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

机译:2-苯基乙炔基丁基碲减轻小鼠淀粉样蛋白(25-35)诱导的学习和记忆障碍

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摘要

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.
机译:我们之前的研究表明,有机碲化合物2-苯基乙炔基丁基碲(PEBT)可增强小鼠的记忆力。在这项研究中,通过莫里斯水迷宫和逐步抑制性避免任务评估了PEBT对Aβ25-35诱导的认知障碍的影响。小鼠接受单次脑室内注射Aβ25-35(3 nmol / 3μl/每个部位),每天口服PEBT(1 mg / kg,持续10天)。 PEBT在莫里斯水迷宫的训练中显着改善了Aβ诱导的学习缺陷。在探针试验阶段,与Aβ治疗组相比,PEBT显着降低了逃逸潜伏期,并增加了平台局部的穿越次数。 PEBT在降低抑制性避免任务中显着改善了Aβ诱导的记忆障碍。所有组的总体运动活动均相似。这项研究表明,PEBT分别改善了对Morris水迷宫和逐步抑制性避免任务评估的空间和非空间长期记忆的损害。结果表明,PEBT可以被认为是预防记忆缺陷的候选药物,例如在阿尔茨海默氏病中观察到的那些。

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