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British Journal of Pharmacology (2004) 141, 765–774. doi:10.1038/sj.bjp.0705666

The endocannabinoid system: a general view and latest additions

Luciano De Petrocellis1, Maria Grazia Cascio2 and Vincenzo Di Marzo2

  1. 1Endocannabinoid Research Group, Istituto di Chimica Biomolecolare, Consiglio Nazionale delle Ricerche, Via Campi Flegrei 34, Comprensorio Olivetti, Fabbricato 70, 80078 Pozzuoli (Napoli), Italy
  2. 2Endocannabinoid Research Group, Istituto di Chimica Biomolecolare, Consiglio Nazionale delle Ricerche, Via Campi Flegrei 34, Comprensorio Olivetti, Fabbricato 70, 80078 Pozzuoli (Napoli), Italy

Correspondence: Vincenzo Di Marzo, Endocannabinoid Research Group, Istituto di Chimica Biomolecolare, Consiglio Nazionale delle Ricerche, Via Campi Flegrei 34, Comprensorio Olivetti, Fabbricato 70, 80078 Pozzuoli (Napoli), Italy. E-mail: vdimarzo@icmib.na.cnr.it

Received 24 September 2003; Revised 9 October 2003; Accepted 11 December 2003; Published online 26 January 2004.

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Abstract

After the discovery, in the early 1990s, of specific G-protein-coupled receptors for marijuana's psychoactive principle Delta9-tetrahydrocannabinol, the cannabinoid receptors, and of their endogenous agonists, the endocannabinoids, a decade of investigations has greatly enlarged our understanding of this altogether new signalling system. Yet, while the finding of the endocannabinoids resulted in a new effort to reveal the mechanisms regulating their levels in the brain and peripheral organs under physiological and pathological conditions, more endogenous substances with a similar action, and more molecular targets for the previously discovered endogenous ligands, anandamide and 2-arachidonoylglycerol, or for some of their metabolites, were being proposed. As the scenario becomes subsequently more complicated, and the experimental tasks to be accomplished correspondingly more numerous, we briefly review in this article the latest 'additions' to the endocannabinoid system together with earlier breakthroughs that have contributed to our present knowledge of the biochemistry and pharmacology of the endocannabinoids.

Keywords:

Endocannabinoids, cannabinoid, receptor, anandamide, 2-arachidonoylglycerol, vanilloid, phosphatidic

Abbreviations:

AEA, N-arachidonoyl-ethanolamine (anandamide); 2-AG, 2-arachidonoyl-glycerol; 2-AGE, 2-arachidonyl-glyceryl ether (noladin); AMT, anandamide membrane transporter; DAG, diacylglycerol; FAAH, fatty acid amide hydrolase; GPCRs, G-protein-coupled receptors; MAGLs, monoacylglycerol lipase; NADA, N-arachidonoyl-dopamine; NAPE, N-acyl-phosphatidylethanolamines; NAPE-PLD, NAPE-selective PLD; NArPE, N-arachidonoyl-phosphatidylethanolamine; PA, phosphatidic acid; PI, phosphoinositides; PI-PLC, PI-selective phospholipase C; PLD, phospholipase D; sn-1 DAGL, sn-1-selective DAG lipase; THC, (-)-Delta9-tetrahydrocannabinol; TRPV1, transient receptor potential vanilloid type 1 receptor; virhodamine, O-arachidonoyl-ethanolamine

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