生酮饮食通过平衡线粒体动力学和改善线粒体功能障碍来改善代谢相关脂肪性肝病。
Ketogenic diet ameliorates MASLD via balancing mitochondrial dynamics and improving mitochondrial dysfunction.
作者信息
You Yuehua, Ni Hongbin, Ma Qin, Jiang Lincheng, Cai Jingshu, He Wenjun, Lin Xiaojing, Li Kemeng, Wang Zhuyun, Yan Weiyan, Xiao Xiaoqiu, Ma Li
机构信息
Department of Endocrinology, Sichuan-Chongqing Joint Key Laboratory of Metabolic Vascular Diseases, Chongqing Key Laboratory of Translational Medicine in Major Metabolic Diseases, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Department of Nutrition and Food Hygiene, School of Public Health and Management, Chongqing Medical University, Chongqing, 400016, China.
出版信息
Nutr Diabetes. 2025 Aug 25;15(1):37. doi: 10.1038/s41387-025-00391-w.
BACKGROUND & AIMS: Ketogenic diet (KD) is recognized as an effective lifestyle intervention for managing metabolic dysfunction-associated steatotic liver disease (MASLD). This research aimed to assess the impact of KD on metabolic parameters in MASLD mice and elucidate the underlying mechanism.
METHODS
High-fat diet (HFD)-induced MASLD mice were subjected to KD for 2 weeks. Researchers measured hepatic fat, plasma Alanine Aminotransferase (ALT), and Aspartate Aminotransferase (AST) levels to assess metabolic changes. Hepatic mitochondrial dynamics were examined using transmission electron microscopy and Western blot. Mitochondrial functions were evaluated through Quantitative Polymerase Chain Reaction (qPCR) and measurement of ATP content. In vitro, HepG2 cells were treated with palmitate (PA), β-hydroxybutyric acid (β-OHB), and/or the mitochondrial fusion inhibitor MFI8 to study mitochondrial morphology, function, and lipid deposition.
RESULTS
KD feeding partially improved the MASLD phenotype and reduced Fission 1 protein (Fis1) and Dynamin-related protein 1 (Drp1) levels in the livers of MASLD mice. Additionally, KD ameliorated HFD-stimulated mitochondrial dysfunctions, as evidenced by elevated ATP levels and upregulation of key genes responsible for fatty-acid-oxidation. β-OHB mitigated PA-stimulated mitochondrial dysfunction and fission in HepG2 cells. Furthermore, β-OHB attenuated PA-stimulated lipid deposition, with this effect being counteracted by MFI8.
CONCLUSIONS
Our study suggests that a 2-week KD partially alleviates lipid deposition, restores mitochondrial dynamics balance, and improves mitochondrial dysfunctions in the livers of MASLD mice.
背景与目的
生酮饮食(KD)被认为是管理代谢功能障碍相关脂肪性肝病(MASLD)的一种有效生活方式干预措施。本研究旨在评估KD对MASLD小鼠代谢参数的影响,并阐明其潜在机制。
方法
对高脂饮食(HFD)诱导的MASLD小鼠进行2周的KD干预。研究人员测量肝脏脂肪、血浆丙氨酸转氨酶(ALT)和天冬氨酸转氨酶(AST)水平,以评估代谢变化。使用透射电子显微镜和蛋白质免疫印迹法检测肝脏线粒体动力学。通过定量聚合酶链反应(qPCR)和ATP含量测定评估线粒体功能。在体外,用棕榈酸(PA)、β-羟基丁酸(β-OHB)和/或线粒体融合抑制剂MFI8处理HepG2细胞,以研究线粒体形态、功能和脂质沉积。
结果
KD喂养部分改善了MASLD小鼠的表型,并降低了MASLD小鼠肝脏中裂变1蛋白(Fis1)和动力相关蛋白1(Drp1)的水平。此外,KD改善了HFD刺激的线粒体功能障碍,ATP水平升高和负责脂肪酸氧化的关键基因上调证明了这一点。β-OHB减轻了PA刺激的HepG2细胞线粒体功能障碍和裂变。此外,β-OHB减轻了PA刺激的脂质沉积,而MFI8可抵消这种作用。
结论
我们的研究表明,为期2周的KD可部分减轻MASLD小鼠肝脏中的脂质沉积,恢复线粒体动力学平衡,并改善线粒体功能障碍。
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