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饮食对小鼠肝脏中参与脂质代谢、氧化应激和炎症的基因表达的影响——对肝脂肪变性机制的深入了解

Effect of diet on expression of genes involved in lipid metabolism, oxidative stress, and inflammation in mouse liver-insights into mechanisms of hepatic steatosis.

作者信息

Renaud Helen J, Cui Julia Y, Lu Hong, Klaassen Curtis D

机构信息

Department of Internal Medicine, Kansas University Medical Center, Kansas City, Kansas, United States of America.

Department of Pharmacology, State University of New York, Syracuse, New York, United States of America.

出版信息

PLoS One. 2014 Feb 14;9(2):e88584. doi: 10.1371/journal.pone.0088584. eCollection 2014.

Abstract

Nutritional intake is a fundamental determinant of health. Many studies have correlated excess caloric intake, as well as a high ratio of n-6:n-3 fatty acids, with detrimental health outcomes, such as the metabolic syndrome. In contrast, low-calorie diets have beneficial health effects. Despite these associations, our understanding of the causal relationship between diet and health remains largely elusive. The present study examined the molecular changes elicited by nine diets with varying fat, sugar, cholesterol, omega-3 fatty acids, omega-6 fatty acids, and calories in C57BL/6 male mice. Microarray analyses were conducted on liver samples from three mice per diet and detected 20,449 genes of which 3,734 were responsive to changes in dietary components. Principal component analysis showed that diet restriction correlated the least with the other diets and also affected more genes than any other diet. Interestingly, Gene Set Enrichment Analysis (GSEA) identified gene sets involved in glutathione metabolism, immune response, fatty acid metabolism, cholesterol metabolism, ABC transporters, and oxidative phosphorylation as being highly responsive to changes in diet composition. On the gene level, this study reveals novel findings such as the induction of the drug efflux pump Abcb1a (p-glycoprotein) by diet restriction and an atherogenic diet, as well as the suppression of the rate limiting step of bile acid synthesis, Cyp7a1, by a high fructose diet. This study provides considerable insight into the molecular changes incurred by a variety of diets and furthers our understanding of the causal relationships between diet and health.

摘要

营养摄入是健康的一个基本决定因素。许多研究已将热量摄入过多以及n-6:n-3脂肪酸的高比例与有害的健康结果(如代谢综合征)联系起来。相比之下,低热量饮食对健康有有益影响。尽管存在这些关联,但我们对饮食与健康之间因果关系的理解在很大程度上仍然难以捉摸。本研究检测了C57BL/6雄性小鼠食用九种脂肪、糖、胆固醇、ω-3脂肪酸、ω-6脂肪酸和热量各不相同的饮食后引发的分子变化。对每种饮食的三只小鼠的肝脏样本进行了微阵列分析,检测到20449个基因,其中3734个基因对饮食成分的变化有反应。主成分分析表明,饮食限制与其他饮食的相关性最小,且比其他任何饮食影响的基因更多。有趣的是,基因集富集分析(GSEA)确定参与谷胱甘肽代谢、免疫反应、脂肪酸代谢、胆固醇代谢、ABC转运蛋白和氧化磷酸化的基因集对饮食组成的变化高度敏感。在基因水平上,本研究揭示了一些新发现,如饮食限制和致动脉粥样硬化饮食诱导药物外排泵Abcb1a(P-糖蛋白),以及高果糖饮食抑制胆汁酸合成的限速步骤Cyp7a1。这项研究为各种饮食引起的分子变化提供了相当多的见解,并加深了我们对饮食与健康之间因果关系的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f86/3925138/bd9f7b260065/pone.0088584.g001.jpg

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