Cannabinoid receptor stimulation of guanosine-5'-O-(3-[S-35]thio)triphosphate binding in rat brain membranes

被引:90
作者
Selley, DE
Stark, S
Sim, LJ
Childers, SR
机构
[1] WAKE FOREST UNIV,BOWMAN GRAY SCH MED,DEPT PHYSIOL & PHARMACOL,WINSTON SALEM,NC 27157
[2] WAKE FOREST UNIV,BOWMAN GRAY SCH MED,PROGRAM NEUROSCI,WINSTON SALEM,NC 27157
关键词
cannabinoid receptor; GTP gamma S; G-proteins; SR141716A; WIN; 55212-2;
D O I
10.1016/0024-3205(96)00347-5
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Cannabinoid receptors belong to the class of G-protein-coupled receptors which inhibit adenylylcyclase. Coupling of receptors to G-proteins can be assessed by the ability of agonists to stimulate guanosine-5'-O-(3-[S-35]thio)triphosphate ([S-35]GTP gamma S) binding in the presence of excess GDP. The present study examined the effect of cannabinoid agonists on [S-35]GTP gamma S binding in rat brain membranes. Assays were conducted with 0.05 nM [S-35]GTP gamma S, incubated with rat cerebellar membranes, 1-30 mu M GDP and the cannabinoid agonist WIN 55212-2. Results showed that the ability of WIN 55212-2 to stimulate [S-35]GTP gamma S binding increased with increasing concentrations of GDP, with 10-30 mu M GDP providing approximately 150-200% stimulation by the cannabinoid agonist. The pharmacology of cannabinoid agonist stimulation of [S-35]GTP gamma S binding paralleled that of previously reported receptor binding and adenylyl cyclase assays, and agonist stimulation of [S-35]GTP gamma S binding was blocked by the cannabinoid antagonist SR141716A. Brain regional studies revealed widespread stimulation of [S-35]GTP gamma S binding by WIN 55212-2 in a number of brain areas, consistent with in vitro [S-35]GTP gamma S autoradiography. These results demonstrate that [S-35]GTP gamma S binding in the presence of excess GDP is an effective measure of cannabinoid receptor coupling to G-proteins in brain membranes.
引用
收藏
页码:659 / 668
页数:10
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