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20 周时高脂肪高果糖饮食诱导的大鼠肝脂肪变性的进展及其与肝线粒体结构和功能的关系和相互关系。

20-Week follow-up of hepatic steatosis installation and liver mitochondrial structure and activity and their interrelation in rats fed a high-fat-high-fructose diet.

机构信息

1DMEM,INRA,Univ. Montpellier,Montpellier,France.

2IATE,CIRAD,Montpellier,France.

出版信息

Br J Nutr. 2018 Feb;119(4):368-380. doi: 10.1017/S0007114517003713.

Abstract

The incidence of obesity and its metabolic complications are rapidly increasing and become a major public health issue. This trend is associated with an increase in the prevalence of non-alcoholic fatty liver disease (NAFLD), insulin resistance and diabetes. The sequence of events leading to NAFLD progression and mitochondrial dysfunction and their interrelation remains to be elucidated. This study aimed to explore the installation and progression of NAFLD and its association with the liver mitochondrial structure and activity changes in rats fed an obesogenic diet up to 20 weeks. Male Wistar rats were fed either a standard or high-fat-high-fructose (HFHFR) diet and killed on 4, 8, 12, 16 and 20 weeks of diet intake. Rats fed the HFHFR diet developed mildly overweight, associated with increased adipose tissue weight, hepatic steatosis, hyperglycaemia and hyperinsulinaemia after 8 weeks of HFHFR diet. Hepatic steatosis and many biochemical modifications plateaued at 8-12 weeks of HFHFR diet with slight amelioration afterwards. Interestingly, several biochemical and physiological parameters of mitochondrial function, as well as its phospholipid composition, in particular cardiolipin content, were tightly related to hepatic steatosis installation. These results showed once again the interrelation between hepatic steatosis development and mitochondrial activity alterations without being able to say whether the mitochondrial alterations preceded or followed the installation/progression of hepatic steatosis. Because both hepatic steatosis and mitochondrial alterations occurred as early as 4 weeks of diet, future studies should consider these four 1st weeks to reveal the exact interconnection between these major consequences of obesogenic diet intake.

摘要

肥胖及其代谢并发症的发病率迅速上升,成为一个主要的公共卫生问题。这种趋势与非酒精性脂肪性肝病(NAFLD)、胰岛素抵抗和糖尿病的患病率增加有关。导致 NAFLD 进展和线粒体功能障碍的事件顺序及其相互关系仍有待阐明。本研究旨在探索肥胖诱导饮食喂养大鼠 NAFLD 的发生和进展及其与肝脏线粒体结构和功能变化的关系,为期 20 周。雄性 Wistar 大鼠分别给予标准饮食或高脂肪高果糖(HFHFR)饮食,在摄入饮食 4、8、12、16 和 20 周时处死。给予 HFHFR 饮食的大鼠在 8 周后出现轻度超重,伴有脂肪组织重量增加、肝脂肪变性、高血糖和高胰岛素血症。8-12 周 HFHFR 饮食后,肝脂肪变性和许多生化改变趋于稳定,随后略有改善。有趣的是,几种线粒体功能的生化和生理参数及其磷脂组成,特别是心磷脂含量,与肝脂肪变性的发生密切相关。这些结果再次表明肝脂肪变性发展与线粒体活性改变之间的相互关系,但不能确定线粒体改变是先于还是后于肝脂肪变性的发生/进展。由于肝脂肪变性和线粒体改变早在饮食的第 4 周就已经发生,未来的研究应该考虑这最初的 4 周,以揭示肥胖诱导饮食摄入这两种主要后果之间的确切关联。

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