The role of GM1 ganglioside in regulating excitatory opioid effects

被引:29
作者
Wu, G
Lu, ZH
Wei, TJ
Howells, RD
Christoffers, K
Ledeen, RW
机构
[1] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Neurosci, Newark, NJ 07103 USA
[2] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Pediat, Newark, NJ 07103 USA
[3] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Biochem & Mol Biol, Newark, NJ 07103 USA
[4] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Physiol & Pharmacol, Newark, NJ 07103 USA
来源
SPHINGOLIPIDS AS SIGNALING MODULATORS IN THE NERVOUS SYSTEM | 1998年 / 845卷
关键词
D O I
10.1111/j.1749-6632.1998.tb09666.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Our studies with cultured cells have provided new insight into the particular role of GM1 in regulating excitatory opioid responses. GM1 is significantly elevated in chronic opioid-treated cells via G(s)/adenylyl cyclase activation. Such GM1 elevation promotes coupling of opioid receptor with G(s), resulting in attenuation of inhibitory opioid effects and induction of a sustained excitatory response. Application of exogenous GM1, but not other gangliosides, induces excitatory opioid responses not only in neurons and neuroblastoma cells that bear intrinsic opioid receptors but also in nonneuronal cells that are transfected with delta-opioid receptor. The latter system provides evidence that allosteric binding of GM1 changes receptor conformation from a G(i)-coupled to a G(s)-coupled mode. This is supported by preliminary experiments with a mutated delta-opioid receptor.
引用
收藏
页码:126 / 138
页数:13
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