Novel insights and mechanisms of diet-induced obesity: Mid-term versus long-term effects on hepatic transcriptome and antioxidant capacity in Sprague-Dawley rats.

Alejandro García-Beltrán, R. Martínez, J. Porres, F. Arrebola, Inmaculada Ruiz Artero, M. Galisteo, P. Aranda, G. Kapravelou, M. López-Jurado
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Abstract

AIMS The study of molecular mechanisms related to obesity and associated pathologies like type 2-diabetes and non-alcoholic fatty liver disease requires animal experimental models in which the type of obesogenic diet and length of the experimental period to induce obesity deeply affect the metabolic alterations. Therefore, this study aimed to test the influence of aging along a rat model of diet-induced obesity in gene expression of the hepatic transcriptome. MAIN METHODS A high-fat/high-fructose diet to induce obesity was used. Mid- (13 weeks) and long-term (21 weeks) periods were established. Caloric intake, bodyweight, hepatic fat, fatty acid profile, histological changes, antioxidant activity, and complete transcriptome were analyzed. KEY FINDINGS Excess bodyweight, hepatic steatosis and altered lipid histology, modifications in liver antioxidant activity, and dysregulated expression of transcripts related to cell structure, glucose & lipid metabolism, antioxidant & detoxifying capacity were found. Modifications in obese and control rats were accounted for by the different lengths of the experimental period studied. SIGNIFICANCE Main mechanisms of hepatic fat accumulation were de novo lipogenesis or altered fatty acid catabolism for mid- or long-term study, respectively. Therefore, the choice of obesity-induction length is a key factor in the model of obesity used as a control for each specific experimental design.
饮食诱导肥胖的新见解和机制:Sprague-Dawley大鼠肝脏转录组和抗氧化能力的中期和长期影响。
目的:肥胖及2型糖尿病、非酒精性脂肪性肝病等相关病理的分子机制研究需要动物实验模型,在动物实验模型中,致肥饮食的类型和诱导肥胖的实验时间长度深刻影响代谢改变。因此,本研究旨在通过饮食诱导的肥胖大鼠模型测试衰老对肝脏转录组基因表达的影响。主要方法采用高脂/高果糖饮食诱导肥胖。建立中期(13 周)和长期(21 周)。分析了热量摄入、体重、肝脏脂肪、脂肪酸谱、组织学变化、抗氧化活性和完整转录组。主要发现:体重超重、肝脏脂肪变性和脂质组织学改变、肝脏抗氧化活性改变以及与细胞结构、糖脂代谢、抗氧化和解毒能力相关的转录物表达失调。肥胖大鼠和对照组大鼠的变化是由实验时间长短不同引起的。意义肝脏脂肪积累的主要机制分别为中期和长期的脂肪生成和脂肪酸分解代谢的改变。因此,肥胖诱导长度的选择是每个特定实验设计中用作控制的肥胖模型的关键因素。
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