Influence of resveratrol on oxidative damage in genomic DNA and apoptosis induced by cisplatin

被引:62
作者
Attia, Sabry M. [1 ]
机构
[1] King Saud Univ, Coll Pharm, Dept Pharmacol, Riyadh 11451, Saudi Arabia
关键词
Cisplatin; Resveratrol; Oxidative DNA damage; Apoptosis; Somatic cells; Germ cells; MOUSE BONE-MARROW; PERIPHERAL-BLOOD LYMPHOCYTES; IN-VIVO EVIDENCE; INDUCED NEPHROTOXICITY; CHROMOSOMAL DAMAGE; TRANS-RESVERATROL; CHEMOTHERAPY; CANCER; CELLS; ASSAY;
D O I
10.1016/j.mrgentox.2011.10.008
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Cisplatin is a potent chemotherapeutic agent that has gained widespread use against various malignant tumours in a variety of human malignancies. Like other chemotherapeutic agents, cisplatin is genotoxic and apoptogenic in non-tumour cells and the formation of reactive oxygen species appears robe responsible for these toxicities. The anti-genotoxic and anti-apoptotic effects of resveratrol, a polyphenol found in numerous plant species, against cisplatin-induced genotoxicity and apoptosis in vivo were evaluated by use of standard techniques in somatic and germinal cells of mice. Pre-treatment of mice with resveratrol significantly reduced cisplatin-induced genotoxicity and apoptosis and effectively suppressed the apoptotic signalling triggered by cisplatin. The protective effect of resveratrol was found to be stronger at the higher dose, indicating the dose-dependent effect of resveratrol. Cisplatin induced marked biochemical alterations characteristic of oxidative DNA stress. Prior administration of resveratrol before the cisplatin challenge ameliorated these biochemical markers. In conclusion, this study provides evidence for the first time that resveratrol has a protective role in the abatement of cisplatin-induced genotoxicity and apoptosis in somatic and germinal cells of mice. This activity resides, at least in part, in its radical scavenger activity. Therefore, resveratrol can be a promising chemoprotective agent to avert secondary malignancies and abnormal reproductive outcomes in cured cancer patients exposed to cisplatin, without diminishing its anti-neoplastic activity. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:22 / 31
页数:10
相关论文
共 51 条
[1]
Adler I.-D., 1984, MUTAGENICITY TESTING, P275
[2]
CLASTOGENIC EFFECTS OF CIS-DIAMMINEDICHLOROPLATINUM .1. INDUCTION OF CHROMOSOMAL-ABERRATIONS IN SOMATIC AND GERMINAL CELLS OF MICE [J].
ADLER, ID ;
ELTARRAS, A .
MUTATION RESEARCH, 1989, 211 (01) :131-137
[3]
Aggarwal BB, 2004, ANTICANCER RES, V24, P2783
[4]
ANDERSON ME, 1985, METHOD ENZYMOL, V113, P548
[5]
Assessment of genomic instability in normal and diabetic rats treated with metformin [J].
Attia, S. M. ;
Helal, G. K. ;
Alhaider, A. A. .
CHEMICO-BIOLOGICAL INTERACTIONS, 2009, 180 (02) :296-304
[6]
Attia S.M., 2008, SPJ, V16, P120
[7]
Abatement by naringin of lomefloxacin-induced genomic instability in mice [J].
Attia, Sabry M. .
MUTAGENESIS, 2008, 23 (06) :515-521
[8]
The genotoxic and cytotoxic effects of nicotine in the mouse bone marrow [J].
Attia, Sabry M. .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2007, 632 (1-2) :29-36
[9]
Proanthocyanidins produce significant attenuation of doxorubicin-induced mutagenicity via suppression of oxidative stress [J].
Attia, Sabry M. ;
Bakheet, Saleh A. ;
Al-Rasheed, Nouf M. .
OXIDATIVE MEDICINE AND CELLULAR LONGEVITY, 2010, 3 (06) :404-413
[10]
The impact of quercetin on cisplatin-induced clastogenesis and apoptosis in murine marrow cells [J].
Attia, Sabry M. .
MUTAGENESIS, 2010, 25 (03) :281-288