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缺血后给予[纠正给药]而非缺血前给予[纠正给药]NG-硝基-L-精氨酸,可通过抑制反复脑缺血后海马中NOx-的延迟增加来预防空间记忆障碍和细胞凋亡。

Post-ischemic administration [correction of administeration] but not pre-ischemic administration [correction of administeration] of NG-nitro-L-arginine prevents spatial memory impairments and apoptosis by an inhibition of a delayed increase in NOx- in the hippocampus following repeated cerebral ischemia.

作者信息

Mishima K, Pu F, Kaneko T, Egashira N, Iwasaki K, Fujiwara M

机构信息

Department of Neuropharmacology, Faculty of Pharmaceutical Sciences, Fukuoka University, Fukuoka 814-0180, Japan.

出版信息

Neuropharmacology. 2003 Mar;44(4):533-40. doi: 10.1016/s0028-3908(02)00404-5.

DOI:10.1016/s0028-3908(02)00404-5
PMID:12646290
Abstract

In the present study, we investigated the effects of N(G)-nitro-L-arginine (L-NAME), an inhibitor of nitric oxide synthase, on repeated cerebral ischemia-induced impairment of spatial memory of the 8-arm radial maze in rats. Repeated ischemia (10 min ischemia x 2 times with 1 h interval) impaired the spatial memory in the 8-arm radial maze test and produced apoptosis in the hippocampus 7 days after final occlusion, and gradually increased the NO(x)(-) levels approximately 30-180 min after the second reperfusion. Post-ischemic administration of L-NAME at a dose of 50 mg/kg, i.p. 30 min following the second occlusion, significantly attenuated the repeated ischemia-induced impairment of spatial memory in the 8-arm radial maze test and suppressed apoptosis in the hippocampus, and also significantly suppressed a delayed increase in the NO(x)(-) levels induced by repeated ischemia. However, pre-ischemic administration of L-NAME at a dose of 50 mg/kg, i.p. 30 min before the first occlusion, caused about 90% mortality (the mortality rate of vehicle-treated group was 10%). These results suggest that the delayed generation of NO(x)(-) may cause spatial memory impairment and induction of apoptosis in the hippocampus in rats subjected to repeated ischemia.

摘要

在本研究中,我们研究了一氧化氮合酶抑制剂N(G)-硝基-L-精氨酸(L-NAME)对大鼠反复脑缺血诱导的八臂放射状迷宫空间记忆损伤的影响。反复缺血(10分钟缺血×2次,间隔1小时)损害了八臂放射状迷宫试验中的空间记忆,并在最后一次闭塞后7天在海马体中产生细胞凋亡,且在第二次再灌注后约30 - 180分钟逐渐增加NO(x)(-)水平。在第二次闭塞后30分钟腹腔注射50mg/kg剂量的L-NAME进行缺血后给药,显著减轻了反复缺血诱导的八臂放射状迷宫试验中的空间记忆损伤,并抑制了海马体中的细胞凋亡,还显著抑制了反复缺血诱导的NO(x)(-)水平的延迟升高。然而,在第一次闭塞前30分钟腹腔注射50mg/kg剂量的L-NAME进行缺血前给药,导致约90%的死亡率(溶剂处理组的死亡率为10%)。这些结果表明,NO(x)(-)的延迟产生可能导致反复缺血大鼠海马体中的空间记忆损伤和细胞凋亡诱导。

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