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.
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页数:8
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