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新型认知增强剂奈非西坦对脑栓塞大鼠的影响。

Effects of the new cognition-enhancing agent nefiracetam in rats with cerebral embolism.

作者信息

Tanaka S, Watabe S, Kakihata K, Sakurai T, Endo W, Yamaguchi H, Ashida S

机构信息

Exploratory Research Laboratories II, Daiichi Pharmaceutical Co., Ltd., Tokyo, Japan.

出版信息

Arzneimittelforschung. 1992 Nov;42(11):1274-8.

PMID:1492838
Abstract

The effects of nefiracetam (DM-9384, CAS 77191-36-7) on the learning behavior and cholinergic and GABAergic neuronal transmitter systems of rats with experimentally-induced cerebral embolism were investigated. Cerebral embolisms were induced in male Wistar rats by injection of 800 microspheres 50 microns in diameter via the left internal carotid artery under 2% halothane anesthesia. Daily oral administration of nefiracetam (30 mg/kg/d) was started 9 days after embolization. Nefiracetam caused significant (p < 0.05) improvement of deficits in the learning of both water maze and passive avoidance tasks beginning 22 days after embolization of the rats. The drug also significantly restored decreases in cortical choline acetyltransferase (p < 0.05) and hippocampal glutamic acid decarboxylase activities (p < 0.01) in the embolized cerebral hemisphere and significantly increased cortical choline acetyltransferase (p < 0.05) and acetylcholinesterase activities (p < 0.05) in the contralateral cerebral hemisphere 21 days after embolization. These results demonstrate that nefiracetam improves cognitive dysfunction in the late phase in embolized rats and suggest that the effect is at least partly due to the increase in glutamic acid decarboxylase, choline acetyltranseferase and acetylcholinesterase activities.

摘要

研究了奈非西坦(DM - 9384,化学物质登记号77191 - 36 - 7)对实验性脑栓塞大鼠学习行为以及胆碱能和γ-氨基丁酸能神经递质系统的影响。在2%氟烷麻醉下,通过左颈内动脉向雄性Wistar大鼠注射800个直径50微米的微球,诱导形成脑栓塞。栓塞9天后开始每日口服奈非西坦(30毫克/千克/天)。从大鼠栓塞22天后开始,奈非西坦显著(p < 0.05)改善了水迷宫和被动回避任务学习中的缺陷。该药物还显著恢复了栓塞脑半球皮质胆碱乙酰转移酶活性的降低(p < 0.05)以及海马谷氨酸脱羧酶活性的降低(p < 0.01),并在栓塞21天后显著增加了对侧脑半球皮质胆碱乙酰转移酶活性(p < 0.05)和乙酰胆碱酯酶活性(p < 0.05)。这些结果表明,奈非西坦改善了栓塞大鼠后期的认知功能障碍,并提示该作用至少部分归因于谷氨酸脱羧酶、胆碱乙酰转移酶和乙酰胆碱酯酶活性的增加。

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