The recent progress in research on effects of anesthetics and analgesics on G protein-coupled receptors

被引:17
作者
Minami, Kouichiro [1 ,2 ]
Uezono, Yasuhito [1 ]
机构
[1] Natl Canc Ctr, Res Inst, Canc Pathophysiol Div, Tokyo 1040045, Japan
[2] Jichi Med Univ, Dept Anesthesiol & Crit Care Med, Shimotsuke, Tochigi 3290483, Japan
关键词
Anesthetics; Analgesics; G protein-coupled receptor; METABOTROPIC GLUTAMATE-RECEPTOR; MU-OPIOID RECEPTOR; MUSCARINIC ACETYLCHOLINE-RECEPTORS; RECTIFYING POTASSIUM CHANNELS; LONG-TERM POTENTIATION; EXPRESSING CLONED M-1; O-DESMETHYL TRAMADOL; XENOPUS-OOCYTES; INDUCED RESPONSES; MICE LACKING;
D O I
10.1007/s00540-012-1507-2
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
The exact mechanisms of action behind anesthetics and analgesics are still unclear. Much attention was focused on ion channels in the central nervous system as targets for anesthetics and analgesics in the 1980s. During the 1990s, major advances were made in our understanding of the physiology and pharmacology of G protein coupled receptor (GPCR) signaling. Thus, several lines of studies have shown that G protein coupled receptors (GPCRs) are one of the targets for anesthetics and analgesics and especially, that some of them inhibit the functions of GPCRs, i.e,, muscarinic receptors and substance P receptors. However, these studies had been focused on only G(q) coupled receptors. There has been little work on G(s)- and G(i)-coupled receptors. In the last decade, a new assay system, using chimera G(i/o)-coupled receptor fused to Gq(i5), has been established and the effects of anesthetics and analgesics on the function of G(i)-coupled receptors is now more easily studied. This review highlights the recent progress of the studies regarding the effects of anesthetics and analgesics on GPCRs.
引用
收藏
页码:284 / 292
页数:9
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