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甲苯抑制成年小鼠海马神经发生。

Toluene inhibits hippocampal neurogenesis in adult mice.

机构信息

Department of Veterinary Anatomy, College of Veterinary Medicine and Animal Medical Institute, Chonnam National University, Gwangju 500-757, South Korea.

出版信息

Pharmacol Biochem Behav. 2010 Feb;94(4):588-94. doi: 10.1016/j.pbb.2009.11.015. Epub 2009 Dec 5.

Abstract

Toluene, a representative industrial solvent and abused inhalant, decreases neuronal activity in vitro and causes mental depression and cognitive impairment in humans. However, the effects of toluene on brain function and the sites of its action are poorly understood. This study investigated the temporal changes of neurogenesis in the hippocampus of adult C57BL/6 mice after acute administration of toluene using two immunohistochemical markers for neurogenesis, Ki-67 and doublecortin (DCX). In addition, after toluene treatment, depression-like behaviors and learning and memory tasks were examined to assess hippocampal neurogenesis-related behavioral dysfunction. The number of Ki-67- and DCX-positive cells in the dentate gyrus of adult hippocampi declined acutely between 0 h and 24 h after toluene treatment (500 mg/kg, i.p.) and increased gradually from 2 to 8 days post-administration. The level of Ki-67 and DCX immunoreactivity decreased in a dose-dependent manner within the range of toluene administered (0-1000 mg/kg). In tail suspension and forced-swim tests performed at 1 and 4 days after toluene treatment (500 mg/kg), mice showed significant depression-like behaviors compared to the vehicle-treated controls. In the contextual fear conditioning and object recognition memory test, the mice trained at 1 and 4 days after toluene treatment showed significant memory defects compared to the vehicle-treated controls. This study suggests that acute exposure to toluene reduces the rate of adult hippocampal neurogenesis and can cause hippocampal dysfunction such as depression and cognitive impairment.

摘要

甲苯,一种有代表性的工业溶剂和被滥用的吸入剂,会降低体外神经元的活性,并导致人类精神抑郁和认知障碍。然而,甲苯对大脑功能的影响及其作用部位仍知之甚少。本研究使用两种神经发生的免疫组织化学标志物,Ki-67 和双皮质素(DCX),研究了成年 C57BL/6 小鼠急性给予甲苯后海马体神经发生的时间变化。此外,在甲苯处理后,通过抑郁样行为和学习记忆任务来评估与海马体神经发生相关的行为功能障碍。甲苯处理(500mg/kg,ip)后 0 小时至 24 小时内,成年海马齿状回中 Ki-67 和 DCX 阳性细胞的数量急剧减少,并且在给药后 2 至 8 天逐渐增加。Ki-67 和 DCX 免疫反应性的水平在甲苯给药范围内(0-1000mg/kg)呈剂量依赖性降低。在甲苯处理(500mg/kg)后 1 天和 4 天进行的悬尾和强迫游泳测试中,与载体处理的对照组相比,小鼠表现出明显的抑郁样行为。在情境恐惧条件反射和物体识别记忆测试中,与载体处理的对照组相比,在甲苯处理后 1 天和 4 天接受训练的小鼠表现出明显的记忆缺陷。本研究表明,急性暴露于甲苯会降低成年海马体神经发生的速度,并可能导致海马体功能障碍,如抑郁和认知障碍。

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