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单唾液酸神经节苷脂(GM1)可恢复大鼠局灶性皮质缺血后缺血组织中的膜脂肪酸水平。

Monosialoganglioside (GM1) restores membrane fatty acid levels in ischemic tissue after cortical focal ischemia in rat.

作者信息

Mahadik S P, Hungund B L, Gokhale V S, Ortiz A, Makar T K, Karpiak S E

机构信息

Division of Neuroscience, New York State Psychiatric Institute, NY.

出版信息

Neurochem Int. 1993 Aug;23(2):163-72. doi: 10.1016/0197-0186(93)90094-l.

Abstract

Using a consistent, reproducible and reliable cortical focal ischemia in rat (permanent unilateral occlusion of the left middle cerebral artery & the ipsilateral common carotid artery [MCAo + CCAo] with a 1 h temporary occlusion of the contralateral CCA), the levels of four major membrane fatty acids (palmitic, C16:0; stearic, C18:0; Oleic, C18:1 and arachidonic, C20:4) were analyzed at 3, 36 and 72 h, and 2 and 4 wk following ischemia to determine the critical point of irreversibility of the cellular plasma membrane disorganization in primary ischemic (Area 1, parietal cortex) and peri-ischemic (Area 2, tempero-occipital cortex) areas. The cortical focal ischemia resulted in time dependent differential loss in four of these major membrane fatty acids. The quantitative differences among primary and peri-ischemic areas reflected the different degree of ischemic injury inflicted to these regions. Acute treatment with ganglioside GM1 protected the further losses of all of these fatty acids and differentially restored their levels in these various injury sites over periods of time. The changes in levels of these membrane fatty acids indicate that the primary ischemic area suffers an irreversible injury and peri-ischemic area suffers reversible injury. After acute treatment (< 2 h) with ganglioside GM1, a partial recovery was observed in primary ischemic area and complete recovery was observed in peri-ischemic areas. These studies support the hypothesis that, ischemia leads to a irreversible plasma membrane disorganization which underlies the eventual cell death, and protection and restoration of these membrane changes by drugs, such as ganglioside GM1 leads to neuroprotection against ischemic injury.

摘要

利用一种在大鼠中持续、可重复且可靠的皮质局灶性缺血模型(永久性结扎左侧大脑中动脉和同侧颈总动脉[大脑中动脉闭塞+颈总动脉闭塞],同时对侧颈总动脉暂时闭塞1小时),在缺血后3小时、36小时、72小时以及2周和4周时分析四种主要膜脂肪酸(棕榈酸,C16:0;硬脂酸,C18:0;油酸,C18:1;花生四烯酸,C20:4)的水平,以确定原发性缺血区(区域1,顶叶皮质)和缺血周围区(区域2,颞枕叶皮质)细胞膜解体不可逆的关键点。皮质局灶性缺血导致这四种主要膜脂肪酸随时间出现不同程度的损失。原发性缺血区和缺血周围区之间的定量差异反映了这些区域遭受的缺血性损伤程度不同。神经节苷脂GM1的急性治疗可保护所有这些脂肪酸的进一步损失,并在不同时间段内使它们在这些不同损伤部位的水平有差异地恢复。这些膜脂肪酸水平的变化表明,原发性缺血区遭受不可逆损伤,而缺血周围区遭受可逆性损伤。用神经节苷脂GM1进行急性治疗(<2小时)后,在原发性缺血区观察到部分恢复,在缺血周围区观察到完全恢复。这些研究支持以下假设,即缺血导致不可逆的质膜解体,这是最终细胞死亡的基础,而药物(如神经节苷脂GM1)对这些膜变化的保护和恢复可导致对缺血性损伤的神经保护作用。

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