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实验性脑缺血时脑内有机渗透溶质的变化

Changes in brain organic osmolytes in experimental cerebral ischemia.

作者信息

Nonaka M, Yoshimine T, Kohmura E, Wakayama A, Yamashita T, Hayakawa T

机构信息

Department of Neurosurgery, Osaka University Medical School, Suita, Japan.

出版信息

J Neurol Sci. 1998 Apr 15;157(1):25-30. doi: 10.1016/s0022-510x(98)00062-8.

Abstract

The cell volume is regulated not only by inorganic ions, but also by organic osmolytes, such as amino acids, methylamines, and polyhydric alcohols (polyols). Using proton nuclear magnetic resonance spectroscopy (1H-NMR), we measured the tissue concentrations of amino acids (alanine, aspartate, gamma-aminobutyric acid (GABA), glutamate, glutamine, N-acetyl-aspartate (NAA), taurine), methylamines (glycerophosphorylcholine (GPC), creatine+phosphocreatine (total creatine, tCr)), and polyols (myo-inositol) in the rat brain after middle cerebral artery occlusion (incomplete focal ischemia) or after decapitation (complete global ischemia). The total osmolytes expressed as a sum of total amino acids, total methylamines, and total polyols were significantly decreased at 24 h of focal ischemia (58.7% of control value, P=0.0025) whereas they were not changed following decapitation. The water content was increased from control value of 77.9%-84.1% after focal ischemia (P<0.0001) but not after decapitation. These results suggest that the brain organic osmolytes are involved in the process of edema formation following focal cerebral ischemia. Further elucidation of the cellular mechanisms regulating these organic osmolytes in cerebral ischemia may promote greater understanding of the pathophysiology involved in the evolution of brain edema.

摘要

细胞体积不仅受无机离子调节,还受有机渗透溶质调节,如氨基酸、甲胺和多元醇。我们使用质子核磁共振波谱法(1H-NMR),测量了大脑中动脉闭塞(不完全局灶性缺血)或断头(完全性全脑缺血)后大鼠脑中氨基酸(丙氨酸、天冬氨酸、γ-氨基丁酸(GABA)、谷氨酸、谷氨酰胺、N-乙酰天门冬氨酸(NAA)、牛磺酸)、甲胺(甘油磷酸胆碱(GPC)、肌酸+磷酸肌酸(总肌酸,tCr))和多元醇(肌醇)的组织浓度。以总氨基酸、总甲胺和总多元醇之和表示的总渗透溶质在局灶性缺血24小时时显著降低(为对照值的58.7%,P=0.0025),而断头后则无变化。局灶性缺血后水含量从对照值的77.9%增加到84.1%(P<0.0001),但断头后未增加。这些结果表明,脑内有机渗透溶质参与了局灶性脑缺血后水肿形成的过程。进一步阐明脑缺血中调节这些有机渗透溶质的细胞机制,可能有助于更深入地理解脑水肿演变过程中的病理生理学。

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