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Mode of regulation by G protein of the ATP-sensitive K+ channel in guinea-pig ventricular cell membrane.

机译:豚鼠心室细胞膜中ATP敏感K +通道的G蛋白调节模式。

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摘要

1. The effect of G protein activation on the ATP-sensitive K+ (K+ATP) channel was examined in inside-out patches from guinea-pig ventricular myocytes. At low (0.3 mM) intracellular ATP concentration ([ATP]i) in the bathing solution, in the absence of agonists in the pipette, guanosine 5'-O-(3-thiotriphosphate) (GTP gamma S) or AlF4- applied to the intracellular side of the patch membrane gradually activated the K+ATP channel. The activation by GTP gamma S was irreversible, although high [ATP]i could completely close the channel. 2. In ATP-free media GTP gamma S did not increase further the activity of the fully active channel, and was unable to reactivate the channel in the non-operative state after rundown. [ATP]i-channel activity curves constructed before and after GTP gamma S application demonstrated that GTP gamma S shifts the half-inhibitory [ATP]i from 19.5 to 110 microM without changing the Hill coefficient. 3. When acetylcholine or adenosine was included in the pipette, intracellular GTP reversibly activated the K+ATP channel which was partially inhibited by [ATP]i. 4. These results indicate that G protein may stimulate myocardial K+ATP channels in the operative state by reducing the potency of ATP inhibition. The possible coupling of the G protein with muscarinic as well as A1 adenosine receptors is suggested.
机译:1.在豚鼠心室肌​​细胞的由内而外的贴片中检查了G蛋白激活对ATP敏感K +(K + ATP)通道的影响。在低浓度(0.3 mM)的沐浴液中细胞内ATP浓度([ATP] i)下,在移液管中不存在激动剂的情况下,将鸟苷5'-O-(3-硫代三磷酸)(GTPγS)或AlF4-应用于膜的细胞内侧逐渐激活K + ATP通道。尽管高[ATP] i可以完全关闭通道,但GTPγS的激活是不可逆的。 2.在无ATP的介质中,GTPγS不会进一步增加完全活动通道的活性,并且在停机后无法在非操作状态下重新激活通道。在应用GTPγS之前和之后构建的[ATP] i通道活性曲线表明,GTPγS将半抑制性[ATP] i从19.5变为110 microM,而没有改变Hill系数。 3.当移液管中包含乙酰胆碱或腺苷时,细胞内GTP可逆地激活K + ATP通道,该通道被[ATP] i部分抑制。 4.这些结果表明,G蛋白可能通过降低ATP抑制的效力而在手术状态下刺激心肌K + ATP通道。建议将G蛋白与毒蕈碱以及A1腺苷受体偶联。

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