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无菌小鼠定植厚壁菌门,但不定植拟杆菌门,可通过调节肝内脂质代谢来加重非酒精性脂肪性肝病严重程度。

Gnotobiotic mice inoculated with Firmicutes, but not Bacteroidetes, deteriorate nonalcoholic fatty liver disease severity by modulating hepatic lipid metabolism.

机构信息

Graduate Institute of Veterinary Pathobiology, National Chung Hsing University, Taichung, 402, Taiwan.

Division of Animal Industry, Animal Technology Laboratories, Agricultural Technology Research Institute, Miaoli, 350, Taiwan.

出版信息

Nutr Res. 2019 Sep;69:20-29. doi: 10.1016/j.nutres.2019.07.001. Epub 2019 Jul 30.

DOI:10.1016/j.nutres.2019.07.001
PMID:31470288
Abstract

Nonalcoholic fatty liver disease (NAFLD) is a serious liver disorder and characterized by the hepatic accumulation of excess fatty acids. Clinical studies and animal models have shown a shift of gut microbiota from bacteroidetes to firmicutes in NAFLD patients and a diet-induced NAFLD mouse model. Therefore, we hypothesized that these 2 groups of bacteria may have differential effects on lipid metabolism in the liver, which further contributed to pathogenesis of NAFLD. To elucidate these effects, we inoculated two species of Bacteroidetes (B-group) or five species of Firmicutes (F-group) which were isolated from healthy individuals into germ-free mice. We found that the F-group induced elevated body weight, liver weight, and hepatic steatosis compared to the B-group under high-fat diet (HFD) conditions. The mRNA expression level of cluster of differentiation 36 (CD36) was elevated in the F-group compared to that in the B-group. Increased mRNA expression levels of fatty acid synthase (FAS), stearoyl-CoA desaturase-1 (SCD1), and diacylglycerol O-acyltransferase 2 (DGAT2) were also seen under HFD conditions in the F-group compared to that in the B-group. In addition, the expression level of miR802-5p was only elevated in the F-group under HFD conditions. Taken together, our results suggested that these specific species of Firmicutes may induce more hepatic steatosis by modulating fatty acid influx and lipogenesis compared to those of Bacteroidetes. These results may provide more understanding of the effects of gut microbiota on NAFLD.

摘要

非酒精性脂肪性肝病(NAFLD)是一种严重的肝脏疾病,其特征是肝脏中积聚过多的脂肪酸。临床研究和动物模型表明,NAFLD 患者和饮食诱导的 NAFLD 小鼠模型中,肠道微生物群从拟杆菌门向厚壁菌门转移。因此,我们假设这两组细菌可能对肝脏的脂质代谢有不同的影响,这进一步导致了 NAFLD 的发病机制。为了阐明这些影响,我们将从健康个体中分离出的两种拟杆菌(B 组)或五种厚壁菌(F 组)接种到无菌小鼠中。我们发现,与 B 组相比,F 组在高脂肪饮食(HFD)条件下诱导体重、肝重和肝脂肪变性升高。与 B 组相比,F 组的 CD36 基因表达水平升高。在 HFD 条件下,F 组的脂肪酸合酶(FAS)、硬脂酰辅酶 A 去饱和酶-1(SCD1)和二酰基甘油 O-酰基转移酶 2(DGAT2)的 mRNA 表达水平也升高。此外,只有在 HFD 条件下,F 组的 miR802-5p 表达水平升高。综上所述,我们的结果表明,与拟杆菌门相比,这些特定的厚壁菌门物种可能通过调节脂肪酸内流和脂肪生成来诱导更多的肝脂肪变性。这些结果可能为肠道微生物群对 NAFLD 的影响提供更多的了解。

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