Enzymatic toxicity induced by lead acetate and its possible reversal by

Authors

  • Durgesh Nandini Sharma Endocrinology and Physiology Unit, School of Studies in Zoology and Biotechnology, Vikram University, Ujjain (M.P.) 456010
  • Lata Bhattacharya Endocrinology and Physiology Unit, School of Studies in Zoology and Biotechnology, Vikram University, Ujjain (M.P.) 456010

DOI:

https://doi.org/10.7439/ijbr.v6i11.2267

Abstract

Objective: An important part of male infertility of unknown etiology may be attributed to various environmental and occupational exposures to toxic substances, such as lead. Lead is the known environmental contaminant adversely affecting the male reproductive system in human and experimental animals. The cytotoxic effects of lead on male reproductive system involve the production of reactive oxygen species (ROS) and oxidative damage in tissue. The higher quantities of ROS in testicular tissue detrimentally affected enzymatic activities so as to produce verities of biochemical abnormalities and finally reduced sperm count. Methods: Adult male mice were divided into three groups: control, treated with lead acetated (1.25 mg/kg/day) and recovery group lead acetated (1.25 mg/kg/day) with vitamin E (2 mg/kg/day). Treatments were administered by daily gavage for 45 days. After treatment testis and epididymal weights were recorded and testis was used for the biochemical analysis (acid phosphatase (ACPase), alkaline phosphatase (ALKPase), and glutathione (GSH) and epididymal was used to count sperm. Results: Administration of lead acetate at a dose of 1.25mg/kg body weight for 45 days decreased the activities of all above parameters. Lead exposure resulted in oxidative stress and this was well extrapolated from the increase in lipid peroxidation products (LPP). Coadministration of vitamin E (2 mg/kg/day) with lead acetate restored all the parameters cited above to near the control values. Conclusions: This concludes that vitamin E has beneficial effects against lead acetate induced enzymatic toxicity in testicular tissue of mice.

Downloads

Download data is not yet available.

Author Biography

  • Durgesh Nandini Sharma, Endocrinology and Physiology Unit, School of Studies in Zoology and Biotechnology, Vikram University, Ujjain (M.P.) 456010

    ASSIT. PROFESSOR school of studies in zoology and biotechnology, vikram university, ujjain

References

Castellini C, Mourvaki E, Sartini B, Cardinali R, Moretti E, Collodel G, et al. In vitro toxic effects of metal compounds on kinetic traits and ultrastructure of rabbit spermatozoa. Reprod. Toxicol, 2009, 27; 46-54.

Meeker JD, Godfrey-Bailey L, HauserR. Relationships between serum hormone levels and semen quality among men from an infertility clinic. J. Androl, 2007, 28; 397-406.

Fisher IJ, Pain DJ, ThomasVG. A review of lead poisoning from ammunition sources in terrestrial birds. J. Biol. Conser, 2006, 131;421-432.

Patra RC, Rautray AK, Swarup D. Oxidative stress in lead and cadmium toxicity and its amelioration, Veterinary Medicine International, 2011 ,11: 1-9.

Ruff HA, Markowitz ME, Bijur PE, Rosen JF. Relationships among blood lead levels, iron deficiency, and cognitive development in two-year-old children, Environmental Health Perspectives, 1996, 104(2): 180-185.

Sallmen M. (2001). Exposure to lead and male fertility. Int J Occup Med Environ Health, 2001, 14: 219-222.

Chowdhury AR. s Recent advances in heavy metals induced effect on male reproductive function- A retrospective, Al Ameen Journal of Medical Sciences, 2009, 2(2): 37-42.

Ait Hamadouche N, Slimani M, Merad-Boudia B, Zaoui C.Reproductive toxicity of lead acetate in adult male rats, American Journal of Scientific Research, 2009, 1(3): 38-50.

El-Tohamy MM, El-Nattat WS. Effect of antioxidant on lead-induced oxidative damage and reproductive dysfunction in male rabbits, Journal of American Science, 2010, 6(11): 613-622.

Biswas NM, Ghosh PK. Effect of lead on male gonadal activity in Albino Rats. Kathmandu Uni Med J, 2004; 2(1):43

Liu H, Niu R, Wang J, He Y, Wang J, China S. Changes caused by fluoride and lead in energy metabolic enzyme activities in the reproductive system of male offspring rats, Research Report on Fluoride, 2008, 41(3): 184-191.

Lavitschka R, Oliveira C, Mascara D, Farial P, Bincoletto C, Esposito E. In vitro cytotoxicity and antioxidant activity of Agaricus subrufescens extracts. African Journal of Biotechnology, 2007, 6(9):1144-1150.

Timbrell JA. Introduction to Toxicology. 2nd ed., London: Taylor and Francis, 1995.

Mahaffey KR, McKinney J, Reigart JR. Lead and Compounds. In: Environmental toxicants : Human Exposures and their health effects, 2/e. Morton lippmann. John Wiley and Sons Inc., 2000, pp. 481-521.

Adonoylo VN, Oteiza PL. Lead intoxication: Antioxidant defenses and oxidative damage in rat brain. Toxicology, 1999, 15: 135(2-3): 77-85.

Gurer H, Ozygunes H, Saygin E, Erca IN. Antioxidant effect of taurin against lead

Chow CK. Vitamin E and oxidative stress. Free Radic Biol Med, 1991, 11(2): 215-32.

Brigelius

Jones DP, Kagan VE, Aust SD, Reed DJ, Omaye ST. Impact of nutrients on cellular lipid peroxidation and antioxidant defense system. Fundam. Appl. Toxicol. 1995, 26: 1-7.

Kalender Y, Uzunhisarcikli M, Ogutcu A, Acikgoz F, Kalender S. Effects of diazinon on pseudocholinesterase activity and haematological indices in rats: the protective role of Vitamin E. Environ. Toxicol. Pharmacol, 2006, 22: 46

El-Tohamy MM, El-Nattat WS. Effect of antioxidant on lead-induced oxidative damage andreproductive dysfunction in male rabbits, Journal of American Science, 2010, 6(11): 613-622.

Sharm DN. Antienzymatic action of lead acetate and its possible reversal by antioxidant in testicular tissue of swiss albino mice during pubertal phase of life. Int. J. Appli. Bio. Pharma. Tech., 2014, 5: 282-287.

Bessey OA, Lowry OH, Brick MJ. A method for rapid determination of acid and alkaline phosphatases in 5 cu mm of serum. J. Biol. Chem. 1946; 164-321.

Grunert RR, Philips PH. A modification of nitroprusside method of analysis for glutathione. Arch. Biochem. 1951; 30: 217-225.

Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxidation in animal tissue by TBA reaction. Analt. Biochem. 1979; 95: 351-358.

Hollarden A, Fredrick JDC. Chemical mutagens: principal and methods for their detection, 1978, vol. 5 Plenum press; New York.

Wyrobek AJ, Bruce WR. Chemical induction of sperm abnormalities in mice. Proc. Natl. Acad. Sci. USA , 1975, 72(1): 4425-4429.

Gad SC, Weil CS. Statistics of toxicology In: Hayes AE, editor, Principals and methods of toxicology. 2nd ed. New York: Raven Press, 1989 p. 450.

Acharya UR, Das SS, Mishra M. Role of vitamin C and E on sperm abnormality and sperm count in Cd treated swiss mice. Cytologia, 2002, 67: 47-52.

Wyrober AJ. Bruce WR. The induction of sperm shape abnormalities in mice and human. Chem. Mutagen. 1987, 5: 275-285.

Wyrober AJ, Gordon LA, Burkhart JG, Francis MW, Kapp JR, Letz G,et al. An evaluation of the mouse sperm morphology test and other sperm tests n nonhuman mammals. A report of the US Environmental Protection Agency Gene- Tox Program. Mutat. Res. 1983, 115: 1-72.

Hsu PS, Liu MY, Hsu CC, Chen LY, Guo YL. Effects of vitamin E and / or C on reactive oxygen species- related lead toxicity in rat sperm. Toxicology, 1998, 128 (3): 169-179.

Bench G, Corzett MH, Martinelli R, Balhorn R. Cadmium concentration in the testes, sperm and spermatids of mice subjected to long-term cadmium chloride exposure. Cytometry, 1999, 35: 30-36.

Kappus H. Lipid peroxidation mechanisms, analysis, enzymology and biological relevance. In Sies H editor. Oxidative stress. Academic press; Lodon; 1985,273-310.

Janero DR. Malondialdehyde and thiobarbituric acid reactivity as diagnostic indices of lipid peroxidation and peroxidative tissue injury. Free Radic. Biol. Med. 1990, 9: 515-540.

Georgious M, Parkins LM, Payne AH. Steroid synthesis dependent, oxygen-mediated damage of mitochondrial and microsomal cytochrome P-450 enzymes in rat Leydig cell cultures. Endocrinology, 1987, 121: 1309-9.

Acharya S, Acharya UR. In vivo lipid peroxidation responses of tissues in lead treated Swiss mice. Ind. Health. 1997, 35: 542-544.

McGowan C, Donaldson WE. Changes in organ nonprotein sulfhydryl and glutathione concentrations during acute and chronic administration of inorganic lead to chicks. Biol. Trace Elem. Res., 1986, 10: 37-46.

Gayathri M, Rao Beena V, Shetty, Sudha K. Evaluation of lead toxicity and antioxidants in battery workers. Biomed. Res., 2007, 19(1): 1-4.

Mohammad IK, Mahdi AA, Raviraja A. Oxidative Stress in Painters Exposed to Low Lead Levels. Arh. Hig. Rada. Toksikol. 2008, 59: 161-169.

Batra N, Nehru B, Bansal MP. Influence of lead and zinc on rat male reproduction at biochemical and histopathological levels. J. Applied. Toxicol, 2001, 21: 507-512.

Jones R, Mann T, Sherins RJ. Peroxidation breakdown of phospholipids in human spermatozoa: Spermicidal effects of fatty acid peroxides and protective action of seminal plasma, Fertility Sterility, 1979, 31: 531-537.

Yousef M. Vitamin E modulates reproductive toxicity of pyrethroid lambdacyhalothrin in male rabbits. Food and Chemical Toxicology, 2010, 48: 1152-1159.

Oda SS, El-Maddawy Z. Protective effect of vitamin E and selenium combination on deltamethrininduced reproductive toxicity in male rats. Experimental and Toxicologic Pathology, 2012, 64: 813-819.

Yousef M, Awad T, Mohamed E. Deltamethrin-induced oxidative damage and biochemical alterations in rat and it attenuation by Vitamin E. Toxicology, 2006, 227: 240

Cerolini S, Zaniboni L, Maldjian A, Gliozzi T. Effect of docosahexaenoic acid and tocopherol enrichment in chicken sperm on semen quality, sperm lipid com- position and susceptibility to peroxidation. Theriogenology, 2006, 66: 877

Uzunhisarcikli M, Kalender Y, Dirican K, Kalender S, Ogutcu A, Buyukkomurcu F. Acute, subacute and subchronic administration of methyl parathion-induced testicular damage in male rats and protective role of vitamins C and E. Pesticide Biochemistry and Physiology 2007, 87: 115-122.

Chen H, Liu J, Luo L, Baig MU, Kim JM, Zirkin BR. Vitamin E, aging and Leydig cell steroidogenesis. Experimental Gerontology 2005, 40: 728-736.

Yue D, Yan L, Luo H, Xu X, Jin X.Effect of Vitamin E supplementation on semen quality and the testicular cell membranal and mitochondrial antioxidant abilities in Aohan fine-wool sheep. Animal Reproduction Science 2010, 118: 217-222.

Downloads

Published

2015-11-30

Issue

Section

Original Research Articles

How to Cite

1.
Enzymatic toxicity induced by lead acetate and its possible reversal by. Int Jour of Biomed Res [Internet]. 2015 Nov. 30 [cited 2026 Mar. 29];6(11):874-9. Available from: https://ssjournals.co.in/index.php/ijbr/article/view/2267