大麻素受体2型
GPR18
大麻素
大麻素受体
化学
环化酶
受体
G蛋白偶联受体
腺苷酸激酶
G蛋白
生物化学
生物
兴奋剂
作者
Michael Bayewitch,Tomer Avidor‐Reiss,Rivka Levy,Jacob Barg,Raphael Mechoulam,Zvi Vogel
出处
期刊:FEBS Letters
[Wiley]
日期:1995-11-13
卷期号:375 (1-2): 143-147
被引量:208
标识
DOI:10.1016/0014-5793(95)01207-u
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 Ca 2+ 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 0 GTP‐binding proteins. Interestingly, contrary to results with CB1, anandamide did not inhibit the CB2 coupled adenylate cyclase activity and δ 9 ‐tetrahydrocannabinol had only marginal effects. These results characterize the CB2 receptor as a functional and distinctive member of the cannabinoid receptor family.
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