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Chemical approaches to therapeutically target the metabolism and signaling of the endocannabinoid 2-AG and eicosanoids.

Abstract
The endocannabinoid system, most popularly known as the target of the psychoactive component of marijuana, Δ(9)-tetrahydrocannabinol (THC), is a signaling network that modulates a diverse range of physiological processes including nociception, behavior, cognitive function, appetite, metabolism, motor control, memory formation, and inflammation. While THC and its derivatives have garnered notoriety in the eyes of the public, the endocannabinoid system consists of two endogenous signaling lipids, 2-arachidonoylglycerol (2-AG) and N-arachidonoylethanolamine (anandamide), which activate cannabinoid receptors CB1 and CB2 in the nervous system and peripheral tissues. This review will focus on the recent efforts to chemically manipulate 2-AG signaling through the development of inhibitors of the 2-AG-synthesizing enzyme diacylglycerol lipase (DAGL) or the 2-AG-degrading enzyme monoacylglycerol lipase (MAGL), and assessing the therapeutic potential of DAGL and MAGL inhibitors in pain, inflammation, degenerative diseases, tissue injury, and cancer.
AuthorsRebecca A Kohnz, Daniel K Nomura
JournalChemical Society reviews (Chem Soc Rev) Vol. 43 Issue 19 Pg. 6859-69 (Oct 07 2014) ISSN: 1460-4744 [Electronic] England
PMID24676249 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Review)
Chemical References
  • Arachidonic Acids
  • Eicosanoids
  • Endocannabinoids
  • Enzyme Inhibitors
  • Glycerides
  • Dronabinol
  • glyceryl 2-arachidonate
  • Monoacylglycerol Lipases
  • Lipoprotein Lipase
Topics
  • Animals
  • Arachidonic Acids (chemistry, metabolism)
  • Dronabinol (chemistry, pharmacology, therapeutic use)
  • Eicosanoids (metabolism)
  • Endocannabinoids (chemistry, metabolism)
  • Enzyme Inhibitors (chemistry, pharmacology, therapeutic use)
  • Glycerides (chemistry, metabolism)
  • Humans
  • Lipoprotein Lipase (antagonists & inhibitors, metabolism)
  • Monoacylglycerol Lipases (antagonists & inhibitors, genetics, metabolism)
  • Mood Disorders (drug therapy, metabolism, pathology)
  • Neoplasms (drug therapy, metabolism, pathology)
  • Neurodegenerative Diseases (drug therapy, metabolism, pathology)
  • Pain (drug therapy, metabolism, pathology)
  • Signal Transduction (drug effects)

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