THE PERIPHERAL CANNABINOID RECEPTOR - ADENYLATE-CYCLASE INHIBITION AND G-PROTEIN COUPLING

被引:163
|
作者
BAYEWITCH, M
AVIDORREISS, T
LEVY, R
BARG, J
MECHOULAM, R
VOGEL, Z
机构
[1] WEIZMANN INST SCI, DEPT NEUROBIOL, IL-76100 REHOVOT, ISRAEL
[2] THERAPEUT COMMUNITY, ZOHARIM, ISRAEL
[3] HEBREW UNIV JERUSALEM, FAC MED, DEPT NAT PROD, IL-91010 JERUSALEM, ISRAEL
关键词
ADENYLATE CYCLASE; ANANDAMIDE; CANNABINOID RECEPTOR; DELTA(9)-TETRAHYDROCANNABINOL; GTP-BINDING PROTEINS; TRICYCLIC CANNABINOIDS;
D O I
10.1016/0014-5793(95)01207-U
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Two cannabinoid receptors, designated neuronal (or CB1) and peripheral (or CB2), have recently been cloned, Activation of CB1 receptors leads to inhibition of adenylate cyclase and N-type voltage-dependent Ca2+ channels, Here we show, using a CB2 transfected Chinese hamster ovary cell line, that this receptor binds a variety of tricyclic cannabinoid ligands as well. as the endogenous ligand anandamide, Activation of the CB2 receptor by various tricyclic cannabinoids inhibits adenylate cyclase activity and this inhibition is pertussis toxin sensitive indicating that this receptor is coupled to the G(i)/G(o) GTP-binding proteins, Interestingly, contrary to results with CB1, anandamide did not inhibit the CB2 coupled adenylate cyclase activity and Delta(9)-tetrahydrocannabinol had only marginal effects, These results characterize the CB2 receptor as a functional and distinctive member of the cannabinoid receptor family.
引用
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页码:143 / 147
页数:5
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