CANNABINOID AGONISTS INHIBIT THE ACTIVATION OF 5-HT3 RECEPTORS IN RAT NODOSE GANGLION NEURONS

被引:144
作者
FAN, P
机构
[1] Molecular/Cellular Neurobiology Lab., NIAAA, National Institutes of Health, Rockville, MD 20852
关键词
D O I
10.1152/jn.1995.73.2.907
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
1. Effects of cannabinoid agonists on the serotonin (5-HT)(3) receptor-mediated current were investigated in rat nodose ganglion neurons. Anandamide. Win 55212-2, and CP55940 inhibitid the 5-HT-induced current in a concentration dependent manner. IC50 values were 190, 310, and 94 nM for anandamide. Win 55212-2, and CP55940, respectively, and 1.6 mu M for the nonpsychoactive enantiomer CP56667. This inhibition was slowly developing, noncompetitive, not dependent on membrane potential, and not affected by adenosine 3'.5'-cyclic monophosphate(cAMP) analogues. guanosine-5'-O-(2-thiodiphosphate) (GDP-beta-S), and opioid receptor antagonist naltrexone. These data suggest that 5-HT3 receptor ion-channel is a site acted upon by cannabinoid agonists in the nervous system, and the action of cannabinoid agonists on 5-HT3 receptors may be a possible mechanism for some of the behavioral effects of cannabinoids, such as antiemesis and analgesia.
引用
收藏
页码:907 / 910
页数:4
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