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氧化应激在胎儿编程中的影响。

Impact of oxidative stress in fetal programming.

作者信息

Thompson Loren P, Al-Hasan Yazan

机构信息

Department of Obstetrics, Gynecology and Reproductive Sciences, University of Maryland School of Medicine, 11-029 Bressler Research Building, 655 W. Baltimore Street, Baltimore, MD 21201, USA.

出版信息

J Pregnancy. 2012;2012:582748. doi: 10.1155/2012/582748. Epub 2012 Jul 11.

DOI:10.1155/2012/582748
PMID:22848830
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3403156/
Abstract

Intrauterine stress induces increased risk of adult disease through fetal programming mechanisms. Oxidative stress can be generated by several conditions, such as, prenatal hypoxia, maternal under- and overnutrition, and excessive glucocorticoid exposure. The role of oxidant molecules as signaling factors in fetal programming via epigenetic mechanisms is discussed. By linking oxidative stress with dysregulation of specific target genes, we may be able to develop therapeutic strategies that protect against organ dysfunction in the programmed offspring.

摘要

宫内应激通过胎儿编程机制增加成年疾病的风险。氧化应激可由多种情况产生,如产前缺氧、母体营养不足和营养过剩以及糖皮质激素暴露过多。本文讨论了氧化分子作为信号因子通过表观遗传机制在胎儿编程中的作用。通过将氧化应激与特定靶基因的失调联系起来,我们或许能够制定出针对程序化后代器官功能障碍的治疗策略。

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本文引用的文献

1
Fetal stress and programming of hypoxic/ischemic-sensitive phenotype in the neonatal brain: mechanisms and possible interventions.胎儿应激与新生儿脑缺氧/缺血敏感表型的编程:机制与可能的干预措施。
Prog Neurobiol. 2012 Aug;98(2):145-65. doi: 10.1016/j.pneurobio.2012.05.010. Epub 2012 May 22.
2
Protective effect of N-acetylcysteine on liver damage during chronic intrauterine hypoxia in fetal guinea pig.N-乙酰半胱氨酸对胎鼠慢性宫内缺氧致肝损伤的保护作用。
Reprod Sci. 2012 Sep;19(9):1001-9. doi: 10.1177/1933719112440052. Epub 2012 Apr 24.
3
Developmental programming of cardiovascular dysfunction by prenatal hypoxia and oxidative stress.产前低氧和氧化应激对心血管功能障碍的发育编程作用。
PLoS One. 2012;7(2):e31017. doi: 10.1371/journal.pone.0031017. Epub 2012 Feb 13.
4
A role for xanthine oxidase in the control of fetal cardiovascular function in late gestation sheep.黄嘌呤氧化酶在妊娠晚期绵羊胎儿心血管功能控制中的作用。
J Physiol. 2012 Apr 15;590(8):1825-37. doi: 10.1113/jphysiol.2011.224576. Epub 2012 Feb 13.
5
Ascorbate prevents placental oxidative stress and enhances birth weight in hypoxic pregnancy in rats.抗坏血酸可预防缺氧妊娠大鼠胎盘氧化应激并增加出生体重。
J Physiol. 2012 Mar 15;590(6):1377-87. doi: 10.1113/jphysiol.2011.226340. Epub 2012 Jan 30.
6
Chronic hypoxia increases peroxynitrite, MMP9 expression, and collagen accumulation in fetal guinea pig hearts.慢性缺氧增加胎鼠心脏过氧亚硝酸盐、MMP9 表达和胶原积聚。
Pediatr Res. 2012 Jan;71(1):25-31. doi: 10.1038/pr.2011.10.
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Hypoxia-derived oxidative stress mediates epigenetic repression of PKCε gene in foetal rat hearts.低氧诱导的氧化应激介导 PKCe 基因在胎鼠心脏中的表观遗传抑制。
Cardiovasc Res. 2012 Feb 1;93(2):302-10. doi: 10.1093/cvr/cvr322. Epub 2011 Dec 2.
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Metabolic programming, epigenetics, and gestational diabetes mellitus.代谢编程、表观遗传学与妊娠期糖尿病。
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