Pediococcus pentosaceus PP04 Ameliorates High-Fat Diet-Induced Hyperlipidemia by Regulating Lipid Metabolism in C57BL/6N Mice

被引:52
|
作者
Wang, Yu [1 ,2 ]
You, Ying [1 ,2 ]
Tian, Yuan [1 ,2 ]
Sun, Haiyue [1 ,2 ]
Li, Xia [1 ,2 ]
Wang, Xiujuan [1 ,2 ]
Wang, Yuhua [1 ,2 ,3 ,4 ]
Liu, Jingsheng [1 ,3 ]
机构
[1] Jilin Agr Univ, Coll Food Sci & Engn, Changchun 130118, Jilin, Peoples R China
[2] Jilin Agr Univ, Jilin Prov Innovat Ctr Food Biol Manufacture, Changchun 130118, Jilin, Peoples R China
[3] Natl Engn Lab Wheat & Corn Deep Proc, Changchun 130118, Peoples R China
[4] Natl Proc Lab Soybean Ind & Technol, Changchun 130118, Peoples R China
基金
国家重点研发计划;
关键词
Pediococcus pentosaceus PP04; hyperlipidemia; AMPK signaling pathway; oxidative stress; LACTIC-ACID BACTERIA; LIVER-DISEASE; PROBIOTIC PROPERTIES; OBESITY; FERMENTATION;
D O I
10.1021/acs.jafc.0c05060
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
In this study, Pediococcus pentococcus PP04 isolated from the Northeast pickled cabbage had good gastrointestinal tolerance and can colonize in the intestine stably. C57BL/6N mice were fed a high-fat diet to build animal models and treated with Pediococcus pentosaceus PP04 to evaluate the antihyperlipidemia effect. After 8 weeks, the indicators of hyperlipidemia, liver injury, and inflammation were measured. The treatment of P. pentosaceus PP04 reduced the gain of total cholesterol (TC), triglycerides (TG), low-density lipoprotein cholesterol (LDL-C), free fatty acids (FFAs), leptin, alanine aminotransferase (ALT), aspartate aminotransferase (AST), lipopolysaccharides (LPS), and tumor necrosis factor-alpha (TNF-alpha) significantly. The western blotting results suggested P. pentosaceus PP04 ameliorated high-fat diet-induced hyperlipidemia by the AMPK signaling pathway, which stimulated lipolysis via upregulation of PPAR alpha and inhibited lipogenesis by downregulation of SREBP-1c, fatty acid synthase (FAS), and stearoyl-CoA desaturase-1 (SCD1) mainly. Furthermore, P. pentosaceus PP04 improved high-fat diet-induced oxidative stress effectively by triggering the Nrf2/CYP2E1 signaling pathway that enhanced the antioxidant activity including superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px).
引用
收藏
页码:15154 / 15163
页数:10
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