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肠道和肝脏如何休眠。

How the gut and liver hibernate.

机构信息

Department of Biology, University of Wisconsin-Oshkosh, Oshkosh, WI, United States of America.

Department of Molecular Biology, Cell Biology and Biochemistry, Brown University, Providence, RI, United States of America.

出版信息

Comp Biochem Physiol A Mol Integr Physiol. 2021 Mar;253:110875. doi: 10.1016/j.cbpa.2020.110875. Epub 2020 Dec 25.

Abstract

For hibernating mammals, the transition from summer active to winter hibernation seasons come with significant remodeling at cellular, organ and whole organism levels. This review summarizes and synthesizes what is known about hibernation-related remodeling in the gastrointestinal tract of the thirteen-lined ground squirrel, including intestinal and hepatic physiology and the gut microbiota. Hibernation alters intestinal epithelial, immune and cell survival pathways in ways that point to a protective phenotype in the face of prolonged fasting and major fluctuations in nutrient and oxygen delivery during torpor-arousal cycles. The prolonged fasting associated with hibernation alters lipid metabolism and systemic cholesterol dynamics, with both the gut and liver participating in these changes. Fasting also affects the gut microbiota, altering the abundance, composition and diversity of gut microbes and impacting the metabolites they produce in ways that may influence hibernation-related traits in the host. Finally, interventional studies have demonstrated that the hibernation phenotype confers resistance to experimental ischemia-reperfusion injury in both gut and liver, suggesting potential therapeutic roadmaps. We propose that the plasticity inherent to hibernation biology may contribute to this stress tolerance, and in the spirit of August Krogh, makes hibernators particularly valuable for study to identify solutions to certain problems.

摘要

对于冬眠哺乳动物来说,从夏季活跃到冬季冬眠季节的转变伴随着细胞、器官和整个生物体水平的显著重塑。本综述总结和综合了关于十三线地松鼠胃肠道中与冬眠相关的重塑的已知知识,包括肠道和肝脏生理学以及肠道微生物群。冬眠以延长禁食和在休眠-觉醒循环期间营养和氧气输送的剧烈波动为特征,改变了肠道上皮、免疫和细胞存活途径,指向了一种保护表型。与冬眠相关的长时间禁食改变了脂质代谢和系统胆固醇动力学,肠道和肝脏都参与了这些变化。禁食还会影响肠道微生物群,改变肠道微生物的丰度、组成和多样性,并以可能影响宿主与冬眠相关特征的方式影响它们产生的代谢物。最后,干预性研究表明,冬眠表型赋予了肠道和肝脏对实验性缺血再灌注损伤的抗性,这表明可能存在治疗方案。我们提出,冬眠生物学固有的可塑性可能有助于这种应激耐受,并且本着奥古斯特·克罗格(August Krogh)的精神,使冬眠动物特别有价值,可以研究确定某些问题的解决方案。

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