Induction mechanism of cigarette smoke components (CSCs) on dyslipidemia and hepatic steatosis in rats
文献类型: 外文期刊
作者: Ge, Jian 1 ; Xu, Wei-jia 1 ; Chen, Hai-feng 1 ; Dong, Zong-hua 1 ; Liu, Wei 3 ; Nian, Fu-zhao 2 ; Liu, Jun 1 ;
作者机构: 1.China Jiliang Univ, Coll Life Sci, XiaSha Higher Educ Zone, 258 XueYuan St, Hangzhou 310018, Zhejiang, Peoples R China
2.Yunnan Agr Univ, Coll Tobacco Sci, Kunming 650201, Yunnan, Peoples R China
3.Zhejiang Acad Agr Sci, Inst Microbiol, Hangzhou 310021, Zhejiang, Peoples R China
关键词: Cigarette smoke components (CSC); Dyslipidemia; Gut microbiota; Serum exosomes; miRNA regulation
期刊名称:LIPIDS IN HEALTH AND DISEASE ( 影响因子:4.315; 五年影响因子:4.622 )
ISSN:
年卷期: 2022 年 21 卷 1 期
页码:
收录情况: SCI
摘要: Objective The purpose of this study was to explore the effect of cigarette smoke component (CSC) exposure on serum lipid levels in rats and the underlying molecular mechanism. Methods Male SPF-grade SD rats were randomly divided into a control group and a CSC exposure group, with the CSC group being exposed to CSC for 6 weeks. RT-PCR and Western blotting methods were used to detect lipid metabolism gene expression in rats, and 16S RNA gene sequencing was used to detect the gut microbiota in the rat cecum. Rat serum exosomes were prepared and identified, and the interaction of exosomal miR-291a-3p and miR-126a-5p with AMPK and CYP7A1 was detected by a dual luciferase reporter gene assay (DLRG). Results Serum indicators, including cholesterol levels and trimethylamine oxide (TMAO) content, were significantly affected in the CSC exposure group compared with the control group (P < 0.05), and the expression levels of adenylate-activated protein kinase (AMPK), acetyl-coenzyme A carboxylase (ACC) and HMG-CoA reductase (HMG-CoAR) genes were significantly increased (P < 0.05) in the liver, while the expression level of cholesterol 7 alpha-hydroxylase (CYP7A1) was markedly decreased (P < 0.01). 16S rRNA gene sequencing of the gut microbiota in the rat cecum showed that the abundance of Firmicutes in the CSC group increased significantly at the phylum level, while the abundances of Bacteroidota and Spirochaetota were reduced significantly (P < 0.01). The relative abundance of Romboutsia, Turicibacter, and Clostridium sensu stricto increased significantly (P < 0.01), and the relative abundance of Prevotella, Muribaculaceae_norank, Lachnospiraceae NK4A136 group, Roseburia, Treponema, and Ruminococcus significantly decreased (P < 0.01) at the genus level. In addition, the exosome miR-291a-3p and miR-126a-5p levels were markedly regulated by CSC exposure (P < 0.01). The interactions of miR-291a-3p and miR-126a-5p with AMPK and CYP7A1 mRNA were also validated by the DLRG method. Conclusions In summary, the rat dyslipidemia induced by CSC exposure may be related to the interference of gut microbiota structure and interaction of miRNAs from serum exosomes with target mRNAs, which further regulated AMPK-ACC/CYP7A1 signaling in rats.
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