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母体叶酸缺乏通过与大鼠胎儿脑中Bcl-2相关的miR-34a刺激神经细胞凋亡。

Maternal folic acid deficiency stimulates neural cell apoptosis via miR-34a associated with Bcl-2 in the rat foetal brain.

作者信息

Li Wen, Li Zhenshu, Zhou Dezheng, Zhang Xumei, Yan Jing, Huang Guowei

机构信息

Department of Nutrition and Food Science, School of Public Health, Tianjin Medical University, Tianjin, 300070, China.

Department of Social Medicine and Health Administration, School of Public Health, Tianjin Medical University, Tianjin, 300070, China.

出版信息

Int J Dev Neurosci. 2019 Feb;72:6-12. doi: 10.1016/j.ijdevneu.2018.11.002. Epub 2018 Nov 14.

Abstract

Embryonic development is a critical period wherein brain neurons are generated and organized. Maternal dietary folate, a cofactor in one-carbon metabolism, modulates neurogenesis and apoptosis in foetal brain neurons. We hypothesized that aberrant neuronal apoptosis may affect the development of the central nervous system during maternal folic acid deficiency, with evident effects because maternal folic acid deficiency modulates the microRNA-34a associated with Bcl-2 pathway during embryonic development. Four-week-old female Sprague-Dawley rats were divided randomly into two groups (10 rats per group): a folate-deficient diet group and a folate-normal diet group. The diets were administered to the rats 60 d before mating, which was continued for the pregnant dams until parturition. Maternal folic acid deficiency increased neuronal apoptosis in the hippocampus and the cortex in the offspring. Furthermore, maternal folic acid deficiency increased the ratio of cleaved caspase-3/caspase-3, followed by an increase in caspase-3 activity. Moreover, maternal folic acid deficiency downregulated Bcl-2 and upregulated Bax, and this effect associate with maternal folic acid deficient increases expression of microRNA-34a. Together, the present results indicate that maternal folic acid deficiency stimulates neuronal apoptosis via microRNA-34a associated with Bcl-2 signalling in rat offspring.

摘要

胚胎发育是一个关键时期,在此期间脑神经元生成并组织起来。母体饮食中的叶酸作为一碳代谢的辅助因子,可调节胎儿脑神经元的神经发生和凋亡。我们推测,母体叶酸缺乏期间异常的神经元凋亡可能会影响中枢神经系统的发育,由于母体叶酸缺乏在胚胎发育过程中调节与Bcl-2通路相关的微小RNA-34a,故影响明显。将四周龄的雌性Sprague-Dawley大鼠随机分为两组(每组10只):叶酸缺乏饮食组和叶酸正常饮食组。在交配前60天给大鼠喂食这些饮食,并持续给怀孕的母鼠喂食直至分娩。母体叶酸缺乏会增加后代海马体和皮质中的神经元凋亡。此外,母体叶酸缺乏会增加裂解的半胱天冬酶-3/半胱天冬酶-3的比例,随后半胱天冬酶-3活性增加。此外,母体叶酸缺乏会下调Bcl-2并上调Bax,并且这种效应与母体叶酸缺乏会增加微小RNA-34a的表达有关。总之,目前的结果表明,母体叶酸缺乏通过与大鼠后代Bcl-2信号相关的微小RNA-34a刺激神经元凋亡。

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