首页> 外文期刊>The British Journal of Nutrition >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
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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

机译:肝脏脂肪变性安装和肝脏线粒体结构和活性的20周随访及其在大鼠中的相互关联喂养高脂肪高果糖饮食

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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.
机译:肥胖的发病率及其代谢并发症正在迅速增加,并成为一个主要的公共卫生问题。这种趋势与非酒精性脂肪肝疾病(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及其相互关联的事件序列仍有待阐明。本研究旨在探讨NAFLD的安装和进展及其与肝脏线粒体结构的关联,大鼠富含血液营养饮食的大鼠的活性变化长达20周。雄性Wistar大鼠喂食标准或高脂高果糖(HFHFR)饮食,并在4,8,12,16和20周内杀死饮食摄入量。喂养HFHFR饮食的大鼠显得轻度超重,与HFHFR饮食8周后的脂肪组织重量,肝脏脂肪变性,高血糖和高胰岛素血症相关。肝脏脂肪变性和许多生物化学修饰在8-12周的HFHFR饮食中有效,之后略有改善。有趣的是,微粒功能的几种生物化学和生理参数,以及其磷脂组合物,特别是心肝脂含量,与肝脏脂肪变性安装紧密相关。这些结果再次表现出肝脏脂肪变性发展和线粒体活性改变之间的相互关系,而不能够说出先前或遵循肝脏脂肪化的安装/进展的线粒体改变。由于肝脏脂肪变性和线粒体改变都早在饮食的4周内发生,因此未来的研究应该考虑这四个星期,以揭示令人生作的饮食摄入量的这些主要后果之间的确切互连。

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