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首页> 外文期刊>Journal of pharmacological sciences. >Acidic Preconditioning Inhibits Na+/H+ and Na+/Ca2+ Exchanger Interaction via PKCε in Guinea-Pig Ventricular Myocytes
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Acidic Preconditioning Inhibits Na+/H+ and Na+/Ca2+ Exchanger Interaction via PKCε in Guinea-Pig Ventricular Myocytes

机译:酸性预处理抑制豚鼠心室肌​​细胞中通过PKCε的Na + / H +和Na + / Ca2 +交换子相互作用。

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References(31) Cited-By(6) An interaction between the Na+/Ca2+ exchanger (NCX) and the Na+/H+ exchanger (NHE) induces reperfusion injury. We investigated the effect of brief repetitive acidosis as acidic preconditioning on NCX and NHE interaction during recovery from acidosis. NCX current with the reversal potential was measured in guinea-pig ventricular myocytes using the whole-cell voltage clamp. The cells were exposed to 5 min of acidosis preceded by two episodes of brief acidosis as acidic preconditioning. Acidosis inhibited NCX current and upon recovery shifted its reversal potential in the negative direction. The shift was prevented by cariporide, but was augmented by a high concentration of phorbol 13-myristate acetate (PMA). Acidic preconditioning prevented the shift, but not in the presence of a selective PKCε inhibitor. A low concentration of PMA, which activates PKCε selectively, prevented the shift, but together with PKCε inhibitor (εV1-2) restored the shift during recovery. 5-Hydroxydecanoate inhibited the effects of acidic preconditioning and those of both low and high concentrations of PMA. The negative shift of NCX reversal potential during recovery from acidosis may be due to [Na+]i accumulation by the NHE. Acidic preconditioning prevented the shift most likely by activating PKCε, which in turn inhibited the NHE. The NHE–NCX interaction may be one of the important end-effectors of preconditioning.
机译:参考文献(31)引用了(6)Na + / Ca2 +交换剂(NCX)和Na + / H +交换剂(NHE)之间的相互作用引起了再灌注损伤。我们调查了短暂重复性酸中毒作为酸性预处理对酸中毒恢复过程中NCX和NHE相互作用的影响。使用全细胞电压钳测量豚鼠心室肌​​细胞中具有逆转电位的NCX电流。将细胞暴露于酸中毒5分钟,然后进行两次短暂的酸中毒作为酸性预处理。酸中毒抑制了NCX电流,一旦恢复,其逆转电位就向负方向移动。这种变化被卡立泊来肽阻止了,但是高浓度的佛波醇13-肉豆蔻酸酯乙酸盐(PMA)加剧了这种变化。酸性预处理可防止这种转变,但在存在选择性PKCε抑制剂的情况下则不能。低浓度的PMA可选择性激活PKCε,阻止了转移,但与PKCε抑制剂(εV1-2)一起在恢复过程中恢复了转移。 5-羟基癸酸酯可抑制酸性预处理以及低浓度和高浓度PMA的影响。从酸中毒恢复期间NCX逆转电位的负移可能归因于NHE积累的[Na +] i。酸性预处理可以通过激活PKCε来阻止这种转变,而PKCε则可以抑制NHE。 NHE-NCX相互作用可能是预处理的重要末端执行器之一。

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