Hepatoprotective potential of astaxanthin against 2,3,7,8-tetrachlorodibenzo-p-dioxin in cultured rat hepatocytes

被引:14
|
作者
Turkez, Hasan [1 ]
Geyikoglu, Fatime [2 ]
Yousef, Mokhtar I. [3 ]
Togar, Basak [2 ]
Gurbuz, Hasan [4 ]
Celik, Kubra [2 ]
Akbaba, Giray B. [2 ]
Polat, Zuhal [2 ]
机构
[1] Erzurum Tech Univ, Dept Mol Biol & Genet, Fac Sci, Erzurum, Turkey
[2] Ataturk Univ, Dept Biol, Fac Sci, TR-25240 Erzurum, Turkey
[3] Univ Alexandria, Dept Environm Studies, Inst Grad Studies & Res, Alexandria, Egypt
[4] Ataturk Univ, KKEF Fac Educ, Dept Biol, TR-25240 Erzurum, Turkey
关键词
TCDD; astaxanthin; cultured rat hepatocytes; cell viability; genotoxicity; oxidative status; SPRAGUE-DAWLEY RATS; DNA STRAND BREAKS; OXIDATIVE STRESS; FREE-RADICALS; TOXICITY; CAROTENOIDS; TCDD; EXTRACT; INJURY; LIVER;
D O I
10.1177/0748233712452607
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
The purpose of this study was to evaluate the effect of carotenoid astaxanthin (ASTA) on cultured primary rat hepatocytes treated with 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) on the cell viability (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide, MTT), lactate dehydrogenase (LDH) activity, 8-oxo-2-deoxyguanosine (8-OH-dG), total antioxidant capacity (TAC), and total oxidative stress (TOS) levels, and liver micronucleus rates. ASTA (2.5, 5, and 10 mu M) was added to cultures alone or simultaneously with TCDD (5 and 10 mu M) for 48h. The results of MTT and LDH assays showed that both doses of TCDD caused significant decrease in cell viability. Also, TCDD significantly increased TOS and decreased TAC level in rat hepatocytes. On the basis of increasing doses, the dioxin caused significant increase in micronucleated hepatocytes) and 8-OH-dG level as compared to control culture. The presence of ASTA with TCDD minimized its effects on primary hepatocytes cultures and DNA damages.
引用
收藏
页码:101 / 112
页数:12
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