Posted On: 03/05/2015 12:46:49 PM
Post# of 1040
Future Neurology
Cannabinoids for the Treatment of Neuropathic Pain
The isolation of Δ9-tetrahydrocannabinol (THC), the major psychoactive ingredient in cannabis, set the stage for the discovery of an endogenous cannabinoid (endocannabinoid) transmitter system.[1] Endogenous signaling molecules for this system were subsequently isolated.[2,3] Anandamide[4] and 2-arachidonoylglycerol (2-AG),[2,3] the best characterized endocannabinoids isolated to date, bind to and activate cannabinoid CB1 and CB2 receptors. CB1 is the primary cannabinoid receptor found in the CNS,[5] whereas CB2 is predominantly, but not exclusively, found in the immune system.[6–8] The discovery of cannabinoid receptors allowed researchers to synthesize cannabinoids and characterize their pain-relieving properties. Anandamide and 2-AG are degraded by the enzymes fatty-acid amide hydrolase and monoacylglycerol lipase,[9] respectively. Enzymes catalyzing endocannabinoid breakdown also represent targets for analgesic drug development. This article will briefly summarize the findings of preclinical and clinical studies evaluating the therapeutic and side-effect profile of cannabinoids as pharmacotherapies for neuropathic pain......................>>>>>>>>>
http://www.medscape.com/viewarticle/739103
Cannabinoids for the Treatment of Neuropathic Pain
The isolation of Δ9-tetrahydrocannabinol (THC), the major psychoactive ingredient in cannabis, set the stage for the discovery of an endogenous cannabinoid (endocannabinoid) transmitter system.[1] Endogenous signaling molecules for this system were subsequently isolated.[2,3] Anandamide[4] and 2-arachidonoylglycerol (2-AG),[2,3] the best characterized endocannabinoids isolated to date, bind to and activate cannabinoid CB1 and CB2 receptors. CB1 is the primary cannabinoid receptor found in the CNS,[5] whereas CB2 is predominantly, but not exclusively, found in the immune system.[6–8] The discovery of cannabinoid receptors allowed researchers to synthesize cannabinoids and characterize their pain-relieving properties. Anandamide and 2-AG are degraded by the enzymes fatty-acid amide hydrolase and monoacylglycerol lipase,[9] respectively. Enzymes catalyzing endocannabinoid breakdown also represent targets for analgesic drug development. This article will briefly summarize the findings of preclinical and clinical studies evaluating the therapeutic and side-effect profile of cannabinoids as pharmacotherapies for neuropathic pain......................>>>>>>>>>
Quote:
Identification of alternative therapeutics that provide adequate pain relief in the absence of adverse side effects remains a strong clinical need.
http://www.medscape.com/viewarticle/739103
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