Modulators of endocannabinoid enzymic hydrolysis and membrane transport

Handb Exp Pharmacol. 2005:(168):187-207. doi: 10.1007/3-540-26573-2_6.

Abstract

Tissue concentrations of the endocannabinoids N-arachidonoylethanolamine (AEA) and 2-arachidonoylglycerol (2-AG) are regulated by both synthesis and inactivation. The purpose of this review is to compile available data regarding three inactivation processes: fatty acid amide hydrolase, monoacylglycerol lipase, and cellular membrane transport. In particular, we have focused on mechanisms by which these processes are modulated. We describe the in vitro and in vivo effects of inhibitors of these processes as well as available evidence regarding their modulation by other factors.

Publication types

  • Review

MeSH terms

  • Amidohydrolases / antagonists & inhibitors
  • Amidohydrolases / physiology
  • Animals
  • Arachidonic Acids / metabolism
  • Biological Transport
  • Cannabinoid Receptor Modulators / metabolism*
  • Cell Membrane / metabolism*
  • Endocannabinoids*
  • Humans
  • Hydrolysis
  • Monoacylglycerol Lipases / antagonists & inhibitors
  • Monoacylglycerol Lipases / physiology
  • Polyunsaturated Alkamides
  • Substrate Specificity

Substances

  • Arachidonic Acids
  • Cannabinoid Receptor Modulators
  • Endocannabinoids
  • Polyunsaturated Alkamides
  • Monoacylglycerol Lipases
  • Amidohydrolases
  • fatty-acid amide hydrolase
  • anandamide