Serotonin and protein kinase C modulation of a rat brain inwardly rectifying K+ channel expressed in Xenopus oocytes

被引:17
作者
DiMagno, L
Dascal, N
Davidson, N
Lester, HA
Schreibmayer, W
机构
[1] GRAZ UNIV, INST MED PHYS & BIOPHYS, A-8010 GRAZ, AUSTRIA
[2] CALTECH, DIV BIOL, PASADENA, CA 91125 USA
[3] TEL AVIV UNIV, SACKLER SCH MED, DEPT PHYSIOL & PHARMACOL, IL-69978 RAMAT AVIV, ISRAEL
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 1996年 / 431卷 / 03期
关键词
serotonin; inward rectifying potassium channel; brain; PKC; 5-HT2C receptor; heterologous expression; Xenopus laevis oocytes; modulation;
D O I
10.1007/BF02207270
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
In Xenopus laevis oocytes injected with rat brain poly(A)(+) RNA, perfusion with a high-K+ solution (96 mM KCl) generated an inward current (I-HK) which was absent in water-injected oocytes. Part of I-HK was blocked by low concentrations of Ba2+ (half-maximal inhibitory concentration, IC50: 4.2 +/- 0.5 mu M). When serotonin (5-HT) was applied to these oocytes a transient inward oscillating Cl- current arising from activation of Ca2+-dependent Cl- channels, I-Cl(Ca), was observed. When this response decayed, a 30% reduction of I-HK could be detected. Electrophysiological characterization of the K+ channel down-modulated by 5-HT revealed that it is an inward rectifier. Antisense suppression experiments revealed that the 5-HT2C receptor mediates the down-modulatory effect of 5-HT. The nature of the modulatory pathway was investigated by application of phorbol esters and intracellular injection of protein kinase C (PKC) inhibitors, ethylenebis (oxonitrilo)tetraacetate (EGTA) and inositol 1, 4, 5-trisphosphate. The results demonstrate that PKC is responsible for the down-modulatory effect.
引用
收藏
页码:335 / 340
页数:6
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