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假马齿苋改善N(ω)-硝基-L-精氨酸诱导而非MK-801诱导的记忆缺失:一项小鼠莫里斯水迷宫研究

Bacopa monniera alleviates N(omega)-nitro-L-arginine arginine-induced but not MK-801-induced amnesia: a mouse Morris watermaze study.

作者信息

Saraf M K, Prabhakar S, Anand A

机构信息

Neuroscience Research Laboratory, Department of Neurology, Post Graduate Institute of Medical Education and Research, Sector 12, Chandigarh 160012, India.

出版信息

Neuroscience. 2009 Apr 21;160(1):149-55. doi: 10.1016/j.neuroscience.2009.02.005.

Abstract

N-methyl-D-aspartate (NMDA) receptor and nitricoxide syntheses are the emerging target sites for development of novel drug molecules because their modulation affects the long term potentiation (LTP) process. NMDA receptor antagonists and nitric oxide synthase inhibitors induce amnesia in animals and therefore have been employed for evaluation of efficacy of several novel antiamnesic agents.Bacopa monniera Linn (syn. Brahmi) is commonly used in the ancient Indian medical system for improvement of memory deficit.We have earlier described the involvement of GABAergic and cholinergic system to account for the antiamnesic effects of B. monniera on diazepam- and scopolamine-induced amnesia.In extension to our previous study this study was designed to investigate the downstream mechanism of B. monniera by evaluation of its effect on MK-801 (an NMDA receptor antagonist) and N(w)-nitro-L-arginine (L-NNA) (a nitric oxide inhibitor)induced memory deficit. We used a Morris water maze scale and compared the degree of reversal of amnesia induced by the two agents. Male Swiss albino mice were subjected to a Rotarod muscle incoordination test followed by water maze tasks.Our data revealed that L-NNA and MK-801 produced anterograde and retrograde amnesia and B. monniera significantly attenuated the L-NNA-induced anterograde amnesia, partially reversing L-NNA-induced retrograde amnesia. On the other hand, B. monniera neither attenuated the MK-801-induced anterograde amnesia nor improved retrograde amnesia caused by it.

摘要

N-甲基-D-天冬氨酸(NMDA)受体和一氧化氮合成是新型药物分子开发中新兴的靶点,因为对它们的调节会影响长时程增强(LTP)过程。NMDA受体拮抗剂和一氧化氮合酶抑制剂可诱导动物失忆,因此已被用于评估几种新型抗失忆药物的疗效。假马齿苋(学名:Bacopa monniera Linn,同义词:Brahmi)在古印度医学体系中常用于改善记忆缺陷。我们之前已经描述过,GABA能和胆碱能系统参与了假马齿苋对安定和东莨菪碱诱导失忆的抗失忆作用。作为我们之前研究的延伸,本研究旨在通过评估假马齿苋对MK-801(一种NMDA受体拮抗剂)和N(ω)-硝基-L-精氨酸(L-NNA)(一种一氧化氮抑制剂)诱导的记忆缺陷的影响,来研究其下游机制。我们使用了莫里斯水迷宫实验,并比较了这两种药物诱导失忆的逆转程度。对雄性瑞士白化小鼠进行转棒不协调试验,然后进行水迷宫任务。我们的数据显示,L-NNA和MK-801产生了顺行性和逆行性失忆,而假马齿苋显著减轻了L-NNA诱导的顺行性失忆,部分逆转了L-NNA诱导的逆行性失忆。另一方面,假马齿苋既没有减轻MK-801诱导的顺行性失忆,也没有改善由其引起的逆行性失忆。

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