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钠/氢交换依赖的细胞容积与pH调节及紊乱

Na/H exchange-dependent cell volume and pH regulation and disturbances.

作者信息

Cala P M, Anderson S E, Cragoe E J

机构信息

Department of Human Physiology, School of Medicine, University of California, Davis 95616.

出版信息

Comp Biochem Physiol A Comp Physiol. 1988;90(4):551-5. doi: 10.1016/0300-9629(88)90666-4.

Abstract
  1. The role of Na/H exchange in cell volume and pH regulation is discussed. In addition the roles of Cl/HCO3 exchange and system buffers are evaluated as they relate to Na/H exchange-dependent changes in cell salt and water content and intracellular pH. 2. Data obtained from studies of Amphiuma red blood cells showed that in addition to previously reported Na/H exchange dependent volume regulation the pathway is also involved in regulating cell pH. 3. These data showed that in contrast to volume activated Na/H exchange, when the pathway is pH activated it does not deactivate as a function of cell volume. 4. Given what appeared to be mutually exclusive volume and pH regulatory functions of the Na/H exchange, we hypothesized that the pathway might play a role in hypoxic cell swelling (cytotoxic edema). 5. In studies performed on perfused rabbit hearts employing 23Na NMR we were able to observe that relative to normoxic controls hypoxic hearts exhibited a five-fold increase in intracellular Na content when the Na-K pump was inhibited by ouabain and/or K-free perfusate. 6. These studies lead us to conclude that hypoxia-induced Na uptake is the result of an increased inward Na leak as opposed to decreased Na pumping. 7. Based upon studies with a variety of inhibitors of dissipative Na transport, we conclude that the increased inward Na leak in hypoxic hearts is via Na/H exchange.
摘要
  1. 讨论了钠/氢交换在细胞体积和pH调节中的作用。此外,还评估了氯/碳酸氢根交换和系统缓冲剂的作用,因为它们与钠/氢交换依赖性细胞盐和水含量变化以及细胞内pH值有关。2. 从美洲鳗红细胞研究中获得的数据表明,除了先前报道的钠/氢交换依赖性体积调节外,该途径还参与调节细胞pH值。3. 这些数据表明,与体积激活的钠/氢交换相反,当该途径被pH激活时,它不会随细胞体积而失活。4. 鉴于钠/氢交换的体积调节和pH调节功能似乎相互排斥,我们推测该途径可能在缺氧性细胞肿胀(细胞毒性水肿)中起作用。5. 在使用23Na NMR对灌注兔心脏进行的研究中,我们能够观察到,相对于常氧对照组,当钠钾泵被哇巴因和/或无钾灌注液抑制时,缺氧心脏的细胞内钠含量增加了五倍。6. 这些研究使我们得出结论,缺氧诱导的钠摄取是内向钠泄漏增加的结果,而不是钠泵浦减少的结果。7. 根据对各种耗散性钠转运抑制剂的研究,我们得出结论,缺氧心脏内向钠泄漏增加是通过钠/氢交换实现的。

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