Jakubovicz D E, Grinstein S, Klip A
Division of Neurology, Hospital for Sick Children, Toronto, Ont., Canada.
Brain Res. 1987 Dec 1;435(1-2):138-46. doi: 10.1016/0006-8993(87)91594-0.
Two consequences of cerebral ischemia are cell acidification and cytotoxic edema. To test the possibility that Na+/H+ exchange mediates acid-induced edema, we measured cytoplasmic pH (pHi) and cell volume changes in C6 glioma cells that were artificially acid-loaded using weak electrolytes. pHi was monitored fluorimetrically with 2',7'-bis-(2-carboxyethyl)-5,6-carboxyfluorescein. Upon acidification with sodium propionate, pHi dropped to 6.74 +/- 0.05 (n = 25), and then recovered to levels near the physiological value of 7.23 +/- 0.02 (n = 13). Cell volume, measured by electronic sizing, increased concomitantly by approximately 50% in sodium propionate solution. Both pHi recovery and cell swelling were Na+-dependent, amiloride-sensitive, and inhibited at pHo less than 6.0. These results demonstrate that in vitro: (1) intracellular acidification can lead to cell swelling, and (2) pHi recovery and the concomitant cell swelling are likely mediated by Na+/H+ exchange. These mechanisms may be related to postischemic cytotoxic glial edema.
脑缺血的两个后果是细胞酸化和细胞毒性水肿。为了检验钠氢交换介导酸诱导水肿的可能性,我们测量了用弱电解质人工加载酸的C6胶质瘤细胞的细胞质pH值(pHi)和细胞体积变化。用2',7'-双(2-羧乙基)-5,6-羧基荧光素荧光法监测pHi。用丙酸钠酸化后,pHi降至6.74±0.05(n = 25),然后恢复到接近生理值7.23±0.02(n = 13)的水平。通过电子测量法测量的细胞体积在丙酸钠溶液中相应增加了约50%。pHi恢复和细胞肿胀均依赖于钠,对氨氯地平敏感,且在细胞外pH值小于6.0时受到抑制。这些结果表明,在体外:(1)细胞内酸化可导致细胞肿胀,(2)pHi恢复和伴随的细胞肿胀可能由钠氢交换介导。这些机制可能与缺血后细胞毒性胶质水肿有关。