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2-苯乙炔基-正丁基碲减轻了小鼠淀粉样β肽(25-35)诱导的学习和记忆损伤。

2-Phenylethynyl-butyltellurium attenuates amyloid-β peptide(25-35)-induced learning and memory impairments in mice.

机构信息

Departamento de Química, Centro de Ciências Naturais e Exatas, Universidade Federal de Santa Maria, Santa Maria, Brasil.

出版信息

J Neurosci Res. 2013 Jun;91(6):848-53. doi: 10.1002/jnr.23211. Epub 2013 Mar 29.

Abstract

Our previous study demonstrated that 2-phenylethynyl-butyltellurium (PEBT), an organotellurium compound, enhances memory in mice. In this study, the effects of PEBT on cognitive impairment induced by Aβ25-35 were assessed by Morris water maze and step-down inhibitory avoidance tasks. Mice received a single intracerebroventricular injection of Aβ25-35 (3 nmol/3 μl/per site) and a daily oral administration of PEBT (1 mg/kg, for 10 days). PEBT significantly improved Aβ-induced learning deficits on the training session in the Morris water maze. At the probe trial session, PEBT significantly decreased the escape latency and increased the number of crossings in the platform local compared with the Aβ-treated group. PEBT significantly improved Aβ-induced memory impairment in the step-down inhibitory avoidance task. General locomotor activity was similar in all groups. This study showed that PEBT ameliorated the impairments of spatial and nonspatial long-term memory evaluated on Morris water maze and step-down inhibitory avoidance tasks, respectively. The results suggest that PEBT could be considered a candidate for the prevention of memory deficits such as those observed in Alzheimer's disease.

摘要

我们之前的研究表明,2-苯乙炔基丁基碲(PEBT),一种有机碲化合物,可增强小鼠的记忆力。在这项研究中,通过 Morris 水迷宫和下台阶抑制回避任务评估了 PEBT 对 Aβ25-35 诱导的认知障碍的影响。小鼠接受单次侧脑室注射 Aβ25-35(3 nmol/3 μl/部位)和每日口服 PEBT(1 mg/kg,连续 10 天)。PEBT 显著改善了 Morris 水迷宫训练阶段中 Aβ引起的学习缺陷。在探测试验阶段,与 Aβ 处理组相比,PEBT 显著降低了逃避潜伏期并增加了平台局部的穿越次数。PEBT 显著改善了 Aβ 诱导的下台阶抑制回避任务中的记忆障碍。各组的一般运动活性相似。这项研究表明,PEBT 可改善 Morris 水迷宫和下台阶抑制回避任务评估的空间和非空间长期记忆损伤。结果表明,PEBT 可被视为预防阿尔茨海默病中观察到的记忆缺陷的候选药物。

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