2007•Chinese Journal of Public HealthRequires access

Study on mechanism of toxicity induced by cadmium in kidney

Bin Xu

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Abstract

Objective To study toxic effects of cadmium(Cd) on the kidney,and discuss the mechanism of toxicity 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-β-D-glucosaminidase(NAG),alkaline phosphalase(ALP),lactic dehydrogenase(LDH) were measured.Malondialdehyde(MDA),glutathione(GSH) contents in the liver and renal cortex were determined.Results Urinary Cd,protein contents,NAG,ALP,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,urinary 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 correlated positively with MDA contents in the renal cortex.Conclusion The biological effect of Cd enhanced with Cd dose increasing.CdCl2 5 μmol /(kg·bw)could induce renal injuries,and CdCl2 7 μmol /(kg·bw)could induce more evident injuries.Furthermore,the mechanism was correlated positively with oxidative injuries caused by Cd.

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Objective To study toxic effects of cadmium(Cd) on the kidney,and discuss the mechanism of toxicity 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-β-D-glucosaminidase(NAG),alkaline phosphalase(ALP),lactic dehydrogenase(LDH) were measured.Malondialdehyde(MDA),glutathione(GSH) contents in the liver and renal cortex were determined.Results Urinary Cd,protein contents,NAG,ALP,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,urinary 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 correlated positively with MDA contents in the renal cortex.Conclusion The biological effect of Cd enhanced with Cd dose increasing.CdCl2 5 μmol /(kg·bw)could induce renal injuries,and CdCl2 7 μmol /(kg·bw)could induce more evident injuries.Furthermore,the mechanism was correlated positively with oxidative injuries caused by Cd.

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Available abstract

Objective To study toxic effects of cadmium(Cd) on the kidney,and discuss the mechanism of toxicity 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-β-D-glucosaminidase(NAG),alkaline phosphalase(ALP),lactic dehydrogenase(LDH) were measured.Malondialdehyde(MDA),glutathione(GSH) contents in the liver and renal cortex were determined.Results Urinary Cd,protein contents,NAG,ALP,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,urinary 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 correlated positively with MDA contents in the renal cortex.Conclusion The biological effect of Cd enhanced with Cd dose increasing.CdCl2 5 μmol /(kg·bw)could induce renal injuries,and CdCl2 7 μmol /(kg·bw)could induce more evident injuries.Furthermore,the mechanism was correlated positively with oxidative injuries caused by Cd.

Key concepts: Renal cortex, Malondialdehyde, Toxicity, Kidney, Glutathione, Cadmium, Chemistry, Endocrinology

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