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断奶后叶酸缺乏通过齿状回神经元不成熟诱导小鼠抑郁状态。

Post-weaning folate deficiency induces a depression-like state via neuronal immaturity of the dentate gyrus in mice.

机构信息

Laboratory of Functional Biomolecules and Chemical Pharmacology, Faculty of Pharmaceutical Sciences, Setsunan University, 45-1 Nagaotoge-cho, Hirakata, Osaka 573-0101, Japan.

Laboratory of Functional Biomolecules and Chemical Pharmacology, Faculty of Pharmaceutical Sciences, Setsunan University, 45-1 Nagaotoge-cho, Hirakata, Osaka 573-0101, Japan.

出版信息

J Pharmacol Sci. 2020 Jun;143(2):97-105. doi: 10.1016/j.jphs.2020.02.007. Epub 2020 Feb 29.

DOI:10.1016/j.jphs.2020.02.007
PMID:32173264
Abstract

Folate deficiency has been suggested as a risk factor for depression in preclinical and clinical studies. Several hypotheses of mechanisms underlying folate deficiency-induced depressive symptoms have been proposed, but the detailed mechanisms are still unclear. In this study, we assessed whether post-weaning folate deficiency affect neurological and psychological function. The low folate diet-fed mice showed depression-like behavior in the forced swim test. In contrast, spontaneous locomotor activity, social behavior, coordinated motor skills, anxiety-like behavior and spatial memory did not differ between control and low folate diet-fed mice. In the dentate gyrus (DG) of the hippocampus, decreased number of newborn mature neurons and increased number of immature neurons were observed in low folate diet-fed mice. Staining with Golgi-Cox method revealed that dendritic complexity, spine density and the number of mature spines of neurons were markedly reduced in the DG of low folate diet-fed mice. Stress response of neurons indicated as c-Fos expression was also reduced in the DG of low folate diet-fed mice. These results suggest that reduction in the degree of maturation of newborn hippocampal neurons underlies folate deficiency-induced depressive symptoms.

摘要

叶酸缺乏症已在临床前和临床研究中被认为是抑郁症的一个风险因素。已经提出了几种叶酸缺乏引起抑郁症状的机制假说,但详细的机制仍不清楚。在这项研究中,我们评估了产后叶酸缺乏是否会影响神经和心理功能。低叶酸饮食喂养的小鼠在强迫游泳试验中表现出类似抑郁的行为。相比之下,对照组和低叶酸饮食喂养组的自发运动活动、社交行为、协调运动技能、焦虑样行为和空间记忆没有差异。在海马的齿状回(DG)中,低叶酸饮食喂养的小鼠中观察到新生成熟神经元的数量减少,未成熟神经元的数量增加。高尔基-考克斯染色法显示,低叶酸饮食喂养的小鼠 DG 中的神经元树突复杂性、棘密度和成熟棘的数量明显减少。神经元应激反应的标志 c-Fos 表达也减少了。这些结果表明,新生海马神经元成熟程度的降低是叶酸缺乏引起抑郁症状的基础。

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