Anwulignan Alleviates the Acute Liver Injury Induced by Acetaminophen in Mice

被引:1
作者
Zhao, Chenghe [1 ]
Wang, Yao [2 ]
Jing, Shu [3 ]
Lin, Huijiao [2 ]
Li, He [2 ]
Chen, Jianguang [2 ]
Xia, Wei [1 ]
机构
[1] Beihua Univ, Coll Med Technol, Dept Mol Biol Test Tech, Jilin, Peoples R China
[2] Beihua Univ, Coll Pharm, Dept Pharmacol, Jilin, Peoples R China
[3] Beihua Univ, Affiliated Hosp, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
Anwulignan; acetaminophen; liver injury; protective effect; apoptosis; SIGNALING PATHWAY; BCL-2;
D O I
10.1177/09731296231220116
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: Drug-induced liver injury (DILI) is extremely common in clinical practice and needs to be focused. Anwulignan is a unique lignan monomer of Schisandrae Sphenantherae Fructus and is used as the main active ingredient of Wuzhi tablet, which is used for liver protection in clinical practice. In this study, an acute liver injury mouse model induced by acetaminophen and paracetamol (APAP) was used to observe its effects.Materials and Methods: An acute liver injury mouse model was established by intraperitoneally injecting APAP. Mice were divided into blank control (CON) group, APAP model (MOD) group, Anwulignan CON group, and Anwulignan MOD group. Anwulignan (6 mg/kg) or sodium carboxymethylcellulose (10 mL/kg) was intragastrically given to mice once a day, successively for 14 days. On day 14, 250 mg/kg APAP solution (10 mL/kg) or saline was injected intraperitoneally, and 12 h later, the mice were killed. alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels in the serum of mice were tested. The liver index of mice was calculated, and the pathology of liver injury was evaluated by HE staining in mice. The activities of glutathione peroxidase (GSH-Px) and superoxide dismutase (SOD) as well as the content of malondialdehyde (MDA) in the liver tissue were tested. The levels of kelch-like ECH-associated protein 1 (Keap-1), nuclear factor erythroid-2-related factor 2 (Nrf2), heme oxygenase 1 (HO-1), BCL2 associated X protein (Bax), B-cell lymphoma-2 (Bcl-2), caspase-3 and tumor suppressor protein (P53) mRNAs in the liver tissues of mice were detected by reverse transcription-PCR (RT-PCR), and the expression levels of Keap-1, Nrf2, HO-1, Bax, Bcl-2, caspase-3 and P53 proteins in the liver tissue of mice were detected by Western blot.Results: Anwulignan can alleviate the acute liver injury of mice. The down-regulation of the cyclophosphamide (CYP2E1) expression in the liver tissue of mice to reduce the hepatotoxicity of APAP, and the regulation of Nrf2-ARE signaling pathway-related gene expressions to play an antioxidant role and apoptosis-related gene expressions to inhibit the liver cell apoptosis may be involved in the mechanism through which Anwulignan can exert its effect.Conclusion: Anwulignan can alleviate the liver injury induced by APAP in mice, and this study may provide evidence for researching and developing some drugs and nutraceuticals used for preventing and treating liver injury.
引用
收藏
页码:656 / 665
页数:10
相关论文
共 50 条
[21]   Hepatoprotective effect of chiisanoside against acetaminophen-induced acute liver injury in mice [J].
Bian, Xingbo ;
Wang, Shijie ;
Liu, Jinping ;
Zhao, Yan ;
Li, Haijun ;
Zhang, Lianxue ;
Li, Pingya .
NATURAL PRODUCT RESEARCH, 2019, 33 (18) :2704-2707
[22]   Protective effects of α-mangostin against acetaminophen-induced acute liver injury in mice [J].
Fu, Tianhua ;
Wang, Shijie ;
Liu, Jinping ;
Cai, Enbo ;
Li, Haijun ;
Li, Pingya ;
Zhao, Yan .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2018, 827 :173-180
[23]   Gut microbiota mediates diurnal variation of acetaminophen induced acute liver injury in mice [J].
Gong, Shenhai ;
Lan, Tian ;
Zeng, Liyan ;
Luo, Haihua ;
Yang, Xiaoyu ;
Li, Na ;
Chen, Xiaojiao ;
Liu, Zhanguo ;
Li, Rui ;
Win, Sanda ;
Liu, Shuwen ;
Zhou, Hongwei ;
Schnabl, Bernd ;
Jiang, Yong ;
Kaplowitz, Neil ;
Chen, Peng .
JOURNAL OF HEPATOLOGY, 2018, 69 (01) :51-59
[24]   Irbesartan mitigates acute liver injury, oxidative stress, and apoptosis induced by acetaminophen in mice [J].
Helal, Manar G. ;
Samra, Yara A. .
JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY, 2020, 34 (12)
[25]   Liuweiwuling tablets attenuate acetaminophen-induced acute liver injury and promote liver regeneration in mice [J].
Lei, Yan-Chang ;
Li, Wen ;
Luo, Pan .
WORLD JOURNAL OF GASTROENTEROLOGY, 2015, 21 (26) :8089-8095
[26]   Histopathological changes of acetaminophen-induced liver injury and subsequent liver regeneration in BALB/C and ICR mice [J].
Muhammad-Azam, Fazil ;
Nur-Fazila, Saulol Hamid ;
Ain-Fatin, Raslan ;
Noordin, Mohamed Mustapha ;
Yimer, Nurhusien .
VETERINARY WORLD, 2019, 12 (11) :1682-1688
[27]   Liuweiwuling tablets attenuate acetaminophen-induced acute liver injury and promote liver regeneration in mice [J].
Yan-Chang Lei ;
Wen Li ;
Pan Luo .
World Journal of Gastroenterology, 2015, (26) :8089-8095
[28]   GPR116 alleviates acetaminophen-induced liver injury in mice by inhibiting endoplasmic reticulum stress [J].
Xiang, Qian ;
Li, Na ;
Zhang, Yan ;
Wang, Ting ;
Wang, Ying ;
Bian, Jinjun .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2024, 81 (01)
[29]   Hepatoprotective effect of Diospyros lotus leaf extract against acetaminophen-induced acute liver injury in mice [J].
Byoung Ok Cho ;
Hong Hua Yin ;
Chong Zhou Fang ;
Sang Jun Kim ;
Seung Il Jeong ;
Seon Il Jang .
Food Science and Biotechnology, 2015, 24 :2205-2212
[30]   Hepatoprotective Effect of Ugonin M, A Helminthostachys zeylanica Constituent, on Acetaminophen-Induced Acute Liver Injury in Mice [J].
Wu, Kun-Chang ;
Ho, Yu-Ling ;
Kuo, Yueh-Hsiung ;
Huang, Shyh-Shyun ;
Huang, Guan-Jhong ;
Chang, Yuan-Shiun .
MOLECULES, 2018, 23 (10)