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Intestinal epithelial cell NCoR deficiency ameliorates obesity and metabolic syndrome
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作者 Shaocong Hou Hengcai Yu +14 位作者 Caihong Liu Andrew M.F.Johnson Xingfeng Liu Qian Jiang Qijin Zhao Lijuan Kong yanjun wan Xiaowei Xing Yibing Chen Jingwen Chen Qing Wu Peng Zhang Changtao Jiang Bing Cui Pingping Li 《Acta Pharmaceutica Sinica B》 SCIE CAS CSCD 2024年第12期5267-5285,共19页
Nuclear receptor corepressor(NCoR1)interacts with various nuclear receptors and regulates the anabolism and catabolism of lipids.An imbalance in lipid/energy homeostasis is also an important factor in obesity and meta... Nuclear receptor corepressor(NCoR1)interacts with various nuclear receptors and regulates the anabolism and catabolism of lipids.An imbalance in lipid/energy homeostasis is also an important factor in obesity and metabolic syndrome development.In this study,we found that the deletion of NCoR1 in intestinal epithelial cells(IECs)mainly activated the nuclear receptor PPARa and attenuated metabolic syndrome by stimulating thermogenesis.The increase in brown adipose tissue thermogenesis was mediated by gut-derived tricarboxylic acid cycle intermediate succinate,whose production was significantly enhanced by PPARa activation in the fed state.Additionally,NCoR1 deletion derepressed intestinal LXR,increased cholesterol excretion,and impaired duodenal lipid absorption by decreasing bile acid hydrophobicity,thereby reversing the possible negative effects of intestinal PPARa activation.Therefore,the simultaneous regulatory effect of intestinal NCoR1 on both lipid intake and energy expenditure strongly suggests that it is a promising target for developing metabolic syndrome treatment. 展开更多
关键词 Nuclear receptor co-repressor 1 Intestinal epithelium Metabolic syndrome PPAR alpha Liver X receptor THERMOGENESIS SUCCINATE CHOLESTEROL
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