Aged Citrus Peel (Chenpi) Prevents Acetaminophen-Induced Hepatotoxicity by Epigenetically Regulating Nrf2 Pathway

被引:32
作者
Lin, Zi-Han [1 ]
Chan, Yen-Fan [1 ]
Pan, Min-Hsiung [2 ,3 ,4 ]
Tung, Yen-Chen [2 ]
Su, Zheng-Yuan [1 ]
机构
[1] Chung Yuan Christian Univ, Dept Biosci Technol, 200 Chung Pei Rd, Taoyuan 32023, Taiwan
[2] Natl Taiwan Univ, Inst Food Sci & Technol, Taipei, Taiwan
[3] China Med Univ, China Med Univ Hosp, Dept Med Res, Taichung, Taiwan
[4] Asia Univ, Dept Hlth & Nutr Biotechnol, Taichung, Taiwan
来源
AMERICAN JOURNAL OF CHINESE MEDICINE | 2019年 / 47卷 / 08期
关键词
Acetaminophen; Aged Citrus Peel; Hepatotoxicity; Epigenetics; Liver; Nrf2; INDUCED OXIDATIVE STRESS; DIETARY PHYTOCHEMICALS; CELLS; METHYLATION; MECHANISMS; PROTECTS; CURCUMIN; TISSUES;
D O I
10.1142/S0192415X19500939
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Excessive consumption of analgesic drug acetaminophen (APAP) can cause severe oxidative stress-mediated liver injury. Here, we investigated the protective effect and mechanism of aged citrus peel (Chenpi, CP), a Chinese herb usually used in foods in Asia, against APAP-induced hepatotoxicity. CP water (CP-WE), ethanolic (CP-EE), and water extraction residue ethanolic (CP-WREE) extracts were prepared. We found that CP-WREE contained higher content of bioactive flavonoids, including narirutin, nobiletin, and tangeretin, and more effectively enhanced the Nrf2 pathway in ARE-luciferase reporter gene transfected human HepG2-C8 cells. In mouse AML-12 hepatocytes, CP-WREE minimized APAP-induced damage and lipid peroxidation and increased mRNA and protein expressions of Nrf2 and its downstream defense enzymes (HO-1, NQO1, and UGT1A). CP-WREE also downregulated HDACs and DNMTs, upregulated KDMs, and increased the unmethylated Nrf2 promoter level. Additionally, CP-WREE blocked in vitro DNA methyltransferase activity. Taken together, CP-WREE might attenuate oxidative stress-induced hepatotoxicity through epigenetically regulating Nrf2-mediated cellular defense system.
引用
收藏
页码:1833 / 1851
页数:19
相关论文
共 34 条
  • [1] Overexpression of Aldose Reductase Render Mouse Hepatocytes More Sensitive to Acetaminophen Induced Oxidative Stress and Cell Death
    Ahmed M.M.E.
    Al-Obosi J.A.S.
    Osman H.M.
    Shayoub M.E.
    [J]. Indian Journal of Clinical Biochemistry, 2016, 31 (2) : 162 - 170
  • [2] Aldo-Keto Reductase-7A Protects Liver Cells and Tissues From Acetaminophen-Induced Oxidative Stress and Hepatotoxicity
    Ahmed, Munzir M. E.
    Wang, Tao
    Luo, Yu
    Ye, Shuilong
    Wu, Qiao
    Guo, Zongsheng
    Roebuck, Bill D.
    Sutter, Thomas R.
    Yang, James Y.
    [J]. HEPATOLOGY, 2011, 54 (04) : 1322 - 1332
  • [3] Estimation of total phenolic content and other oxidation substrates in plant tissues using Folin-Ciocalteu reagent
    Ainsworth, Elizabeth A.
    Gillespie, Kelly M.
    [J]. NATURE PROTOCOLS, 2007, 2 (04) : 875 - 877
  • [4] Regulation of chromatin by histone modifications
    Bannister, Andrew J.
    Kouzarides, Tony
    [J]. CELL RESEARCH, 2011, 21 (03) : 381 - 395
  • [5] Histone Lysine Methylation Dynamics: Establishment, Regulation, and Biological Impact
    Black, Joshua C.
    Van Rechem, Capucine
    Whetstine, Johnathan R.
    [J]. MOLECULAR CELL, 2012, 48 (04) : 491 - 507
  • [6] Chang CC, 2002, J FOOD DRUG ANAL, V10, P178
  • [7] Cheng David, 2016, Current Opinion in Toxicology, V1, P134, DOI 10.1016/j.cotox.2016.10.008
  • [8] In Vitro Lipophilic Antioxidant Capacity, Antidiabetic and Antibacterial Activity of Citrus Fruits Extracts from Aceh, Indonesia
    Ernawita
    Wahyuono, Ruri Agung
    Hesse, Jana
    Hipler, Uta-Christina
    Elsner, Peter
    Boehm, Volker
    [J]. ANTIOXIDANTS, 2017, 6 (01)
  • [9] The Chemistry and Pharmacology of Citrus Limonoids
    Gualdani, Roberta
    Cavalluzzi, Maria Maddalena
    Lentini, Giovanni
    Habtemariam, Solomon
    [J]. MOLECULES, 2016, 21 (11)
  • [10] Curcumin inhibits anchorage-independent growth of HT29 human colon cancer cells by targeting epigenetic restoration of the tumor suppressor gene DLEC1
    Guo, Yue
    Shu, Limin
    Zhang, Chengyue
    Su, Zheng-Yuan
    Kong, Ah-Ng Tony
    [J]. BIOCHEMICAL PHARMACOLOGY, 2015, 94 (02) : 69 - 78