Kempski O, Staub F, von Rosen F, Zimmer M, Neu A, Baethmann A
Institute of Surgical Research, Ludwig-Maximilians University, München, FRG.
Neurochem Pathol. 1988 Jul-Dec;9:109-25. doi: 10.1007/BF03160357.
The pathophysiological chain of events occurring during cerebral ischemia is still poorly understood on a molecular level. Therefore, an in vitro model to study glial swelling mechanisms, using C6 glial cells under controlled extracellular conditions, has been established. Flow cytometry serves to determine even small cell volume changes. In this report, the effects of anoxia and acidosis on glial swelling are summarized. Anoxia alone, or in combination with iodoacetate to inhibit anaerobic glycolysis, did not cause an increase of glial volume for up to 2 h. Acidification of the incubation medium below pH 6.8, on the other hand, was immediately followed by cell swelling to 115% of normal. Amiloride or the absence of bicarbonate and Na+ in the medium significantly reduced glial swelling. The data support the contention that swelling results from an activation of the Na+/H+-antiporter to control intracellular pH. It is suggested that swelling in an ischemic penumbra is promoted by this mechanism. Therapeutic approaches to control cerebral pH might be useful to protect brain tissue in cerebral ischemia.
在分子水平上,人们对脑缺血期间发生的病理生理事件链仍知之甚少。因此,已建立了一种体外模型,在可控的细胞外条件下使用C6胶质细胞来研究胶质细胞肿胀机制。流式细胞术可用于确定即使是很小的细胞体积变化。在本报告中,总结了缺氧和酸中毒对胶质细胞肿胀的影响。单独缺氧或与碘乙酸联合使用以抑制无氧糖酵解,在长达2小时内均未导致胶质细胞体积增加。另一方面,将孵育培养基酸化至pH 6.8以下后,细胞立即肿胀至正常体积的115%。氨氯地平或培养基中缺乏碳酸氢盐和Na+可显著减轻胶质细胞肿胀。这些数据支持了肿胀是由Na+/H+反向转运体激活以控制细胞内pH所导致的观点。有人提出,这种机制促进了缺血半暗带中的肿胀。控制脑pH的治疗方法可能有助于保护脑缺血中的脑组织。