The Protective Effect and Mechanism of a Phytochemical Extract from theWild Vegetable Shutou (Crateva unilocularis Buch.) against Acetaminophen-Induced Liver Injury in Mice

被引:0
作者
Shan, Meimei [1 ,2 ]
Ma, Qian [1 ,3 ]
Sun, Yilin [1 ,3 ]
Gao, Fengyi [2 ]
Cai, Shengbao [1 ]
机构
[1] Kunming Univ Sci & Technol, Fac Food Sci & Engn, Kunming 650500, Peoples R China
[2] Shangqiu Normal Univ, Coll Biol & Food, Shangqiu 476000, Peoples R China
[3] Northeast Agr Univ, Dept Food Sci, Harbin 150030, Peoples R China
基金
中国国家自然科学基金;
关键词
APAP; Crateva unilocularis Buch; liver damage; reactive oxygen species; NF-KAPPA-B; INDUCED ACUTE HEPATOTOXICITY; INHIBITING OXIDATIVE STRESS; SIGNALING PATHWAYS; ETHANOL EXTRACT; INFLAMMATION; FIBROSIS; GINSENOSIDE; APOPTOSIS; SAPONINS;
D O I
10.3390/foods12163109
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Acetaminophen (APAP) abuse is a common public health problem which can cause severe liver damage. However, strategies for dealing with this situation safely and effectively are very limited. The goal of the current work was to evaluate the protection and potential molecular mechanisms of an ethanol extract from shoots of the wild vegetable shutou (Crateva unilocularis Buch.) (ECS) against APAP-induced liver damage in mice. Mice orally received ECS for seven days (300 or 600 mg/kg b.w. per day) before being intraperitoneally injected with APAP (250 mg/kg). Results exhibited that ECS obviously decreased the content of alkaline phosphatase, alanine aminotransferase, aspartate transaminase, and malondialdehyde (p < 0.05). Catalase and superoxide dismutase were notably restored (p < 0.05), and the content of reduced glutathione was obviously increased (p < 0.05). Moreover, ECS significantly inhibited the secretion of interleukin-1 beta and tumor necrosis factor-alpha (p < 0.05). Further analyses of the mechanisms showed that ECS may alleviate oxidative stress in the liver by increasing the expression of the nuclear factor erythroid-2-related factor 2 and NADH quinone oxidoreductase 1 proteins, and may suppress liver inflammation by inhibiting the expression of the phosphorylated-inhibitor kappa B alpha/inhibitor kappa B alpha, phosphorylated-nuclear factor kappa B/nuclear factor kappa B, and cyclooxygenase-2 proteins. Meanwhile, ECS inhibited hepatocyte apoptosis by enhancing B-cell lymphoma gene 2 and suppressing Bcl-2-associated X protein. In summary, ECS may be used as a dietary supplement to prevent the liver damage caused by APAP abuse.
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页数:16
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