4.4 Article

Lactobacillus fermentum CQPC07 attenuates obesity, inflammation and dyslipidemia by modulating the antioxidant capacity and lipid metabolism in high-fat diet induced obese mice

期刊

JOURNAL OF INFLAMMATION-LONDON
卷 18, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12950-021-00272-w

关键词

Lactobacillus fermentum; Anti-inflammation; High-fat diet; Anti-obesity; Lipid metabolism

资金

  1. Chongqing University Innovation Research Group Project [CXQTP20033]
  2. Science and Technology Project of Chongqing Education Commission [KJQN202001604]

向作者/读者索取更多资源

The study showed that the Lactobacillus fermentum CQPC07 (LF-CQPC07) isolated from pickled vegetables effectively controlled weight gain caused by a high-fat diet in mice. LF-CQPC07 reduced levels of cholesterol and triglycerides, decreased inflammatory cytokines, and increased anti-inflammatory cytokines, improving lipid metabolism and liver health in obese mice. This suggests that LF-CQPC07 has great potential as a probiotic for preventing and treating obesity.
BackgroundObesity is an epidemic disease in the world, the treatment and prevention of obesity methods have gained great attention. Lactobacillus is the main member of probiotics, and the physiological activity of it is specific to different strains. This study systematically explored the anti-obesity effect and possible mechanism of Lactobacillus fermentum CQPC07 (LF-CQPC07), which was isolated from pickled vegetables.ResultsLF-CQPC07 effectively controlled the weight gain of mice caused by a high-fat diet. The results of pathological sections indicated that LF-CQPC07 alleviated hepatocyte damage and fat accumulation in adipocytes. The detection of biochemical indictors revealed that LF-CQPC07 decreased the levels of total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), and triglycerides (TG), and increased the level of high-density lipoprotein cholesterol (HDL-C). Additionally, LF-CQPC07 caused the decrease in the amounts of inflammatory cytokines interleukin (IL)-1 beta, tumor necrosis factor-alpha (TNF-alpha), IL-6, and interferon-gamma (IFN-gamma), and the increase in the amounts of the anti-inflammatory cytokines IL-10 and IL-4. LF-CQPC07 also decreased the amounts of alanine aminotransferase (ALT), aspartate transaminase (AST), and alkaline phosphatase (ALP). Confirmed by qPCR, LF-CQPC07 enhanced the mRNA expression of catalase (CAT), gamma glutamylcysteine synthetase 1 (GSH1), copper/zinc superoxide dismutase (SOD1), manganese superoxide dismutase (SOD2), and glutathione peroxidase (GSH-Px). It also increased the mRNA expression levels of carnitine palmitoyltransferase 1 (CPT1), peroxisome proliferator-activated receptor alpha (PPAR-alpha), lipoprotein lipase (LPL), and cholesterol 7 alpha hydroxylase (CYP7A1), and decreased that of PPAR-gamma and CCAAT/enhancer binding protein alpha (C/EBP-alpha) in the liver of mice.ConclusionThis research confirmed that LF-CQPC07 is capable of ameliorating obesity, improving hyperlipemia, and alleviating chronic low-grade inflammation and liver injury accompanied with obesity. Its mechanism may be the regulation of antioxidant capacity and lipid metabolism. Therefore, LF-CQPC07 has enormous potential to serve as a potential probiotic for the prevention or treatment of obesity.

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