Issue: The brain has at least 2 receptors for marijuana and at least 1 naturally occurring ligand, which may be the brain's own marijuana.

The brain makes its own morphine, so why not its own marijuana? Marijuana has been in use for over 4000 years as both a therapeutic agent and a recreational drug. Until 10 years ago, however, the exact mechanism of marijuana's psychoactive properties was relatively obscure, even though the psychoactive ingredient has long been known to be delta-9-tetrahydrocannabinol (THC).Analogous to how the endogenous opiates were discovered, isolation and characterization of cannabinoid (CB) receptors provided the key for their use as a tool in isolating an endogenous ligand for marijuana receptors in the brain.This endogenous ligand is called anandamide.

Marijuana Receptors

So far, 2 CB receptors have been identified, 1 in brain and the other in the immune system.THC binds to at least 2 distinct receptors: CB1 (and another possible subtype called CBlA) and CB2. CB1 receptors are found in highest concentration in brain neurons, are coupled via G proteins, and modulate adenylate cyclase and ion channels. CB2 receptors are found in cells of the immune system, are also coupled via G proteins, but inhibit adenylate cyclase.

Brain Cannabinoid Receptors

Not surprisingly, brain CB1 receptors are thought to mediate reinforcement and reward. They may not only be involved in the mediation of marijuana's reinforcing properties, but also may impact ethanol's reinforcing properties, since the CB1 selective antagonist SR141716A reduces ethanol intake in rats.

The pharmacologic activity of cannabinoids may be partially mediated through 5-HT receptors. Cannabinoids also regulate mesolimbic dopamine transmission, which affects the dopamine "pleasure pathway" and may help to explain the reinforcing properties of marijuana, especially since this mechanism seems to serve as a final common pathway for nearly all drugs of abuse, including nicotine, alcohol, stimulants, and marijuana.

Studies of CB1 receptors in experimental animals exposed to chronic cannabinoids are beginning to explore issues of tolerance, dependence, and withdrawal. Although it is clear that acute administration of marijuana to humans produces intoxication with euphoria, there is a relative absence of acute withdrawal signs typical for other drugs of abuse. This lack of withdrawal symptoms may occur because cannabinoids are stored in body lipids and slowly released into the blood after self-administration has ceased. Presumably, the CB1 receptors that undergo adaptation during acute drug administration have time to readapt by the time the residual drug leaking out of body lipids is all gone.

In terms of chronic administration of marijuana in humans, tolerance to cannabinoids has been well established, but the question of cannabinoid dependence has always been very controversial. The discovery of the CB1 antagonist SR141716A has settled this controversy because it precipitates a withdrawal syndrome in mice chronically exposed to THC. It is therefore likely, but not yet proved, that dependence also occurs in humans, presumably due to the same types of adaptive changes in cannabinoid receptors that occur in other neurotransmitter receptors after chronic administration of other drugs of abuse.

Peripheral Cannabinoid Receptors

Actions of cannabinoids at peripheral cannabinoid receptors may explain altered immune function after long-term cannabinoid administration. Cannabinoids acting at CB2 receptors in the immune system cause inhibition of T-cell-dependent humoral immune responses through direct inhibition of accessory T-cell function. These and other types of signaling events observed in leukocytes responding to cannabinoids that bind to leukocyte CB2 receptors provide interesting insights into how genes may be modulated in cell types other than neurons.
Anandamide, The Brain's Own Marijuana

Anandamide is a member of a family of fatty acid ethanolamides that may represent a novel class of naturally occurring lipid neurotransmitters. Anandamide shares most but not all of the pharmacologic properties of THC. For instance, anandamide's actions at CB1 receptors are mimicked not only by THC, but also by a recently discovered synthetic agonist, CP55-940 and its activities at CB1 receptors are antagonized in part by the selective CB1 antagonist SR141716A.

The discovery of SR141716A opens the door to using this drug as a tool for determining the biological function of CB1 receptors in the human CNS. It may certainly lead to a role in preventing various types of drug abuse, in treating various types of drug dependence, and in reducing symptoms in various disorders hypothesized to be the result of a defect in the mesolimbic dopamine system, such as schizophrenia.

Author: Stephen M. Stahl, M.D., Ph.D.

Researchers say a new animal study shows that cannabinoid receptor sites in the brain also seem to stimulate the reward and pleasure responses to alcohol, the Ascribe Newswire reported Sept. 7.

Scientists at Brookhaven National Laboratory said the study supports the theory that alcoholism susceptibility may have a genetic basis. "These findings build on our understanding of how various receptors in the brain's reward circuits contribute to alcohol abuse, help us understand the role of genetic susceptibility, and move us farther along the path toward successful treatments," said Brookhaven's Panayotis Thanos, lead author of the study.

The study focused on the CB1 receptors in the brains of mice; those with the receptors showed a stronger preference for alcohol than those who had diminished or missing CB1 function. When mice with normal or diminished CB1 receptors had those receptor sites chemically blocked, they drank less alcohol than before, while the mice who never had active CB1 sites did not change their behavior.

Mice with the normal CB1 receptors also spent more time seeking alcohol than those without the receptors. "These results support our belief that the cannabinoid system and CB1 receptors play a critical role in mediating the rewarding and pleasurable properties of alcohol, contributing to alcohol dependency and abuse," Thanos said.

The research was published in Sept. 2, 2005 in the online edition of the journal Behavioural Brain Research.

Source: Join Together

Sorry But I don't get what this is saying.

More and more information and studies are being made into marijuana and associating its use with the onset of psychological disorders and paranoia.

The brain makes its own hormones, but does not make direct copies of herbal or synthetic drugs.

If our knowledge was that advanced and our medicine that perfect, we would be far further ahead in treatment than we are.

Thanks Carp
I have heard about what it could do after an ambo came & did a talk while I was studying. Pretty scary stuff.