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在常温条件下,MK-801和戊巴比妥对沙鼠前脑缺血后神经元损伤具有有限但明显的保护作用。

Limited but evident protective effects of MK-801 and pentobarbital on neuronal damage following forebrain ischemia in the gerbil under normothermic conditions.

作者信息

Murase K, Kato H, Kogure K

机构信息

Department of Neurology, Tohoku University School of Medicine, Sendai, Japan.

出版信息

Neurosci Lett. 1993 Jan 12;149(2):229-32. doi: 10.1016/0304-3940(93)90778-j.

Abstract

The purpose of this study was to examine the protective effects of an N-methyl-D-aspartate receptor antagonist, MK-801, and pentobarbital against neuronal damage in a global ischemia model under controlled body temperature. Gerbils were subjected to 3 and 5 min of bilateral common carotid artery occlusion. MK-801 (1 and 5 mg/kg, i.p.), administered 30 min before ischemia, significantly attenuated the degeneration of hippocampal CA1 pyramidal cells after 3 min of ischemia in a dose dependent manner, but had no such effects after 5 min of ischemia. Pentobarbital (40 mg/kg, i.p.) also protected against CA1 damage after 3 min of ischemia but not after 5 min of ischemia. Thus, we confirmed the protective effects of these agents under normothermic conditions, although these effects were limited to shorter periods of ischemia.

摘要

本研究的目的是在体温受控的全脑缺血模型中,检测N-甲基-D-天冬氨酸受体拮抗剂MK-801和戊巴比妥对神经元损伤的保护作用。将沙鼠双侧颈总动脉闭塞3分钟和5分钟。在缺血前30分钟腹腔注射MK-801(1和5mg/kg),能以剂量依赖的方式显著减轻缺血3分钟后海马CA1锥体细胞的变性,但在缺血5分钟后则无此作用。戊巴比妥(40mg/kg,腹腔注射)在缺血3分钟后也能预防CA1损伤,但在缺血5分钟后则不能。因此,我们证实了这些药物在常温条件下的保护作用,尽管这些作用仅限于较短的缺血时间。

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