It comes as a surprise to many people that we have a system in our bodies capable of producing its own cannabinoids without you ever picking up a hemp or cannabis product. \u00a0According to the <\/span>Journal of Nature Reviews Drug Discovery<\/span><\/a>, the discovery of this system occurred some time in the mid-1990s, after scientists found membrane receptors (known as CB receptors) used by the psychoactive compound delta9-tetrahydrocannabinol or THC. Some scientists thought that THC acted on individual body cells, but this discovery proved that notion wrong. As it is understood now, we wouldn\u2019t actually get \u201chigh\u201d from THC in cannabis plants at all if we did not have an endocannabinoid system. Other species in the world cannot get \u201chigh\u201d because they lack this feature in their anatomy.<\/span><\/p>\n According to the <\/span>Journal of Comparative Neurology<\/span><\/a>, such a system is common in many creatures including in mammals, birds, amphibians, fish, sea urchins, leeches, mussels, and even the most primitive animal with a nerve network, the Hydra. However, the presence of <\/span>CB receptors<\/span><\/a> has not been seen in terrestrial invertebrates (or any member of the Ecdysozoa). Surprisingly, no specific bindings of the synthetic CB ligands [(3)H]CP55,940 and [(3)H]SR141716A were found in a panel of insects: Apis mellifera, Drosophila melanogaster, Gerris marginatus, Spodoptera frugiperda, and Zophobas atratus. <\/span><\/p>\n Another study confirming the endocannabinoid system in humans was one done on runners in 2003. This <\/span>study<\/span><\/a> showed that male college students running on a treadmill or cycling on a stationary bike for 50 minutes had their endocannabinoid system activated. This study was among the first evidence to suggest alternative explanations for exercise\u2019s ability to induce analgesia, or \u201crunner\u2019s high,\u201d in people.<\/span><\/p>\n Other good preliminary knowledge to have before we dive into endogenous cannabinoids is about the four subtypes of receptors in the endocannabinoid system upon which they can act. We usually only talk about two, but these four types are… <\/span><\/p>\n Some might be yet to be discovered, since truncated forms of the CB1 receptor (like CB1A) have also been found.<\/span><\/p>\n Also important is knowing where CB1 and CB2 receptors are generally located. According to an <\/span>article<\/span><\/a> in the Journal of Current Neuropharmacology, \u201cCB1 receptors are abundant and widely dispersed throughout the brain. Their distribution has been mapped by autoradiographic studies, immunohistochemical techniques, in situ histochemistry, and electrophysiological studies. CB1 receptors have shown particularly high levels of expression in cortex, basal ganglia, hippocampus, and cerebellum and low levels of expression in brainstem nuclei.\u201d \u00a0In contrast, CB2 receptors are found mostly on white blood cells and in the spleen. <\/span><\/p>\n First thing to know regarding endogenous cannabinoids is that they are synonymous with endocannabinoids. \u201cEndo\u201d simply means \u201cwithin\u201d or \u201cinternal\u201d while \u201cgenous\u201d comes from the same root word as \u201cgenerate\u201d or \u201cgenesis\u201d – in other words, \u201cmake\u201d or \u201ccreate.\u201d The words \u201cendogenous cannabinoids\u201d and \u201cendocannabinoids\u201d will be used interchangeably. \u00a0Endocannabinoids serve as intercellular “lipid messengers” signaling molecules that are released from one cell and activating the cannabinoid receptors present on other nearby cells. The first endogenous cannabinoid to be isolated and structurally characterized in 1992 was arachidonylethanolamide, commonly known as anandamide, and it was taken from a pig brain.<\/span><\/p>\n Fun fact: The name for this chemical comes from the Sanskrit word ananda, which means \u201cbliss.\u201d This <\/span>study<\/span><\/a> published in the Journal of Neurochemistry shows how anandamide works. Anandamide can bind to membranes in two ways. Either it does this transiently, quickly passing, or it does so when it is \u201ctransfected with an expression plasmid carrying the cannabinoid receptor DNA.\u201d Transfection, in biology terms, is a method of introducing genetic material. An expression plasmid can affect the gene expression in cells. The anandamide also inhibits the forskolin-stimulated adenylate cyclase in the transfected cells. \u00a0What all this means is that \u201canandamide is an endogenous agonist that may serve as a genuine neurotransmitter for the cannabinoid receptor.\u201d Anandamide affects how CB1 receptors do or don\u2019t get activated.<\/span><\/p>\n Anandamide is synthesised by the hydrolysis of the precursor N-arachidonoyl phosphatidylethanolamine, which is catalysed by the enzyme phosphodiesterase phospholipase D. After release from the postsynaptic terminal, which is the receiving part of the connection (synapse) between two nerve cells (neurons), anandamide interacts with presynaptic cannabinoid receptors. Deficiencies can have unpleasant results, as this <\/span>study<\/span><\/a> about neuropathic pain in mice shows. Anandamide plays a role in pain, mood, appetite, and memory and is the most extensively studied endogenous cannabinoid. \u00a0\u00a0\u00a0\u00a0\u00a0\u00a0<\/span><\/p>\n Like anandamide, 2-AG is also an endogenous ligand for CB1 receptors. According to a <\/span>study<\/span><\/a> published in the Journal of Neuroscience, it is the most prevalent endogenous cannabinoid ligand in the brain. The study, which observed self-administered injections of squirrel monkeys, also pointed to data suggesting that 2-AG plays a role in drug-taking behaviors. The monkeys were shown to exhibit an addictive behavior when given 2-AG. Its role in the organism overall is still being established, but recent studies show that it plays a role in the regulation of the circulatory system via direct and\/or indirect effects on blood vessels and\/or heart. It is synthesised by cleavage of an inositol-1,2-diacylglycerol, which is catalysed by phospholipase C.<\/span><\/p>\n This endogenous cannabinoid is a CB1 partial agonist but is a CB1 antagonist in vivo (in the body). It was discovered in June of 2002. Virodhamine is arachidonic acid and ethanolamine joined by an ester linkage. In the hippocampus, its concentrations are similar to those of anandamide. In peripheral tissues that express the CB2 receptor, however, it was found in amounts that were 2- to 9-fold higher than anandamide. <\/span><\/p>\n At the CB2 receptor, it acts as a full agonist. It sometimes can antagonize other endocannabinoids in vivo; for example, it can inhibit anandamide transport. In a <\/span>study<\/span><\/a> published in the British Journal of Pharmacology, it was shown to relax rat mesenteric arteries through endothelial cannabinoid receptors. It can do this to the human pulmonary artery via two mechanisms: It activates the putative endothelial cannabinoid receptor, and it initiates the hydrolysis of virodhamine to arachidonic acid and subsequent production of a vasorelaxant prostanoid through COX. \u00a0<\/span><\/p>\n Here are some things you need to understand about how CBD relates to these endogenous cannabinoids. CBD is not itself an endogenous cannabinoid; however, it acts on CB receptors in a similar manner to some endogenous cannabinoids, like OAE. THC and CBD both influence the way that natural endocannabinoids carry out their jobs. Sometimes, they are agonists in one spot and antagonists for another. <\/span><\/p>\n We hope that this helps clear up some information about the endogenous cannabinoids involved in the endocannabinoid system. It is perhaps commonly thought when hearing about this system that we produce things like CBD in our bodies, but this isn\u2019t quite so. We produce very similar chemicals that do very similar things that also influence how cannabinoids like CBD and THC will interact with our CB receptors or other receptor sites. \u00a0Some are ligands for synaptic reactions, and some are agonists\/antagonists<\/span><\/p>\n\n
Endogenous Cannabinoids – What are these chemicals you make?<\/b><\/h2>\n
Anandamide<\/b><\/h2>\n
2-Arachidonoylglycerol (2-AG)<\/b><\/h2>\n
Virodhamine (OAE)<\/b><\/h2>\n
In Retrospect: Clearing Up Misinformation <\/b><\/h2>\n
In Conclusion..<\/b><\/h2>\n