Impacts of fullerene C60 and virgin olive oil on cadmium-induced genotoxicity in rats

被引:15
作者
Aly, Fayza M. [1 ]
Kotb, Ahmed M. [2 ]
Haridy, Mohie A. M. [3 ]
Hammad, Seddik [4 ,5 ]
机构
[1] South Valley Univ, Fac Sci, Zool Dept, Qena 83523, Egypt
[2] Assiut Univ, Fac Vet Med, Dept Anat & Histol, Assiut 71515, Egypt
[3] South Valley Univ, Fac Vet Med, Dept Pathol & Clin Pathol, Qena 83523, Egypt
[4] South Valley Univ, Fac Vet Med, Dept Forens Med & Toxicol, Qena 83523, Egypt
[5] Mannheim Heidelberg Univ, Med Fac, Dept Med 2, Mol Hepatol Sect, D-68167 Mannheim, Germany
关键词
Fullerene C-60; Cadmium chloride; Genotoxicity; DNA damage and chromosomal aberration; ENVIRONMENTAL-POLLUTANTS; CARBON NANOTUBES; RISK-ASSESSMENT; WATER; CYTOTOXICITY; CHLORIDE; HEPATOTOXICITY; BIOMARKERS; POLLUTION; TOXICITY;
D O I
10.1016/j.scitotenv.2018.02.205
中图分类号
X [环境科学、安全科学];
学科分类号
083001 [环境科学];
摘要
Currently, cadmium is considered to be one of the major environmental pollutants. Environmentally, cadmium is released in various forms e.g. oxide, chloride and sulphide. The aim of the present study was to examine the genotoxic impact of fullerene nanoparticles C-60 (C-60) and virgin olive oil (VOO) on cadmium chloride (CdCl2)-induced genotoxicity in rats. To evaluate these effects on DNA damage and chromosomal frequency, 25 albino rats were randomly assigned to 5 groups (n = 5 per group): Group I served as a control; Group 2 received a single intraperitoneal dose of CdCl2 (35 mg/kg); Group 3 animals were treated with C-60 (4 mg/kg, orally) every other day for 20 days; Group 4 received a single intraperitoneal dose of CdCl2 (3.5 mg/kg) and an oral dose of C-60 (4 mag); and Group 5 received a single intraperitoneal dose of CdCl2 (3.5 mg,/kg) and oral doses of VOO every other day for 20 consecutive days. Genotoxic and anti-genotoxic effects of C-60 and VOO were evaluated in the liver, kidney and bone marrow using molecular and cytogenetic assays. As expected, CdCl2 and C-60 administration was associated with band number alterations in both liver and kidney; however, C-60 pretreatment recovered to approximately basal number. Surprisingly, C-60 and VOO significantly attenuated the genotoxic effects caused by CdCl2 in livers and kidneys. In bone marrow, in addition to a reduction in the chromosomal number, several chromosomal aberrations were caused by CdCl2. These chromosomal alterations were also reversed by C-60 and VOO. In conclusion, molecular and cytogenetic studies showed that C-60 and VOO exhibit anti-genotoxic agents against CdCl2-induced genotoxicity in rats. Further studies are needed to investigate the optimal conditions for potential biomedical appliaitions of these anti-genotoxic agents. (C) 2013 Elsevier B.V. All rights reserved
引用
收藏
页码:750 / 756
页数:7
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