Trimethylamine N-oxide attenuates high-fat high-cholesterol dietinduced steatohepatitis by reducing hepatic cholesterol overload in rats

被引:0
作者
Ze-Hua Zhao [1 ]
Feng-Zhi Xin [1 ]
Da Zhou [1 ]
Ya-Qian Xue [2 ]
Xiao-Lin Liu [1 ]
Rui-Xu Yang [1 ]
Qin Pan [1 ]
Jian-Gao Fan [1 ,3 ]
机构
[1] Center for Fatty Liver, Department of Gastroenterology, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
[2] CAS Key Laboratory of Nutrition, Metabolism and Food Safety, Shanghai Institute of Nutrition and Health, Shanghai Institutes for Biological Sciences, University of Chinese Academy of Sciences, Chinese Academy of Sciences
[3] Shanghai Key Lab of Pediatric Gastroenterology and Nutrition
基金
中国国家自然科学基金;
关键词
Gut microbiota; Trimethylamine N-oxide; Nonalcoholic steatohepatitis; Endoplasmic reticulum stress; Cholesterol;
D O I
暂无
中图分类号
R575 [肝及胆疾病];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Trimethylamine N-oxide(TMAO) has been shown to be involved in cardiovascular disease(CVD). However, its role in nonalcoholic steatohepatitis(NASH) is unknown.AIM To determine the effect of TMAO on the progression of NASH.METHODS A rat model was induced by 16-wk high-fat high-cholesterol(HFHC) diet feeding and TMAO was administrated by daily oral gavage for 8 wk.RESULTS Oral TMAO intervention attenuated HFHC diet-induced steatohepatitis in rats.Histological evaluation showed that TMAO treatment significantly alleviated lobular inflammation and hepatocyte ballooning in the livers of rats fed a HFHC diet. Serum levels of alanine aminotransferase and aspartate aminotransferase were also decreased by TMAO treatment. Moreover, hepatic endoplasmic reticulum(ER) stress and cell death were mitigated in HFHC diet-fed TMAOtreated rats. Hepatic and serum levels of cholesterol were both decreased byTMAO treatment in rats fed a HFHC diet. Furthermore, the expression levels of intestinal cholesterol transporters were detected. Interestingly, cholesterol influxrelated Niemann-Pick C1-like 1 was downregulated and cholesterol efflux-related ABCG5/8 were upregulated by TMAO treatment in the small intestine. Gut microbiota analysis showed that TMAO could alter the gut microbial profile and restore the diversity of gut flora.CONCLUSION These data suggest that TMAO may modulate the gut microbiota, inhibit intestinal cholesterol absorption, and ameliorate hepatic ER stress and cell death under cholesterol overload, thereby attenuating HFHC diet-induced steatohepatitis in rats. Further studies are needed to evaluate the influence on CVD and define the safe does of TMAO treatment.
引用
收藏
页码:2450 / 2462
页数:13
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