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大鼠心室肌细胞中G蛋白介导的ATP敏感性钾通道与A1受体的偶联

Coupling of ATP-sensitive K+ channels to A1 receptors by G proteins in rat ventricular myocytes.

作者信息

Kirsch G E, Codina J, Birnbaumer L, Brown A M

机构信息

Department of Anesthesiology, Baylor College of Medicine, Houston, Texas 77030.

出版信息

Am J Physiol. 1990 Sep;259(3 Pt 2):H820-6. doi: 10.1152/ajpheart.1990.259.3.H820.

Abstract

ATP-sensitive K+ (K+[ATP]) current is thought to be regulated by GTP-binding proteins (G proteins), but the pathways that couple receptor, G protein, and channel have not been defined. We studied regulation of tolbutamide-sensitive K+[ATP] current in neonatal rat ventricular myocytes. Application of 0.1 mM ATP to the intracellular side of membrane patches reduced K+ [ATP] channel activity, and addition of the nonhydrolyzable GTP analogue guanosine 5'-O-(3-thiotriphosphate) (GTP gamma S) at 0.1 mM restored activity. Application of 0.1 mM intracellular GTP plus 10 microM extracellular adenosine or 100 nM N6-cyclohexyladenosine had the same effect as GTP gamma S; hence K+[ATP] channels may be coupled to adenosine receptors via G proteins. To determine which G protein, we applied G alpha subunits, preactivated with GTP gamma S to the cytoplasmic side of membrane patches, and found that alpha i1, alpha i2, and alpha i3 mimicked the effect of GTP gamma S, but not alpha o or Gs, suggesting that Gi alpha acts via a membrane-delimited pathway. Adenosine receptor coupling may be important for activating K+[ATP] channels in ischemic muscle.

摘要

ATP敏感性钾离子(K⁺[ATP])电流被认为受鸟苷三磷酸结合蛋白(G蛋白)调节,但连接受体、G蛋白和通道的信号通路尚未明确。我们研究了新生大鼠心室肌细胞中甲苯磺丁脲敏感性K⁺[ATP]电流的调节机制。将0.1 mM ATP施加于膜片的胞内侧会降低K⁺[ATP]通道活性,而添加0.1 mM不可水解的GTP类似物鸟苷5'-O-(3-硫代三磷酸)(GTPγS)可恢复活性。施加0.1 mM胞内GTP加10 μM胞外腺苷或100 nM N⁶-环己基腺苷与GTPγS具有相同效果;因此K⁺[ATP]通道可能通过G蛋白与腺苷受体偶联。为确定是哪种G蛋白,我们将用GTPγS预激活的Gα亚基施加于膜片的胞质侧,发现αi1、αi2和αi3模拟了GTPγS的作用,但αo或Gs则不然,这表明Giα通过膜限定途径发挥作用。腺苷受体偶联对于激活缺血肌肉中的K⁺[ATP]通道可能很重要。

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