Ameliorative Influence of Green Tea Extract on Copper Nanoparticle-Induced Hepatotoxicity in Rats

被引:37
|
作者
Ibrahim, Marwa A. [1 ]
Khalaf, A. A. [2 ]
Galal, Mona K. [1 ]
Ogaly, Hanan A. [1 ]
Hassan, Azza H. M. [3 ]
机构
[1] Cairo Univ, Fac Vet Med, Dept Biochem & Chem Nutr, Giza, Egypt
[2] Cairo Univ, Fac Vet Med, Dept Forens Med & Toxicol, Giza, Egypt
[3] Cairo Univ, Fac Vet Med, Dept Parasitol, Giza, Egypt
来源
关键词
CNPs; Liver; Apoptosis; Oxidative stress; Green tea extract; Rats; OXIDATIVE STRESS; NANO-COPPER; OXIDE NANOPARTICLES; LIPID-PEROXIDATION; INDUCED APOPTOSIS; AIR-POLLUTANTS; CELL-DEATH; MECHANISMS; DAMAGE; LIVER;
D O I
10.1186/s11671-015-1068-z
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The potential toxicity of copper nanoparticles (CNPs) to the human health and environment remains a critical issue. In the present study, we investigated the protective influence of an aqueous extract of green tea leaves (GTE) against CNPs-induced (20-30 nm) hepatotoxicity. Four different groups of rats were used: group I was the control, group II received CNPs (40 mg/kg BW), group III received CNPs plus GTE, and group IV received GTE alone. We highlighted the hepatoprotective effect of GTE against CNPs toxicity through monitoring the alteration of liver enzyme activity, antioxidant defense mechanism, histopathological alterations, and DNA damage evaluation. The rats that were given CNPs only had a highly significant elevation in liver enzymes, alteration in oxidant-antioxidant balance, and severe pathological changes. In addition, we detected a significant elevation of DNA fragmentation percentage, marked DNA laddering, and significance over expression of both caspase-3 and Bax proteins. The findings for group III clarify the efficacy of GTE as a hepatoprotectant on CNPs through improving the liver enzyme activity, antioxidant status, as well as suppressing DNA fragmentation and the expression of the caspase-3 and Bax proteins. In conclusion, GTE was proved to be a potential hepatoprotective additive as it significantly ameliorates the hepatotoxicity and apoptosis induced by CNPs.
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收藏
页数:9
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