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补充饱和长链脂肪酸可维持小鼠肠道微生态平衡并减轻乙醇诱导的肝损伤。

Supplementation of saturated long-chain fatty acids maintains intestinal eubiosis and reduces ethanol-induced liver injury in mice.

作者信息

Chen Peng, Torralba Manolito, Tan Justin, Embree Mallory, Zengler Karsten, Stärkel Peter, van Pijkeren Jan-Peter, DePew Jessica, Loomba Rohit, Ho Samuel B, Bajaj Jasmohan S, Mutlu Ece A, Keshavarzian Ali, Tsukamoto Hidekazu, Nelson Karen E, Fouts Derrick E, Schnabl Bernd

机构信息

Department of Medicine, University of California San Diego, La Jolla, California.

J. Craig Venter Institute, Rockville, Maryland.

出版信息

Gastroenterology. 2015 Jan;148(1):203-214.e16. doi: 10.1053/j.gastro.2014.09.014. Epub 2014 Sep 16.

Abstract

BACKGROUND & AIMS: Alcoholic liver disease is a leading cause of mortality. Chronic alcohol consumption is accompanied by intestinal dysbiosis, and development of alcoholic liver disease requires gut-derived bacterial products. However, little is known about how alterations to the microbiome contribute to pathogenesis of alcoholic liver disease.

METHODS

We used the Tsukamoto-French mouse model, which involves continuous intragastric feeding of isocaloric diet or alcohol for 3 weeks. Bacterial DNA from the cecum was extracted for deep metagenomic sequencing. Targeted metabolomics assessed concentrations of saturated fatty acids in cecal contents. To maintain intestinal metabolic homeostasis, diets of ethanol-fed and control mice were supplemented with saturated long-chain fatty acids (LCFA). Bacterial genes involved in fatty acid biosynthesis, amounts of lactobacilli, and saturated LCFA were measured in fecal samples of nonalcoholic individuals and patients with active alcohol abuse.

RESULTS

Analyses of intestinal contents from mice revealed alcohol-associated changes to the intestinal metagenome and metabolome, characterized by reduced synthesis of saturated LCFA. Maintaining intestinal levels of saturated fatty acids in mice resulted in eubiosis, stabilized the intestinal gut barrier, and reduced ethanol-induced liver injury. Saturated LCFA are metabolized by commensal Lactobacillus and promote their growth. Proportions of bacterial genes involved in fatty acid biosynthesis were lower in feces from patients with active alcohol abuse than controls. Total levels of LCFA correlated with those of lactobacilli in fecal samples from patients with active alcohol abuse but not in controls.

CONCLUSIONS

In humans and mice, alcohol causes intestinal dysbiosis, reducing the capacity of the microbiome to synthesize saturated LCFA and the proportion of Lactobacillus species. Dietary approaches to restore levels of saturated fatty acids in the intestine might reduce ethanol-induced liver injury in patients with alcoholic liver disease.

摘要

背景与目的

酒精性肝病是导致死亡的主要原因。长期饮酒会伴随肠道微生物群失调,而酒精性肝病的发展需要肠道来源的细菌产物。然而,关于微生物群的改变如何导致酒精性肝病的发病机制,人们知之甚少。

方法

我们使用了筑本-弗伦奇小鼠模型,该模型包括连续3周经胃内给予等热量饮食或酒精。从盲肠提取细菌DNA进行深度宏基因组测序。靶向代谢组学评估盲肠内容物中饱和脂肪酸的浓度。为维持肠道代谢稳态,给乙醇喂养的小鼠和对照小鼠的饮食补充饱和长链脂肪酸(LCFA)。在非酒精个体和酒精滥用活跃患者的粪便样本中测量参与脂肪酸生物合成的细菌基因、乳酸杆菌数量和饱和LCFA。

结果

对小鼠肠道内容物的分析显示,酒精会导致肠道宏基因组和代谢组发生变化,其特征是饱和LCFA的合成减少。维持小鼠肠道中饱和脂肪酸水平可导致肠道微生态平衡,稳定肠道屏障,并减少乙醇诱导的肝损伤。饱和LCFA由共生乳酸杆菌代谢并促进其生长。酒精滥用活跃患者粪便中参与脂肪酸生物合成的细菌基因比例低于对照组。在酒精滥用活跃患者的粪便样本中,LCFA的总量与乳酸杆菌的总量相关,但在对照组中不相关。

结论

在人类和小鼠中,酒精会导致肠道微生物群失调,降低微生物群合成饱和LCFA的能力以及乳酸杆菌属的比例。恢复肠道中饱和脂肪酸水平的饮食方法可能会减少酒精性肝病患者乙醇诱导的肝损伤。

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