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MK-801可预防大鼠硫胺素诱导性脑病所产生的脑损伤和延迟性非匹配样本缺陷。

MK-801 prevents brain lesions and delayed-nonmatching-to-sample deficits produced by pyrithiamine-induced encephalopathy in rats.

作者信息

Robinson J K, Mair R G

机构信息

University of New Hampshire, Durham 03824.

出版信息

Behav Neurosci. 1992 Aug;106(4):623-33.

PMID:1386989
Abstract

Rats were trained on a spatial delayed-nonmatching-to-sample (DNMTS) task and assigned by block randomization to one of four treatments: pyrithiamine-induced thiamine deficiency (PTD), PTD with administration of MK-801 after 12 days, control with MK-801 treatment, and control without MK-801. After 15 days of treatment followed by 21 days of recovery, the PTD rats showed significant deficits for DNMTS accuracy at retention intervals (RI) that ranged from 3.0 s to 15.0 s, the RIs that produced 75% accuracy on DNMTS in staircase training, and the rate at which a novel radial arm maze task was learned. The PTD-treated rats had consistent lesions in the thalamus and the mammillary bodies. MK-801 protected rats from both behavioral deficits and brain lesions (assessed quantitatively and qualitatively) that were produced by the PTD treatment.

摘要

大鼠接受空间延迟非匹配样本(DNMTS)任务训练,并通过区组随机化分配到四种处理之一:硫胺素缺乏诱导的硫胺素缺乏(PTD)、12天后给予MK-801的PTD、MK-801处理的对照组和未给予MK-801的对照组。在15天的治疗后接着21天的恢复,PTD大鼠在3.0秒至15.0秒的保持间隔(RI)(阶梯训练中产生75%DNMTS准确率的RI)以及新的放射状臂迷宫任务的学习速率方面,表现出显著的DNMTS准确性缺陷。接受PTD处理的大鼠在丘脑和乳头体有一致性损伤。MK-801保护大鼠免受PTD处理所产生的行为缺陷和脑损伤(进行定量和定性评估)。

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MK-801 prevents brain lesions and delayed-nonmatching-to-sample deficits produced by pyrithiamine-induced encephalopathy in rats.MK-801可预防大鼠硫胺素诱导性脑病所产生的脑损伤和延迟性非匹配样本缺陷。
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