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怀孕小鼠的高膳食叶酸水平会导致假性亚甲基四氢叶酸还原酶(MTHFR)缺乏和甲基代谢改变,使后代出现胚胎生长延迟和短期记忆受损的情况。

High dietary folate in pregnant mice leads to pseudo-MTHFR deficiency and altered methyl metabolism, with embryonic growth delay and short-term memory impairment in offspring.

作者信息

Bahous Renata H, Jadavji Nafisa M, Deng Liyuan, Cosín-Tomás Marta, Lu Jessica, Malysheva Olga, Leung Kit-Yi, Ho Ming-Kai, Pallàs Mercè, Kaliman Perla, Greene Nicholas D E, Bedell Barry J, Caudill Marie A, Rozen Rima

机构信息

Departments of Human Genetics and Pediatrics, Research Institute of the McGill University Health Center, Montreal, Quebec, Canada.

Department of Neuroscience, Carleton University, Ottawa, Ontario, Canada.

出版信息

Hum Mol Genet. 2017 Mar 1;26(5):888-900. doi: 10.1093/hmg/ddx004.

Abstract

Methylenetetrahydrofolate reductase (MTHFR) generates methyltetrahydrofolate for methylation reactions. Severe MTHFR deficiency results in homocystinuria and neurologic impairment. Mild MTHFR deficiency (677C > T polymorphism) increases risk for complex traits, including neuropsychiatric disorders. Although low dietary folate impacts brain development, recent concerns have focused on high folate intake following food fortification and increased vitamin use. Our goal was to determine whether high dietary folate during pregnancy affects brain development in murine offspring. Female mice were placed on control diet (CD) or folic acid-supplemented diet (FASD) throughout mating, pregnancy and lactation. Three-week-old male pups were evaluated for motor and cognitive function. Tissues from E17.5 embryos, pups and dams were collected for choline/methyl metabolite measurements, immunoblotting or gene expression of relevant enzymes. Brains were examined for morphology of hippocampus and cortex. Pups of FASD mothers displayed short-term memory impairment, decreased hippocampal size and decreased thickness of the dentate gyrus. MTHFR protein levels were reduced in FASD pup livers, with lower concentrations of phosphocholine and glycerophosphocholine in liver and hippocampus, respectively. FASD pup brains showed evidence of altered acetylcholine availability and Dnmt3a mRNA was reduced in cortex and hippocampus. E17.5 embryos and placentas from FASD dams were smaller. MTHFR protein and mRNA were reduced in embryonic liver, with lower concentrations of choline, betaine and phosphocholine. Embryonic brain displayed altered development of cortical layers. In summary, high folate intake during pregnancy leads to pseudo-MTHFR deficiency, disturbed choline/methyl metabolism, embryonic growth delay and memory impairment in offspring. These findings highlight the unintended negative consequences of supplemental folic acid.

摘要

亚甲基四氢叶酸还原酶(MTHFR)产生甲基四氢叶酸用于甲基化反应。严重的MTHFR缺乏会导致同型胱氨酸尿症和神经功能障碍。轻度MTHFR缺乏(677C>T多态性)会增加包括神经精神疾病在内的复杂性状的风险。尽管低膳食叶酸会影响大脑发育,但近期的关注点集中在食品强化和维生素使用增加后叶酸摄入量过高的问题上。我们的目标是确定孕期高膳食叶酸是否会影响小鼠后代的大脑发育。在整个交配、怀孕和哺乳期,将雌性小鼠置于对照饮食(CD)或补充叶酸的饮食(FASD)中。对三周龄的雄性幼崽进行运动和认知功能评估。收集E17.5胚胎、幼崽和母鼠的组织,用于胆碱/甲基代谢物测量、免疫印迹或相关酶的基因表达分析。检查大脑中海马体和皮质的形态。FASD母鼠的幼崽表现出短期记忆受损、海马体尺寸减小和齿状回厚度降低。FASD幼崽肝脏中的MTHFR蛋白水平降低,肝脏和海马体中磷酸胆碱和甘油磷酸胆碱的浓度分别降低。FASD幼崽大脑显示出乙酰胆碱可用性改变的证据,皮质和海马体中的Dnmt3a mRNA减少。FASD母鼠的E17.5胚胎和胎盘较小。胚胎肝脏中的MTHFR蛋白和mRNA减少,胆碱、甜菜碱和磷酸胆碱的浓度降低。胚胎大脑显示出皮质层发育改变。总之,孕期高叶酸摄入会导致假性MTHFR缺乏、胆碱/甲基代谢紊乱、胚胎生长延迟和后代记忆受损。这些发现突出了补充叶酸意想不到的负面后果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44c/5409086/ab79050c01d0/ddx004f1.jpg

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