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首页> 外文期刊>Biological Trace Element Research >Hematotoxicity and Genotoxicity of Mercuric Chloride Following Subchronic Exposure Through Drinking Water in Male Rats
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Hematotoxicity and Genotoxicity of Mercuric Chloride Following Subchronic Exposure Through Drinking Water in Male Rats

机译:慢性饮水对雄性大鼠的氯化汞的血液毒性和遗传毒性

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摘要

Erythrocytes are a convenient model to understand the subsequent oxidative deterioration of biological macromolecules in metal toxicities. The present study examined the variation of hematoxic and genotoxic parameters following subchronic exposure of mercuric chloride via drinking water and their possible association with oxidative stress. Male rats were exposed to 50 ppm (HG1) and 100 ppm (HG2) of mercuric chloride daily for 90 days. A significant dose-dependent decrease was observed in red blood cell count, hemoglobin, hematocrit, and mean cell hemoglobin concentration in treated groups (HG1 and HG2) compared with controls. A significant dose-dependent increase was observed in lipid peroxidation; therefore, a significant variation was found in the antioxidant enzyme activities, such as superoxide dismutase, catalase, and glutathione peroxidase. Interestingly, mercuric chloride treatment showed a significant dose-dependent increase in frequency of total chromosomal aberration and in percentage of aberrant bone marrow metaphase of treated groups (p < 0.01). The oxidative stress induced by mercury treatment may be the major cause for chromosomal aberration as free radicals lead to DNA damage. These data will be useful in screening the antioxidant activities of natural products, which may be specific to the bone marrow tissue.
机译:红细胞是了解生物大分子随后在金属毒性中氧化降解的便捷模型。本研究研究了通过饮用水亚慢性暴露于氯化汞后血液毒性和遗传毒性参数的变化及其可能与氧化应激的关系。雄性大鼠每天暴露于50 ppm(HG1)和100 ppm(HG2)的氯化汞中90天。与对照组相比,治疗组(HG1和HG2)的红细胞计数,血红蛋白,血细胞比容和平均细胞血红蛋白浓度均出现明显的剂量依赖性降低。在脂质过氧化中观察到明显的剂量依赖性增加;因此,发现抗氧化酶的活性发生了显着变化,例如超氧化物歧化酶,过氧化氢酶和谷胱甘肽过氧化物酶。有趣的是,氯化汞治疗的总染色体畸变频率和治疗组异常骨髓中期百分比显着呈剂量依赖性增加(p <0.01)。汞处理引起的氧化应激可能是染色体畸变的主要原因,因为自由基会导致DNA损伤。这些数据将有助于筛选天然产物的抗氧化活性,而天然产物可能是骨髓组织特有的。

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