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Prenatal Stress in Maternal Hyperhomocysteinemia: Impairments in the Fetal Nervous System Development and Placental Function

机译:孕产妇高表症的产前压力:胎儿神经系统开发和胎盘功能的损伤

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The article presents current views on maternal hyperhomocysteinemia (HHcy) as an important factor causing prenatal stress and impaired nervous system development in fetuses and newborns in early ontogenesis, as well as complications in adulthood. Experimental data demonstrate that prenatal HHcy (PHHcy) affects the morphological maturation of the brain and activity of its neurotransmitter systems. Cognitive deficit observed in the offspring subjected to PHHcy in experimental studies can presumably cause the predisposition to various neurodegenerative diseases, as the role of maternal HHcy in the pathogenesis such diseases has been proven in clinical studies. The review also discusses molecular mechanisms of the HHcy neurotoxic action on the nervous system development in the prenatal and early postnatal periods, which include oxidative stress, apoptosis activation, changes in the DNA methylation patterns and microRNA levels, altered expression and processing of neurotrophins, and neuroinflammation induced by an increased production of pro-inflammatory cytokines. Special attention is given to the maternal HHcy impact on the placenta function and its possible contribution to the brain function impairments in the offspring. Published data suggest that some effects of PHHcy on the developing fetal brain can be due to the disturbances in the transport functions of the placenta resulting in an insufficient supply of nutrients necessary for the proper formation and functioning of brain structures.
机译:本文对母体高胞嘧啶血症(HHCy)的目前看法是引起产前应激和胎儿发育中的神经系统发育受损的重要因素,以及早期形成的新生儿,以及成年的并发症。实验数据表明产前HHCY(PHHCY)影响其神经递质系统的大脑和活性的形态学成熟。在实验研究中经受PhHcy的后代观察到的认知缺陷可能可能会导致各种神经变性疾病的易感性,因为母体HHCY在发病机制中的作用已被证明在临床研究中已被证明。审查还讨论了产前和早期后期神经系统发育的Hhcy神经毒性作用的分子机制,包括氧化应激,凋亡激活,DNA甲基化模式的变化和MicroRNA水平,神经营养蛋白的表达和加工改变通过增加促炎细胞因子的产生诱导的神经炎炎症。特别注意母体HHCY对胎盘作用的影响及其对后代脑功能损伤的可能贡献。已发表的数据表明,Phhcy对发育胎儿大脑的一些影响可能是由于胎盘的运输功能中的紊乱导致脑结构正确形成和运作所需的营养素供应不足。

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