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酸中毒时胶质细胞肿胀的分子机制。

Molecular mechanisms of glial cell swelling in acidosis.

作者信息

Kempski O, Staub F, Jansen M, Baethmann A

机构信息

Institute for Surgical Research, Ludwig-Maximilians University of Munich, Federal Republic of Germany.

出版信息

Adv Neurol. 1990;52:39-45.

PMID:2168665
Abstract

The mechanism of glial swelling in acidosis were investigated in an in vitro model. C6 glial cells were exposed to pH levels between 7.4 and 6.2. The cell volume response was determined by flow cytometry. Cell swelling of 110% to 115% was observed if pH was reduced to 6.8 or below. This effect was independent of the length of exposure to acidosis. Swelling induced by pH could be attenuated by (a) inhibition of the Na+/H+ antiporter by amiloride, (b) replacement of bicarbonate by HEPES, and (c) inhibition of carbonic anhydrase by acetazolamide. Absence of Na+ ions from the incubation medium completely prevented acidosis-induced glial swelling. Inhibition of the Cl-/HCO3- antiporter reduced swelling only in its first phase. The results suggest that glial swelling in acidosis may be from an activation of anion and cation antiporters as an attempt to maintain a normal intracellular pH. It is concluded that swelling of glial cells in the ischemic penumbra zone evolves along similar mechanisms.

摘要

在体外模型中研究了酸中毒时神经胶质细胞肿胀的机制。将C6神经胶质细胞暴露于pH值在7.4至6.2之间的环境中。通过流式细胞术测定细胞体积反应。如果pH值降至6.8或更低,可观察到细胞肿胀达110%至115%。这种效应与酸中毒暴露时间长短无关。pH诱导的肿胀可通过以下方式减弱:(a) 用氨氯吡咪抑制Na+/H+反向转运体;(b) 用HEPES替代碳酸氢盐;(c) 用乙酰唑胺抑制碳酸酐酶。孵育培养基中缺乏Na+离子可完全阻止酸中毒诱导的神经胶质细胞肿胀。抑制Cl-/HCO3-反向转运体仅在其第一阶段减轻肿胀。结果表明,酸中毒时神经胶质细胞肿胀可能源于阴离子和阳离子反向转运体的激活,作为维持正常细胞内pH值的一种尝试。得出的结论是,缺血半暗带区域神经胶质细胞的肿胀沿类似机制发展。

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