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禁食和再喂养对小鼠肝脏、脂肪组织和肌肉转录反应的性别差异。

Sex Differences in Liver, Adipose Tissue, and Muscle Transcriptional Response to Fasting and Refeeding in Mice.

机构信息

The Laboratory of Physiological Genetics, The Institute of Cytology and Genetics, 630090 Novosibirsk, Russia.

Department of Physiology, Novosibirsk State University, 630090 Novosibirsk, Russia.

出版信息

Cells. 2019 Nov 27;8(12):1529. doi: 10.3390/cells8121529.

Abstract

Fasting is often used for obesity correction but the "refeeding syndrome" limits its efficiency, and molecular mechanisms underlying metabolic response to different food availability are under investigation. Sex was shown to affect hormonal and metabolic reactions to fasting/refeeding. The aim of this study was to evaluate hormonal and transcriptional responses to fasting and refeeding in male and female C57Bl/6J mice. Sex asymmetry was observed both at the hormonal and transcriptional levels. Fasting (24 h) induced increase in hepatic gene expression, which was associated with elevation of plasma FGF21 and adiponectin levels, and the upregulation of expression of hepatic () and muscle () genes involved in fatty acid oxidation. These changes were more pronounced in females. Refeeding (6 h) evoked hyperinsulinemia and increased hepatic expression of gene related to lipogenesis () only in males and hyperleptinemia and increase in gene expression in muscles and adipose tissues only in females. The results suggest that in mice, one of the molecular mechanisms underlying sex asymmetry in hepatic muscle and expression during fasting is hepatic expression, and the reason for sex asymmetry in hepatic expression during refeeding is male-specific hyperinsulinemia.

摘要

禁食通常用于肥胖症的纠正,但“再喂养综合征”限制了其效率,而不同食物供应下代谢反应的分子机制仍在研究中。性别被证明会影响对禁食/再进食的激素和代谢反应。本研究旨在评估雄性和雌性 C57Bl/6J 小鼠禁食和再进食的激素和转录反应。在激素和转录水平都观察到了性别不对称。禁食(24 小时)诱导肝基因表达增加,这与血浆 FGF21 和脂联素水平升高以及参与脂肪酸氧化的肝()和肌肉()基因的表达上调有关。这些变化在雌性中更为明显。再进食(6 小时)仅在雄性中引起高胰岛素血症和肝基因表达增加,与脂肪生成有关(),而仅在雌性中引起高瘦素血症和肌肉和脂肪组织中基因表达增加。结果表明,在小鼠中,禁食期间肝、肌肉和基因表达的性别不对称的分子机制之一是肝基因表达,而再进食期间肝基因表达的性别不对称的原因是男性特有的高胰岛素血症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc7e/6953068/9afdfd6b89c8/cells-08-01529-g001.jpg

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