Effects of Epigallocatechin Gallate on Tert-Butyl Hydroperoxide-Induced Mitochondrial Dysfunction in Rat Liver Mitochondria and Hepatocytes

被引:7
|
作者
Mezera, Vojtech [1 ,2 ]
Endlicher, Rene [3 ]
Kucera, Otto [1 ]
Sobotka, Ondrej [1 ]
Drahota, Zdenek [1 ]
Cervinkova, Zuzana [1 ]
机构
[1] Charles Univ Prague, Dept Physiol, Fac Med Hradec Kralove, Hradec Kralove 50038, Czech Republic
[2] Buck Inst Res Aging, Novato, CA 94945 USA
[3] Charles Univ Prague, Fac Med Hradec Kralove, Dept Anat, Hradec Kralove 50038, Czech Republic
关键词
GREEN TEA POLYPHENOL; OXIDATIVE STRESS; LIPID-PEROXIDATION; HYDROGEN-PEROXIDE; COMPLEX I; (-)-EPIGALLOCATECHIN-3-GALLATE; ANTIOXIDANT; SUPEROXIDE; DAMAGE; CYTOTOXICITY;
D O I
10.1155/2016/7573131
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Epigallocatechin gallate (EGCG) is a green tea antioxidant with adverse effects on rat liver mitochondria and hepatocytes at high doses. Here, we assessed whether low doses of EGCG would protect these systems from damage induced by tert-butyl hydroperoxide (tBHP). Rat liver mitochondria or permeabilized rat hepatocytes were pretreated with EGCG and then exposed to tBHP. Oxygen consumption, mitochondrial membrane potential (MMP), and mitochondrial retention capacity for calcium were measured. First, 50 mu M EGCGor 0.25 mM tBHP alone increased State 4 Complex I-driven respiration, thus demonstrating uncoupling effects; tBHP also inhibited State 3 ADP-stimulated respiration. Then, the coexposure to 0.25 mM tBHP and 50 mu M EGCG induced a trend of further decline in the respiratory control ratio beyond that observed upon tBHP exposure alone. EGCG had no effect on MMP and no effect, in concentrations up to 50 mu M, on mitochondrial calcium retention capacity. tBHP led to a decline in both MMP and mitochondrial retention capacity for calcium; these effects were not changed by pretreatment with EGCG. In addition, EGCG dose dependently enhanced hydrogen peroxide formation in a cell-and mitochondria-free medium. Conclusion. Moderate nontoxic doses of EGCG were not able to protect rat liver mitochondria and hepatocytes from tBHP-induced mitochondrial dysfunction.
引用
收藏
页数:8
相关论文
共 50 条
  • [41] A MECHANISM OF MITOCHONDRIAL DAMAGE INDUCED BY TERT-BUTYL HYDROPEROXIDE AND MICROSOMES INVITRO
    MATSUO, T
    KASHIWAKI, Y
    ITOO, S
    PHYSIOLOGIA PLANTARUM, 1990, 80 (02) : 226 - 232
  • [42] Bromelain prevents mouse testis from tert-butyl hydroperoxide-induced dysfunction by inhibiting apoptosis, inflammation, and cellular senscence
    Yeh, Yueh-Chiao
    Tsai, Ching-Han
    Liu, Tsun-Jui
    Lai, Hui-Chin
    Wang, Li-Chuan
    FASEB JOURNAL, 2013, 27
  • [43] Protective Effect of Caffeic Acid Derivatives on tert-Butyl Hydroperoxide-Induced Oxidative Hepato-Toxicity and Mitochondrial Dysfunction in HepG2 Cells
    Tsai, Tzung-Hsun
    Yu, Chun-Hsien
    Chang, Yu-Ping
    Lin, Yu-Ting
    Huang, Ching-Jang
    Kuo, Yueh-Hsiung
    Tsai, Po-Jung
    MOLECULES, 2017, 22 (05):
  • [44] Inhibitory effect of atractylon on tert-butyl hydroperoxide induced DNA damage and hepatic toxicity in rat hepatocytes
    Hwang, JM
    Tseng, TH
    Hsieh, YS
    Chou, FP
    Wang, CJ
    Chu, CY
    ARCHIVES OF TOXICOLOGY, 1996, 70 (10) : 640 - 644
  • [45] Effects of lovastatin on tert-butyl hydroperoxide induced cell toxicity
    Krasteva, A.
    Mitcheva, M.
    Descatoire, V.
    TOXICOLOGY LETTERS, 2005, 158 : S54 - S55
  • [46] Effect of caffeic acid on tert-butyl hydroperoxide-induced oxidative stress in U937
    Nardini, M
    Pisu, P
    Gentili, V
    Natella, F
    Di Felice, M
    Piccolella, E
    Scaccini, C
    FREE RADICAL BIOLOGY AND MEDICINE, 1998, 25 (09) : 1098 - 1105
  • [47] Protective effect of Hibiscus anthocyanins against tert-butyl hydroperoxide-induced hepatic toxicity in rats
    Wang, CJ
    Wang, JM
    Lin, WL
    Chu, CY
    Chou, FP
    Tseng, TH
    FOOD AND CHEMICAL TOXICOLOGY, 2000, 38 (05) : 411 - 416
  • [48] Baicalein protects tert-butyl hydroperoxide-induced hepatotoxicity dependent of reactive oxygen species removal
    Wang, Ya-Fang
    Tang, Zheng-Hai
    Li, Ting
    Xu, Xiao-Huang
    Chen, Xiuping
    Wang, Ying
    Wang, Yi-Tao
    Lu, Jin-Jian
    MOLECULAR MEDICINE REPORTS, 2017, 16 (06) : 8392 - 8398
  • [49] Protective effect of the coffee Diterpenes kahweol and cafestol on tert-butyl hydroperoxide-induced oxidative hepatotoxicity
    Choi, Sun Young
    Lee, Kyung Jin
    Kim, Hyung Gyun
    Han, Eun Hee
    Chung, Young Chul
    Sung, Nak Ju
    Jeongt, Hye Gwang
    BULLETIN OF THE KOREAN CHEMICAL SOCIETY, 2006, 27 (09) : 1386 - 1392
  • [50] GENDER-RELATED RESPONSE TO A TERT-BUTYL HYDROPEROXIDE-INDUCED OXIDATION IN HUMAN NEONATAL TISSUE
    LAVOIE, JC
    CHESSEX, P
    FREE RADICAL BIOLOGY AND MEDICINE, 1994, 16 (03) : 307 - 313