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杨敬华, 徐兆发, 徐斌, 贺安宁. 镉致大鼠肾脏毒性机制研究[J]. 中国公共卫生, 2007, 23(7): 887-888. DOI: 10.11847/zgggws2007-23-07-62
引用本文: 杨敬华, 徐兆发, 徐斌, 贺安宁. 镉致大鼠肾脏毒性机制研究[J]. 中国公共卫生, 2007, 23(7): 887-888. DOI: 10.11847/zgggws2007-23-07-62
YANG Jing-hua, XU Zhao-fa, XU Bin, . Study on mechanism of toxicity induced by cadmium in kidney[J]. Chinese Journal of Public Health, 2007, 23(7): 887-888. DOI: 10.11847/zgggws2007-23-07-62
Citation: YANG Jing-hua, XU Zhao-fa, XU Bin, . Study on mechanism of toxicity induced by cadmium in kidney[J]. Chinese Journal of Public Health, 2007, 23(7): 887-888. DOI: 10.11847/zgggws2007-23-07-62

镉致大鼠肾脏毒性机制研究

Study on mechanism of toxicity induced by cadmium in kidney

  • 摘要: 目的 研究镉对肾脏产生的毒性作用,并初步探讨镉的肾脏毒性机制。方法 低、中、高剂量染镉组大鼠分别皮下注射3,5,7μmol CdCl2/(kg·bw)6周。测定尿镉、蛋白含量和尿N-乙酰-β-D氨基葡萄糖苷酶(NAG)、碱性磷酸酶(ALP)、乳酸脱氢酶(LDH)活性,测定肝脏和肾皮质丙二醛(MDA)和谷胱甘肽(GSH)含量。结果 尿蛋白含量和尿NAG、ALP、LDH活性以及肝、肾皮质MDA和GSH含量随染镉剂量增加而升高。中剂量染镉组尿蛋白含量和尿NAG、LDH活性以及肾皮质MDA、GSH含量显著高于对照组和低剂量染镉组。高剂量染镉组尿蛋白含量、ALP活性、肝和肾皮质MDA显著高于对照组和低中剂量染镉组。且尿镉、蛋白含量、尿NAG、ALP、LDH活性与肾皮质MDA含量呈显著正相关。结论 镉生物学效应随染毒剂量增加而增强,CdCl25μmol/(kg.bw)对肾脏产生一定损伤作用,CdCl27μmol/(kg.bw)时肾脏损伤加重。镉的肾毒性机制与其氧化损伤作用有关。

     

    Abstract: Objective To study toxic effects of cadmium(Cd)on the kidney,and discuss the mechanism of to xicity induced by Cd in kidney.Methods Three Cd groups rats were injected with CdCl2 3,5 and 7 μmol/kg per day for 6 weeks,respectively.Urinary Cd,protein contents and N-acetyl-B-D-glucosaminidase(NAG),alkaline phosphalase(ALP),lactic dehy drogenase(LDH)were measured.Malondialdehyde(MDA),glutathione(GSH)contents in the liver and renal cortex were determined.Results Urinary Cd,protein contents,NAG,A LP,LDH activities and MDA,GSH contents in the liver and renal cortex increased with Cd dose increasing.Urinary protein contents,NAG,LDH activities and MDA,GSH contents in the renal cortex of middle-dose Cd group were higher significantly than those of control and low-dose Cd group.To high-dose Cd group,ur inary protein contents,ALP activities and MDA contents in the liver and renal cortex were higher significantly than that of control,low-and middle-dose Cd group.Urinary Cd,protein contents and NAG,ALP,LDH activities were corr elated positively with MDA contents in the renal cortex.Conclusion The biological effect of Cd enhanced with Cd dose increasing.CdCl2 5μmol/(kg·bw)could induce renal injuries,and CdCl2 7μmol/(kg·bw)could induce more evident injuries.Furthermore,the mechanism was correlated positively with oxidative injuries caused by Cd.

     

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