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培养的心脏细胞在pH变化过程中钙通量和收缩状态的改变。

Altered Ca fluxes and contractile state during pH changes in cultured heart cells.

作者信息

Kim D, Smith T W

出版信息

Am J Physiol. 1987 Jul;253(1 Pt 1):C137-46. doi: 10.1152/ajpcell.1987.253.1.C137.

Abstract

We studied mechanisms underlying changes in myocardial contractile state produced by intracellular (pHi) or extracellular (pHo) changes in pH using cultured chick embryo ventricular cells. A change in pHo of HEPES-buffered medium from 7.4 to 6.0 or to 8.8 changed the amplitude of cell motion by -85 or +60%, and 45Ca uptake at 10 s by -29 or +22%, respectively. The pHo-induced change in Ca uptake was not sensitive to nifedipine (10 microM), but was Na gradient dependent. Changes in pHi produced by NH4Cl or preincubation in media at pH values ranging from 6.0 to 8.8 failed to alter significantly 45Ca uptake or efflux. However, larger changes in pHi were associated with altered Ca uptake. Changes in pHo from 7.4 to 6.0 or to 8.8 were associated with initial changes in 45Ca efflux by +17 or -18%, respectively, and these effects were not Na dependent. Exposure of cells to 20 mM NH4Cl produced intracellular alkalinization and a positive inotropic effect, whereas subsequent removal of NH4Cl caused intracellular acidification and a negative inotropic effect. There was, however, a lack of close temporal relationship between pHi and contractile state. These results indicate that pHo-induced changes in contractile state in cultured heart cells are closely correlated with altered transsarcolemmal Ca movements and presumably are due (at least in part) to these Ca flux changes. In contrast, pHi-induced changes in contractile state appear principally to involve altered Ca handling within the cell and/or altered Ca sensitivity of myofibrils.

摘要

我们使用培养的鸡胚心室细胞研究了细胞内(pHi)或细胞外(pHo)pH值变化引起心肌收缩状态改变的潜在机制。HEPES缓冲培养基的pHo从7.4变为6.0或8.8,细胞运动幅度分别改变了-85%或+60%,10秒时的45Ca摄取量分别改变了-29%或+22%。pHo诱导的钙摄取变化对硝苯地平(10 microM)不敏感,但依赖于钠梯度。氯化铵或在pH值为6.0至8.8的培养基中预孵育引起的pHi变化未能显著改变45Ca摄取或流出。然而,pHi的较大变化与钙摄取改变有关。pHo从7.4变为6.0或8.8分别与45Ca流出的初始变化+17%或-18%有关,且这些效应不依赖于钠。将细胞暴露于20 mM氯化铵会导致细胞内碱化和正性肌力作用,而随后去除氯化铵会导致细胞内酸化和负性肌力作用。然而,pHi与收缩状态之间缺乏紧密的时间关系。这些结果表明,pHo诱导的培养心脏细胞收缩状态变化与跨肌膜钙运动改变密切相关,可能(至少部分)归因于这些钙通量变化。相比之下,pHi诱导的收缩状态变化似乎主要涉及细胞内钙处理的改变和/或肌原纤维钙敏感性的改变。

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