ISSN Print: 2381-1420  ISSN Online: 2381-1447
AASCIT Journal of Medicine  
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Structural Characterization of the Kidney Following Lactational Lead Intoxication in Sprague Dawley Rats
AASCIT Journal of Medicine
Vol.4 , No. 2, Publication Date: May 16, 2018, Page: 25-31
768 Views Since May 16, 2018, 340 Downloads Since May 16, 2018
 
 
Authors
 
[1]    

Odukoya Samson Ayodeji, Department of Anatomy and Cell Biology, Faculty of Basic Medical Sciences, Obafemi Awolowo University, Ile-Ife, Osun State, Nigeria.

[2]    

Olatunji Olanrewaju James, Department of Anatomy, Faculty of Basic Medical Sciences, College of Health Sciences, Bowen University, Iwo Osun State, Nigeria.

[3]    

Komolafe Omobola Aderibigbe, Department of Anatomy and Cell Biology, Faculty of Basic Medical Sciences, Obafemi Awolowo University, Ile-Ife, Osun State, Nigeria.

[4]    

Saka Olusola Stephen, Department of Anatomy and Cell Biology, Faculty of Basic Medical Sciences, Obafemi Awolowo University, Ile-Ife, Osun State, Nigeria.

[5]    

Odukoya Abimbola Opeyemi, Obafemi Awolowo Teaching Hospital Complex, Ile Ife, Osun-State, Nigeria.

 
Abstract
 

This study was designed to examine the effect oflactational lead intoxication in the kidney of Sprague-Dawley rats. 12 female rats were used in the experiment. These rats mated with male rats to reproduce 23 offspring for the analysis of lactational lead intoxication. The offspring were divided into four groups. Groups B, C and D were administered 10 mg/dL, 30 mg/dL and 70 mg/dL of lead acetate respectively while group A was control. The animal was firstly sedated using a chloroform-damped cotton wool in a vacuum (air-tight chamber). The sedated animal was weighed on a weighing balance and figure recorded. The animal was then perfused to clear blood from the organs before the organs were harvested. The kidneys were removed, weighed and fixed by immersion in 4% formal saline for further histological processing. The result showed the total body weight appeared to be significantly (p<0.05) lower in groups B, C and D when compared to the control group (29.00±2.31g) and is significantly (p < 0.05) higher in groups B and C when compared to the control. Also, total body length, right and left kidneys showed a significant (p<0.05) increased in group B when compared to the control group in both male and female. Abnormalities in the functional components of the kidney were observed with a rise in the administered dose, with the condition being most severe in the group treated with 70mg administration. It is concluded that high levels of lactational lead is very toxic to rat pups causing histoarchitectural pathologies in the kidney.


Keywords
 

Lactational, Lead, Intoxication, Kidney


Reference
 
[01]    

Flora, S. J. S., G. J. S. Flora and G. Saxena. Environmental Occurrence, Health Effects and Management of Lead Poisoning. In: Casas, S. B. and J. Sordo (Eds.), Lead: Chemistry, Analytical Aspects, Environmental Impact and Health Effects. Elsevier, the Netherlands 2006, pp: 158-228.

[02]    

Hernberg S. "Lead poisoning in a historical perspective". American journal of industrial medicine 2000; 38 (3): 244–54.

[03]    

Garaza, A., R. Vega and E. Soto. Cellular mechanisms of lead neurotoxicity. Med. Sci. Monitor. 2006; 12 (3): 57-65.

[04]    

Diamond, G. L. Risk Assessment of Nephrotoxic Metals. In: Tarloff, J. and L. Lash (Eds.), the Toxicology of the Kidney. CRC Press, London 2005; pp: 1099-1132.

[05]    

Aziz, F. M., I. M. Maulood and M. A. H. Chawsheen. Effects of melatonin, vitamin C and E alone or in combination on lead-induced injury in liver and kidney organs of rats. IOSR J. Pharm. 2012; 2 (5): 13-18.

[06]    

El-Neweshy, M. S. and Y. S. El-Sayed. Exp. Toxicol. Pathol. 2011; 63 (3): 221-227. Influence of vitamin C supplementation on lead-induced histopathological alterations in male rats.

[07]    

Payal, B., H. P. Kaur and D. V. Rai. New insight into the effects of lead modulation on antioxidant defense mechanism and trace element concentration in rat bone. Interdiscip. Toxicol. 2009; 2 (1): 18-23.

[08]    

Bomfim, K. M. A, C. A. B Garcia, F. P. Reis, J. A. V. Palmeira, R. Scher and D. E. Lucca. Absorption levels and morphological features of fetal organs in wistar rats treated with lead acetate. Int. J. Morphol. 2012; 30 (1): 119-124.

[09]    

Garu, U., R. Sharma and I. Barber, 2011. Effect of lead toxicity on developing testis of mice. Int. J. Pharma. Sci. Res. 2011; 2 (9): 2403-2407.

[10]    

Moussa, S. A. and S. A. Bashandy. Biophysical and biochemical changes in the blood of rats exposed to lead toxicity. Rom. J. Biophys. 2008; 18 (2): 123-133.

[11]    

Diamond GL. Risk assessment of nephrotoxic metals. In: Tarloff J, Lash L, eds. The toxicology of the kidney. London: CRC Press 2005; 1099-1132.

[12]    

Goyer RA. Lead toxicity: Current concerns. Environ. Health Perspect. 1993; 100: 177-187.

[13]    

Loghman-Adham M. Renal effects of environmental and occupational lead exposure Environ. Health Perspect. 1997; 105: 928-939.

[14]    

Biagini G, Caudarelia R, Vangelista. Renal morphological and functional modification in chronic lead poisoning. In: Brown SS, ed. Clinical chemistry and chemical toxicology of metals. Elsevier/North- Holland Biomedical Press 1977; pp. 123-126.

[15]    

Cramer K, GoyerRA, Jagenburg R. Renal ultrastructure, renal function and parameters of lead toxicity in workers with different periods of lead exposure. Br. J. Ind. Med. 1974; 31: 113-127.

[16]    

Aviv A, John E, Bernstein J. Lead intoxication during development: Its late effect on kidney function and blood pressure. Kidney Int. 1980; 17: 430-437.

[17]    

Dieter MP, Matthews HB, Jeffcoat RA. Comparison of lead bioavailability in F344 rats fed lead acetate, lead oxide, lead sulfide, or lead ore concentrate from Skagway, Alaska. J. Toxicol. Environ. Health 1993; 39: 79-93.

[18]    

Khalil-Manesh F, Gonick HC, Cohen AH. Experimental model of lead nephropathy. I. Continuous high-dose lead administration. Kidney Int. 1992; 41: 1192-1203.

[19]    

Murakami M, Kawamura R, Nishii S. Early appearance and localization of intranuclear inclusions in the segments of renal proximal tubules of rats following ingestion of lead. Br. J. Exp. Pathol. 1983; 64: 144-155.

[20]    

Khalil-Manesh F, Tartaglia-Erler J and Gonick HC. Experimental model of lead nephropathy. IV. Correlation between renal functional changes and haematological indices of lead toxicity. J Trace Elem Electrolytes Health Dis. 1994; 8 (1): 13-19.

[21]    

Restek-Samarzija N and Momcilovic B. [Late changes in renal function after lead poisoning and chelation therapy-Article in Czech]. ArhHigRadaToksikol. 1992; 43 (4): 321- 8.

[22]    

Nabil MI, Esam AE, Hossam SE and Abdel-Mobdy YE. Effect of lead acetate toxicity on experimental male albino rats. Asian Pac J Trop Biomed. 2012; 2 (1): 41-46.

[23]    

Hwang DF and Wang LC. Effect of taurine on toxicity of cadmium in rats. Toxicology. 2001; 167: 173-180.

[24]    

Wright LS, Kornguth SE, Oberley DT and Siegel LF. Effect of lead on Glutathione S-Transferase Expression in Rat kidney: a dose response study. Toxicological sciences. 1998; 46: 254-259.

[25]    

Pounds JG, Long GJ and Rosen JF. Cellular and molecular toxicity of lead in bone. Environ Health Perspect. 1991; 91: 17–32.

[26]    

Fowler BA, Kimmel CA, Wood JS, Ernest EM and Grant LD. Chronic low-level lead toxicity in rat; an integrate assessment of long-toxicity with special reference to the kidney. Toxicol. Appl. Phmcol. 1980; 180: 56-59.

[27]    

Loghman-Adham M. Renal effects of environmental and occupational lead exposure. Environ Health Perspect. 1997; 105 (9): 928-938.

[28]    

Perneger TV, Whelton PK and Klag MJ. "Risk of Kidney Failure Associated with the Use of Acetaminophen, Aspirin, and NonsteroidalAntiinflammatory Drugs". New England Journal of Medicine 1994; 331 (25).

[29]    

Landrigan PJ, Sonawane B, Mattison D, McCally M and Garg A. Chemical contaminants in breast milk and their impacts on children’s health: an overview. Environ Health Perspect. 2002; 110: A313–A315.





 
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