The roles of the gut microbiota, metabolites, and epigenetics in the effects of maternal exercise on offspring metabolism.

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Jing Ren, Liyuan Zhou, Shunhua Li, Qian Zhang, Xinhua Xiao
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引用次数: 0

Abstract

Metabolic diseases, including obesity, dyslipidemia, and type 2 diabetes, have become severe challenges worldwide. The developmental origins of health and disease (DOHaD) hypothesis suggests that an adverse intrauterine environment can increase the risk of metabolic disorders in offspring. Studies have demonstrated that maternal exercise is an effective intervention for improving the offspring metabolic health. However, the pathways through which exercise works are unclear. It has been reported that the gut microbiota mediates the effect of maternal exercise on offspring metabolism, and epigenetic modifications have also been proposed to be important molecular mechanisms. Microbial metabolites can influence epigenetics by providing substrates for DNA or histone modifications, binding to G-protein coupled receptors to affect downstream pathways, or regulating the activity of epigenetic modifying enzymes. This review aims to summarize the intergenerational effect of maternal exercise and proposes that gut microbiota-metabolites-epigenetic regulation is an important mechanism by which maternal exercise improves offspring metabolism, which may yield novel targets for the early prevention and intervention of metabolic diseases.

肠道微生物群、代谢物和表观遗传学在母体运动对后代代谢影响中的作用。
肥胖、血脂异常和 2 型糖尿病等代谢性疾病已成为全球面临的严峻挑战。健康与疾病的发育起源(DOHaD)假说认为,不利的宫内环境会增加后代患代谢性疾病的风险。研究表明,母体运动是改善后代代谢健康的有效干预措施。然而,运动发挥作用的途径尚不清楚。据报道,肠道微生物群介导了母体运动对后代代谢的影响,表观遗传修饰也被认为是重要的分子机制。微生物代谢物可通过为 DNA 或组蛋白修饰提供底物、与 G 蛋白偶联受体结合以影响下游途径或调节表观遗传修饰酶的活性来影响表观遗传学。本综述旨在总结母体运动的代际效应,并提出肠道微生物群-代谢物-表观遗传调控是母体运动改善后代代谢的重要机制,这可能为早期预防和干预代谢性疾病提供新的靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.80
自引率
0.00%
发文量
98
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Endocrinology and Metabolism publishes original, mechanistic studies on the physiology of endocrine and metabolic systems. Physiological, cellular, and molecular studies in whole animals or humans will be considered. Specific themes include, but are not limited to, mechanisms of hormone and growth factor action; hormonal and nutritional regulation of metabolism, inflammation, microbiome and energy balance; integrative organ cross talk; paracrine and autocrine control of endocrine cells; function and activation of hormone receptors; endocrine or metabolic control of channels, transporters, and membrane function; temporal analysis of hormone secretion and metabolism; and mathematical/kinetic modeling of metabolism. Novel molecular, immunological, or biophysical studies of hormone action are also welcome.
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