PMID- 20388359 OWN - NLM STAT- MEDLINE DCOM- 20100610 LR - 20201209 IS - 0253-9624 (Print) IS - 0253-9624 (Linking) VI - 44 IP - 1 DP - 2010 Jan TI - [The antagonistic action of epigallocatechin-3-gallate on microcystin LR-induced oxidative damage on hepatocytes of mice and the expression of cytochrome P450 2E1]. PG - 24-9 AB - OBJECTIVE: To evaluate the effects of antagonistic action of epigallocatechin-3-gallate (EGCG) on microcystin LR (MC-LR) induced oxidative damage on mice and the expression of cytochrome P450 2E1 (CYP2E1) which was one of phase Iota detoxification enzymes. METHODS: A total of 24 specific pathogen free (SPF) male BALB/c mice were randomly divided into four groups, including control group, MC-LR group, low concentration EGCG group, and high concentration EGCG group. Mice were sacrificed on the 15th day, body weight, and the relative organ weight, liver antioxidant enzyme level and lipid peroxidation product, liver histopathology and CYP2E1 gene and protein expression were detected and analyzed respectively. RESULTS: (1) EGCG could antagonise the liver injury which had been damaged by MC-LR. (2) The malonaldehyde (MDA) level ((2.87 +/- 0.03) nmol/mg prot) and superoxide dismutase (SOD) level ((168.18 +/- 2.86) U/mg prot) in MC-LR group were significantly different when compared with the two EGCG treatment groups (the MDA values of the low and high concentration EGCG group were (2.37 +/- 0.05) nmol/mg prot and (1.44 +/- 0.05) nmol/mg prot, F = 906.63, P < 0.01; the SOD values were (176.55 +/- 2.98) U/mg prot and (184.89 +/- 1.53) U/mg prot, F = 32.32, P < 0.01). (3) MC-LR up-regulated the mRNA and protein expression of CYP2E1 (the mRNA values of MC-LR group and control were 1.41 +/- 0.26, 0.86 +/- 0.13, t = -4.22, P = 0.003; the protein values of MC-LR group and control were 0.24 +/- 0.03, 0.12 +/- 0.02, t = -9.21, P < 0.05). EGCG down-regulated the mRNA (the values of the low and high concentration EGCG group were 1.09 +/- 0.08, 0.99 +/- 0.09, F = 9.03, P = 0.004) and protein expression (the values of the low and high concentration EGCG group were 0.21 +/- 0.03, 0.14 +/- 0.02, F = 24.76, P < 0.05) of CYP2E1 which activated by MC-LR. CONCLUSION: The up-regulation of CYP2E1 which induced by MC-LR was inhibited by EGCG intervention. EGCG might antagonize the oxidation damage of hepatocytes in a certain degree. FAU - Han, Zhi-Xia AU - Han ZX AD - Department of Environmental Hygiene, School of Military Preventive Medicine, The Third Military Medical University, Chongqing 400038, China. FAU - Yang, Lan AU - Yang L FAU - Zhang, Liang AU - Zhang L FAU - Xu, Chuan AU - Xu C FAU - Shu, Wei-Qun AU - Shu WQ LA - chi PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - China TA - Zhonghua Yu Fang Yi Xue Za Zhi JT - Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine] JID - 7904962 RN - 0 (Marine Toxins) RN - 0 (Microcystins) RN - 8R1V1STN48 (Catechin) RN - BQM438CTEL (epigallocatechin gallate) RN - EC 1.14.13.- (Cytochrome P-450 CYP2E1) RN - EQ8332842Y (cyanoginosin LR) SB - IM MH - Animals MH - Catechin/*analogs & derivatives/pharmacology MH - Cytochrome P-450 CYP2E1/*metabolism MH - Hepatocytes/*drug effects/*metabolism MH - Male MH - Marine Toxins MH - Mice MH - Mice, Inbred BALB C MH - Microcystins/adverse effects MH - Oxidative Stress/*drug effects EDAT- 2010/04/15 06:00 MHDA- 2010/06/11 06:00 CRDT- 2010/04/15 06:00 PHST- 2010/04/15 06:00 [entrez] PHST- 2010/04/15 06:00 [pubmed] PHST- 2010/06/11 06:00 [medline] PST - ppublish SO - Zhonghua Yu Fang Yi Xue Za Zhi. 2010 Jan;44(1):24-9.