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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).
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页码:15154 / 15163
页数:10
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