Anandamide, an endogenous cannabinoid, inhibits Shaker-related voltage-gated K+ channels

[摘要] Anandamide has been identified in porcine brain as an endogenous cannabinoid receptor ligand and is believed to be a counterpart to the psychoactive component of marijuana, Delta(9)-tetrahydrocannabinol (Delta(9)-THC). Here we report that anandamide directly inhibits (IC50, 2.7 mu M) Shaker-related Kv1.2 K+ channels that are found ubiquitously in the mammalian brain. Delta(9)-THC also inhibited Kv1.2 channels with comparable potency (IC50, 2.4 mu M), as did several N-acyl-ethanolamides with cannabinoid receptor binding activity. Potassium current inhibition occurred through a pertussis toxin-insensitive mechanism and was not prevented by the cannabinoid receptor antagonist SR141716A. Utilizing excised patches of Kv1.2 channel-rich membrane as a rapid and sensitive bioassay, we found that phospholipase D stimulated the release of an endogenous anandamide-like K+ channel blocker from rat brain slices. Structure-activity studies were consistent with the possibility that the released blocker was either anandamide or another N-acyl-ethanolamide. Copyright (C) 1996 Elsevier Science Ltd

[发布日期] 1996-07-01

[效力级别]  Proceedings Paper

[关键词] fatty acid;N-acyl-ethanolamide;recombinant potassium channel;patch clamp recording