does the exact opposite, further underscoring the complicated relationship of the various cannabinoids and showing that “cannabis is not cannabis, it’s cannabis.” The CBD blockage of this receptor is showing promise in addressing certain disease states such as Alzheimers disease, as this recent rat research reveals."

-Dr. Dave Hepburn

Anti-neuroinflammatory effects of GPR55 antagonists in LPS-activated primary microglial cells

Abstract

Background

Neuroinflammation plays a vital role in Alzheimer’s disease and other neurodegenerative conditions. Microglia are the resident mononuclear immune cells of the central nervous system, and they play essential roles in the maintenance of homeostasis and responses to neuroinflammation. The orphan G-protein-coupled receptor 55 (GPR55) has been reported to modulate inflammation and is expressed in immune cells such as monocytes and microglia. However, its effects on neuroinflammation, mainly on the production of members of the arachidonic acid pathway in activated microglia, have not been elucidated in detail.

Methods

In this present study, a series of coumarin derivatives, that exhibit GPR55 antagonism properties, were designed. The effects of these compounds on members of the arachidonic acid cascade were studied in lipopolysaccharide (LPS)-treated primary rat microglia using Western blot, qPCR, and ELISA.

Results

We demonstrate here that the various compounds with GPR55 antagonistic activities significantly inhibited the release of PGE2 in primary microglia. The inhibition of LPS-induced PGE2 release by the most potent candidate KIT 17 was partially dependent on reduced protein synthesis of mPGES-1 and COX-2. KIT 17 did not affect any key enzyme involved on the endocannabinoid system. We furthermore show that microglia expressed GPR55 and that a synthetic antagonist of the GPR receptor (ML193) demonstrated the same effect of the KIT 17 on the inhibition of PGE2.

Conclusions

Our results suggest that KIT 17 is acting as an inverse agonist on GPR55 independent of the endocannabinoid system. Targeting GPR55 might be a new therapeutic option to treat neurodegenerative diseases with a neuroinflammatory background such as Alzheimer’s disease, Parkinson, and multiple sclerosis (MS).

To read the full article please visit:

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240959/ 

Dr. Dave Hepburn website:https://doctordavidhepburn.com