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小鼠硫代乙酰胺诱导肝硬化中昼夜代谢组分析

Profiling of the circadian metabolome in thioacetamide-induced liver cirrhosis in mice.

作者信息

Fujisawa Koichi, Takami Taro, Matsumoto Toshihiko, Yamamoto Naoki, Sakaida Isao

机构信息

Center for Regenerative Medicine Yamaguchi University School of Medicine Ube Yamaguchi Japan.

Department of Gastroenterology and Hepatology Yamaguchi University Graduate School of Medicine Ube Yamaguchi Japan.

出版信息

Hepatol Commun. 2017 Jul 26;1(7):704-718. doi: 10.1002/hep4.1075. eCollection 2017 Sep.

Abstract

Liver cirrhosis can disturb circadian rhythms, decreasing patient quality of life. Changes in metabolic products in cirrhosis are poorly understood. We evaluated changes in liver metabolism products using a thioacetamide-induced mouse model of liver cirrhosis exhibiting circadian rhythm disturbance. Principal component analysis indicated that the circular progression found in the control group was disrupted in the thioacetamide group, and Jonckheere-Terpstra-Kendall analysis showed an imbalanced pattern of oscillating metabolic products. In addition to changes in serotonin and other vitamin A-related metabolites, differences in metabolic products associated with energetics, redox homeostasis, bile acid production, inflammation, and other processes were identified. Carbohydrate metabolism showed a reduction in metabolic products associated with the tricarboxylic acid cycle, suggesting up-regulation of glycolysis and reduced mitochondrial activity. Lipid metabolism showed an increase in ω-oxidation products, suggesting decreased β-oxidation. : These data will be useful for chronotherapy and modulation of circadian rhythms in patients with liver damage. ( 2017;1:704-718).

摘要

肝硬化会扰乱昼夜节律,降低患者生活质量。目前对肝硬化中代谢产物的变化了解甚少。我们使用硫代乙酰胺诱导的表现出昼夜节律紊乱的肝硬化小鼠模型,评估了肝脏代谢产物的变化。主成分分析表明,对照组中发现的循环进程在硫代乙酰胺组中被破坏,琼克海尔-特普斯特拉-肯德尔分析显示振荡代谢产物的模式失衡。除了血清素和其他与维生素A相关的代谢产物变化外,还发现了与能量代谢、氧化还原稳态、胆汁酸生成、炎症及其他过程相关的代谢产物差异。碳水化合物代谢显示与三羧酸循环相关的代谢产物减少,提示糖酵解上调且线粒体活性降低。脂质代谢显示ω-氧化产物增加,提示β-氧化减少。这些数据将有助于对肝损伤患者进行时间治疗和昼夜节律调节。(2017;1:704 - 718)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d57c/5721444/805c1cfb9e0d/HEP4-1-704-g001.jpg

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