Ojha A, Gupta Y K
Department of Pharmacology, All India Institute of Medical Sciences, New Delhi, India.
Department of Pharmacology, All India Institute of Medical Sciences, New Delhi, India
Hum Exp Toxicol. 2015 Apr;34(4):390-400. doi: 10.1177/0960327114537534. Epub 2014 Sep 8.
Chlorpyrifos (CPF), methyl parathion (MPT), and malathion (MLT) are among the most extensively used organophosphate (OP) pesticides in India. DNA protein cross-links (DPC) and DNA strand breaks are toxic lesions associated with the mechanism(s) of toxicity of carcinogenic compounds. In the present study, we examined the hypothesis that individual and interactive genotoxic effects of CPF, MPT, and MLT are involved in the formation of DPC and DNA strand break. The DNA strand break was measured by comet assay and expressed as DNA damage index, while DPC estimation was carried out by fluorescence emission assay. The results showed that exposure of rat lymphocytes with CPF, MPT, and MLT caused significantly marked increase in DNA damage and DPC formation in time-dependent manner. MPT caused the highest damage, and these pesticides do not potentiate the toxicity of each other.
毒死蜱(CPF)、甲基对硫磷(MPT)和马拉硫磷(MLT)是印度使用最广泛的有机磷(OP)农药。DNA-蛋白质交联(DPC)和DNA链断裂是与致癌化合物毒性机制相关的毒性损伤。在本研究中,我们检验了以下假设:CPF、MPT和MLT的个体和联合遗传毒性效应参与了DPC和DNA链断裂的形成。通过彗星试验测量DNA链断裂,并将其表示为DNA损伤指数,而DPC的估计则通过荧光发射试验进行。结果表明,用CPF、MPT和MLT处理大鼠淋巴细胞会导致DNA损伤和DPC形成随时间显著增加。MPT造成的损伤最大,并且这些农药之间不会相互增强毒性。