Ladilov Y V, Siegmund B, Piper H M
Physiologisches Institut, Justus-Liebig-Universität, Giessen, Germany.
Am J Physiol. 1995 Apr;268(4 Pt 2):H1531-9. doi: 10.1152/ajpheart.1995.268.4.H1531.
Effects of Na+/H+ exchange inhibition and cytosolic acidosis on reoxygenated adult rat ventricular cardiomyocytes were investigated. Cells were incubated in anoxic media at pH 6.4 until pCa of < or = 5, intracellular pH (pHi) of 6.5, and cytosolic [Na+] of 50 mM were reached. On reoxygenation, medium pH was changed to 7.4 to activate Na+/H+ exchange. In one group, 20 microM HOE-694, an inhibitor of Na+/H+ exchange, was added. With or without HOE-694, cytosolic Ca2+ and Na+ returned to control levels within 10 min of reoxygenation. In the absence of HOE-694, the pHi renormalized (to 7.2) within 8 min, but irreversible hypercontracture and transient Ca2+ oscillations were observed. In the presence of HOE-694, pHi stayed acidotic (at 6.5), hypercontracture was prevented, and Ca2+ oscillations were attenuated. When the Na+ pump was inhibited with 0.1 mM ouabain, even partial recovery of Ca2+ control became impossible unless HOE-694 was added. Our conclusions are 1) activation of Na+/H+ exchange does not impair recovery of cytosolic Na+ and Ca2+ control unless activity of the sarcolemmal Na+ pump is critically reduced, and 2) due to prolongation of cytosolic acidosis, inhibition of Na+/H+ exchange protects against reoxygenation-induced hypercontracture and cytosolic Ca2+ oscillations.
研究了钠/氢交换抑制和胞浆酸中毒对再氧合成年大鼠心室心肌细胞的影响。将细胞置于pH 6.4的缺氧培养基中孵育,直至达到pCa≤5、细胞内pH(pHi)为6.5和胞浆[Na⁺]为50 mM。再氧合时,将培养基pH改为7.4以激活钠/氢交换。在一组中,加入20 μM HOE - 694(一种钠/氢交换抑制剂)。无论有无HOE - 694,再氧合10分钟内胞浆Ca²⁺和Na⁺均恢复到对照水平。在无HOE - 694时,pHi在8分钟内恢复正常(至7.2),但观察到不可逆的超收缩和短暂的Ca²⁺振荡。存在HOE - 694时,pHi保持酸中毒状态(在6.5),超收缩得到预防,Ca²⁺振荡减弱。当用0.1 mM哇巴因抑制钠泵时,除非加入HOE - 694,否则Ca²⁺控制即使部分恢复也变得不可能。我们的结论是:1)除非肌膜钠泵活性严重降低,钠/氢交换的激活不会损害胞浆Na⁺和Ca²⁺控制的恢复;2)由于胞浆酸中毒的延长,钠/氢交换的抑制可防止再氧合诱导的超收缩和胞浆Ca²⁺振荡。