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The regulation of ATP-sensitive K+ channel activity in intact and permeabilized rat ventricular myocytes.

机译:完整和透化的大鼠心室肌细胞中ATP敏感性K +通道活性的调节。

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摘要

1. In isolated rat heart ventricular myocytes exposed to 2 mM-cyanide in the presence of 10 mM-2-deoxyglucose (complete metabolic blockade), there is a time-dependent increase in ATP-sensitive potassium (KATP) channel activity. The increase in KATP channel activity accompanies the decline of twitch amplitude. Channel activation and decline of the twitch amplitude precede the development of a 'rigor' contracture. 2. We measured KATP channel activity in permeabilized cells using the open-cell attached (O-C-A) patch configuration (by establishing a cell-attached patch and then permeabilizing the cell by exposure to saponin). The apparent ATP dependence of KATP channel activity could be described by a sigmoid curve with ki, ATP (ATP concentration required for half-maximum inhibition of channel activity) = 122 microM and H (Hill coefficient) = 1.225. 3. In the O-C-A patch configuration, 10 mM-creatine phosphate (CrP) decreased the apparent ki, ATP from 122 microM to about 10 microM, and the maximal activity (in zero ATP) was decreased to about 30% of the maximal activity in the absence of CrP. 4. In isolated inside-out (I-O) patches, ATP inhibited KATP channel activity at much lower [ATP] than in the O-C-A patch configuration (ki, ATP = 25 microM, H = 2). CrP was without effect on I-O patches. 5. These results are consistent with the hypothesis that the difference in the ATP dependence of KATP channel activity in the O-C-A and I-O patch configurations arises because of ATP consumption in the O-C-A patch configuration. The results suggest that hydrolysis of ATP to ADP by endogenous ATPases leads to the development of gradients of [ATP] and [ADP] between the bath and the 'inside' of the open cell. By re-phosphorylating ADP, CrP is able to dissipate these gradients, revealing the 'true' ATP dependence of channel activity, which is the same as that in the I-O patch configuration. 6. In order to estimate the contribution of KATP channel activity to the rat cardiac action potential at different [ATP] we have made the following measurements. Using electrodes of resistance 2-8 M omega the density of KATP channels was 10.3 +/- 0.1 channels per patch (n = 162).(ABSTRACT TRUNCATED AT 400 WORDS)
机译:1.在存在10 mM-2-脱氧葡萄糖(完全代谢阻断)的情况下,暴露于2 mM氰化物的分离的大鼠心脏心室心肌细胞中,ATP敏感性钾(KATP)通道活性随时间增加。 KATP通道活性的增加伴随着抽搐幅度的下降。通道激活和抽搐幅度下降先于“严格”挛缩的发展。 2.我们使用开孔贴附(O-C-A)贴片配置(通过建立细胞贴附的贴片,然后通过暴露于皂苷来透化细胞)来测量透化细胞中的KATP通道活性。 KATP通道活性的明显ATP依赖性可以通过S型曲线描述,Ki,ATP(通道活性的一半最大抑制所需的ATP浓度)= 122 microM,H(希尔系数)= 1.225。 3.在OCA贴片配置中,10 mM磷酸肌酸(CrP)使表观ki,ATP从122 microM降低到约10 microM,最大活性(零ATP)降低到最大活性的30%。不含CrP。 4.在孤立的由内而外(I-O)补丁中,ATP抑制KATP通道活性的[ATP]远低于O-C-A补丁配置(ki,ATP = 25 microM,H = 2)。 CrP对I-O斑片没有影响。 5.这些结果与以下假设一致:在O-C-A和I-O贴片配置中,KATP通道活性的ATP依赖性的差异是由于O-C-A贴片配置中的ATP消耗引起的。结果表明,内源性ATP酶将ATP水解为ADP会导致浴液和开放细胞“内部”之间[ATP]和[ADP]梯度的发展。通过重新磷酸化ADP,CrP能够消除这些梯度,从而揭示通道活性的“真正” ATP依赖性,这与I-O贴片配置中的相同。 6.为了评估KATP通道活性在不同[ATP]下对大鼠心脏动作电位的贡献,我们进行了以下测量。使用2-8 MΩ电阻的电极,每个贴片的KATP通道密度为10.3 +/- 0.1通道(n = 162)。(以400字截短的抽象截断值)

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