Protective Effect of Flavonoids from Ziziphus jujuba cv. Jinsixiaozao against Acetaminophen-Induced Liver Injury by Inhibiting Oxidative Stress and Inflammation in Mice

被引:45
|
作者
Huang, Weizhen [1 ]
Wang, Yongjie [1 ]
Jiang, Xiaoyan [1 ]
Sun, Yueyue [1 ]
Zhao, Zhongxi [1 ,2 ,3 ]
Li, Siying [4 ]
机构
[1] Shandong Univ, Sch Pharmaceut Sci, 44 West Wenhua Rd, Jinan 250012, Shandong, Peoples R China
[2] Shandong Engn & Technol Res Ctr Jujube Food & Dru, 44 West Wenhua Rd, Jinan 250012, Shandong, Peoples R China
[3] Shandong Acad Pharmaceut Sci, Shandong Prov Key Lab Mucosal & Transdermal Drug, 989 Xinluo St, Jinan 250101, Shandong, Peoples R China
[4] Shandong Univ, Sch Basic Med, Dept Pathol & Pathophysiol, 44 West Wenhua Rd, Jinan 250012, Shandong, Peoples R China
关键词
Ziziphus jujuba cv. Jinsixiaozao; Flavonoids; hepatoprotective; antioxidant activity; Nrf2; anti-inflammation; NF-kappa B; ZIZYPHUS-JUJUBA; IN-VITRO; HEPATOPROTECTIVE ACTIVITY; ANTIOXIDATIVE ACTIVITIES; INDUCED HEPATOTOXICITY; DIETARY FLAVONOIDS; NATURAL-PRODUCTS; FRUITS; CELLS; MILL;
D O I
10.3390/molecules22101781
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This study was aimed to investigate the chemical composition, antioxidant activities and hepatoprotective effect of flavonoids from Ziziphus jujuba cv. Jinsixiaozao (ZJF). The composition of ZJF was analyzed by high performance liquid chromatography (HPLC) and Liquid chromatography-mass spectrometry (LC-MS), and antioxidant properties were investigated by biological assays in vitro. The hepatoprotective activity of ZJF was evaluated in acetaminophen (APAP)-treated BALB/c mice. Results indicate that ZJF displayed significant antioxidant capacity. Pretreatment with ZJF significantly decreased APAP-elevated serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP) and total bilirubin (TB). Activities of superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) were enhanced with ZJF administration, while malondialdehyde (MDA) level and glutathione (GSH) depletion were reduced. Meanwhile, ZJF reversed the suppression of nuclear factor erythroid 2-related factor 2 (Nrf2) nuclear translocation, and up-regulated the protein expression of NAD(P)H: quinone oxidoreductase 1(NQO1) in liver damage mice. Furthermore, ZJF attenuated APAP-induced inflammatory mediator production, such as nitric oxide (NO), tumor necrosis factor-alpha (TNF-alpha), interleukin-6 (IL-6) and interleukin-1 beta (IL-1 beta). Expression of p65 showed that ZJF dampened nuclear factor-kappa B (NF-kappa B) activation. The results strongly indicate that the hepatoprotective role of ZJF in APAP-induced hepatotoxicity might result from its induction of antioxidant defense via activation of Nrf2 and reduction of inflammation via inhibition of NF-kappa B.
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页数:18
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