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膳食铜-果糖相互作用改变雄性大鼠肠道微生物的活性。

Dietary copper-fructose interactions alter gut microbial activity in male rats.

机构信息

Department of Medicine, Division of Gastroenterology, Hepatology and Nutrition, University of Louisville School of Medicine , Louisville, Kentucky.

Hepatobiology and Toxicology Center, University of Louisville School of Medicine , Louisville, Kentucky.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2018 Jan 1;314(1):G119-G130. doi: 10.1152/ajpgi.00378.2016. Epub 2017 Oct 12.

Abstract

Dietary copper-fructose interactions contribute to the development of nonalcoholic fatty liver disease (NAFLD). Gut microbiota play critical roles in the pathogenesis of NAFLD. The aim of this study was to determine the effect of different dietary doses of copper and their interactions with high fructose on gut microbiome. Male weanling Sprague-Dawley rats were fed diets with adequate copper (6 ppm CuA), marginal copper (1.5 ppm CuM) (low copper), or supplemented copper (20 ppm CuS) (high copper) for 4 wk. Deionized water or deionized water containing 30% fructose (wt/vol) was given ad libitum. Copper status, liver enzymes, gut barrier function, and gut microbiome were evaluated. Both low- and high-copper diets led to liver injury in high-fructose-fed rats, and this was associated with gut barrier dysfunction, as shown by the markedly decreased tight junction proteins and increased gut permeability. 16S rDNA sequencing analysis revealed distinct alterations of the gut microbiome associated with dietary low- and high-copper/high-fructose feeding. The common features of the alterations of the gut microbiome were the increased abundance of Firmicutes and the depletion of Akkermansia. However, they differed mainly within the phylum Firmicutes. Our data demonstrated that a complex interplay among host, microbes, and dietary copper-fructose interaction regulates gut microbial metabolic activity, which may contribute to the development of liver injury and hepatic steatosis. The distinct alterations of gut microbial activity, which were associated with the different dietary doses of copper and fructose, imply that separate mechanism(s) may be involved. NEW & NOTEWORTHY First, dietary low- and high-copper/high-fructose-induced liver injury are associated with distinct alterations of gut microbiome. Second, dietary copper level plays a critical role in maintaining the gut barrier integrity, likely by acting on the intestinal tight junction proteins and the protective commensal bacteria Akkermansia. Third, the alterations of gut microbiome induced by dietary low and high copper with or without fructose differ mainly within the phylum Firmicutes.

摘要

饮食铜-果糖相互作用导致非酒精性脂肪性肝病(NAFLD)的发生。肠道微生物群在 NAFLD 的发病机制中起关键作用。本研究旨在确定不同饮食铜剂量及其与高果糖的相互作用对肠道微生物群的影响。雄性断奶 Sprague-Dawley 大鼠喂食 4 周含有足够铜(6 ppm CuA)、边缘铜(1.5 ppm CuM)(低铜)或补充铜(20 ppm CuS)(高铜)的饮食。自由给予去离子水或去离子水含 30%果糖(wt/vol)。评估铜状态、肝酶、肠道屏障功能和肠道微生物群。低铜和高铜饮食均可导致高果糖喂养大鼠的肝损伤,这与肠道屏障功能障碍有关,表现为紧密连接蛋白明显减少和肠道通透性增加。16S rDNA 测序分析显示,与饮食低铜和高铜/高果糖喂养相关的肠道微生物群发生明显改变。肠道微生物群改变的共同特征是厚壁菌门丰度增加和 Akkermansia 减少。然而,它们主要在厚壁菌门内存在差异。我们的数据表明,宿主、微生物和饮食铜-果糖相互作用之间的复杂相互作用调节肠道微生物代谢活性,这可能导致肝损伤和肝脂肪变性的发生。与不同饮食铜和果糖剂量相关的肠道微生物活性的明显改变表明,可能涉及不同的机制。新的和值得注意的是,首先,饮食低铜和高铜/高果糖诱导的肝损伤与肠道微生物群的明显改变有关。其次,饮食铜水平在维持肠道屏障完整性方面起着关键作用,可能通过作用于肠紧密连接蛋白和保护性共生菌 Akkermansia 来实现。第三,饮食低铜和高铜(无论是否含有果糖)诱导的肠道微生物群的改变主要在厚壁菌门内存在差异。

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9
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