Suppr超能文献

生酮饮食抑制线粒体生物发生并诱导心脏纤维化。

Ketogenic diets inhibit mitochondrial biogenesis and induce cardiac fibrosis.

机构信息

Zhongshan Hospital of Fudan University, Obstetrics & Gynecology Hospital of Fudan University, State Key Lab of Genetic Engineering, School of Life Sciences, Key Laboratory of Reproduction Regulation of NPFPC, and Institutes of Biomedical Sciences, Fudan University, 200438, Shanghai, China.

Collaborative Innovation Center for Biotherapy, West China Hospital, Sichuan University, 610041, Chengdu, China.

出版信息

Signal Transduct Target Ther. 2021 Feb 9;6(1):54. doi: 10.1038/s41392-020-00411-4.

Abstract

In addition to their use in relieving the symptoms of various diseases, ketogenic diets (KDs) have also been adopted by healthy individuals to prevent being overweight. Herein, we reported that prolonged KD exposure induced cardiac fibrosis. In rats, KD or frequent deep fasting decreased mitochondrial biogenesis, reduced cell respiration, and increased cardiomyocyte apoptosis and cardiac fibrosis. Mechanistically, increased levels of the ketone body β-hydroxybutyrate (β-OHB), an HDAC2 inhibitor, promoted histone acetylation of the Sirt7 promoter and activated Sirt7 transcription. This in turn inhibited the transcription of mitochondrial ribosome-encoding genes and mitochondrial biogenesis, leading to cardiomyocyte apoptosis and cardiac fibrosis. Exogenous β-OHB administration mimicked the effects of a KD in rats. Notably, increased β-OHB levels and SIRT7 expression, decreased mitochondrial biogenesis, and increased cardiac fibrosis were detected in human atrial fibrillation heart tissues. Our results highlighted the unknown detrimental effects of KDs and provided insights into strategies for preventing cardiac fibrosis in patients for whom KDs are medically necessary.

摘要

除了用于缓解各种疾病的症状外,生酮饮食(KDs)也被健康个体采用来预防超重。在此,我们报告了长期 KD 暴露会诱导心脏纤维化。在大鼠中,KD 或频繁的深度禁食会降低线粒体生物发生,降低细胞呼吸,并增加心肌细胞凋亡和心脏纤维化。在机制上,酮体β-羟丁酸(β-OHB)水平的升高,作为一种 HDAC2 抑制剂,促进了 Sirt7 启动子的组蛋白乙酰化,并激活了 Sirt7 的转录。这反过来又抑制了线粒体核糖体编码基因和线粒体生物发生的转录,导致心肌细胞凋亡和心脏纤维化。外源性的β-OHB 给药模拟了大鼠 KD 的作用。值得注意的是,在人类心房颤动心脏组织中检测到β-OHB 水平升高和 SIRT7 表达增加、线粒体生物发生减少和心脏纤维化增加。我们的研究结果强调了 KDs 的未知不良影响,并为预防因医学需要而采用 KDs 的患者的心脏纤维化提供了策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f743/7870678/c580b3e6f54a/41392_2020_411_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验