Teratogenic effects of lead acetate on kidney.

BACKGROUND Lead remains a considerable occupational and public health problem, which is known to cause a number of adverse effects in both men and women. Conflicting reports have appeared on lead induced nephrotoxicity in experimental studies in the past. There is hardly any work on its teratogenic effects on kidney. Present study was therefore designed to investigate the effects of lead acetate on developing kidney. METHODS Twelve mice were used as experimental model and were divided into two groups of six animals each; group A served as control group and B was used as an experimental group. Lead acetate (10 mg/kg) dissolved in 0.02 ml of distilled water was administered as a single daily dose orally to group B whereas weight related amount of distilled water was given to group A for the entire period of experiment. On 18th day of gestation foetuses were dissected free of uterine wall under the dissecting microscope and were sacrificed; kidneys were removed and fixed in 10% formalin, dehydrated in ascending grades of alcohol, cleared in xylene and infiltrated with filtered paraffin. The paraffin blocks were made and five micron thin sections were obtained using a rotary microtome. The sections were stained with Hematoxylin and eosin and, PAS; these were examined under light microscope. RESULTS Significant decrease in cortical thickness was observed which varied from 578.61 +/- 1.4 microm in group A to 515.6 +/- 5 microm in group B (p < 0.001). Diameter of renal corpuscles varied from 57.7 +/- 0.07 microm in group A to 50.5 +/- 0.07 microm in group B (p < 0.001). Moderate cortical tubular atrophy showing thickening of endothelial basement membrane in glomeruli, desquamated epithelium with degenerated nuclei in proximal and distal tubules were observed in group B in contrast to group A. CONCLUSION The results of the investigation indicated that lead acetate administration to the dams produced deleterious effects on the developing kidney in mice.

[1]  G. Gonzales,et al.  Lepidium meyenii (Maca) reversed the lead acetate induced -- damage on reproductive function in male rats. , 2006, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

[2]  Feng-sen Xu,et al.  [Effects of lead exposure to rat placenta and pups during different gestation periods]. , 2006, Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine].

[3]  N. Naha,et al.  Toxic effect of lead on human spermatozoa: A study among pigment factory workers , 2005 .

[4]  S. Suzuki,et al.  Development of gender differences in DBA/2Cr mouse kidney morphology during maturation. , 2005, The Journal of veterinary medical science.

[5]  M. Hassouna,et al.  Amelioration of lead toxicity on rat liver with Vitamin C and silymarin supplements. , 2005, Toxicology.

[6]  U. R. Acharya,et al.  Protective action of vitamins on the spermatogenesis in lead-treated Swiss mice. , 2004, Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements.

[7]  T. Michalska,et al.  Detection of lead-induced oxidative stress in the rat epididymis by chemiluminescence. , 2004, Chemosphere.

[8]  A. Poma,et al.  Lead acetate genotoxicity on human melanoma cells in vitro , 2003, Melanoma research.

[9]  A. Hakeem,et al.  Blood lead levels during pregnancy and pregnancy outcome in Karachi women. , 2003, JPMA. The Journal of the Pakistan Medical Association.

[10]  U. R. Acharya,et al.  Lead acetate induced cytotoxicity in male germinal cells of Swiss mice. , 2003, Industrial health.

[11]  J. López-Novoa Role of Reactive Oxygen Species in Renal Function and Diseases , 2002 .

[12]  M. Goldberg,et al.  Clinical evaluation and management of lead-exposed construction workers. , 2000, American journal of industrial medicine.

[13]  N. Vaziri,et al.  Lead-induced hypertension: interplay of nitric oxide and reactive oxygen species. , 1997, Hypertension.

[14]  D. K. Saxena,et al.  Lead-induced changes in ovarian follicular development and maturation in mice. , 1997, Journal of toxicology and environmental health.

[15]  A. Vyskočil,et al.  Effect of prenatal and postnatal exposure to lead on kidney function in male and female rats , 1995, Journal of applied toxicology : JAT.

[16]  A. Chowdhury,et al.  Toxic effect of lead on the testes of rat. , 1983, Biomedica biochimica acta.

[17]  B. Fowler,et al.  Effects of concurrent administration of lead, cadmium, and arsenic in the rat , 1977, Environmental health perspectives.