• [email protected]
  • +971 507 888 742
Submit Manuscript
SciAlert
  • Home
  • Journals
  • Information
    • For Authors
    • For Referees
    • For Librarian
    • For Societies
  • Contact
  1. Journal of Biological Sciences
  2. Vol 10 (5), 2010
  3. 396-404
  • Online First
  • Current Issue
  • Previous Issues
  • More Information
    Aims and Scope Editorial Board Guide to Authors Article Processing Charges
    Submit a Manuscript

Journal of Biological Sciences

Year: 2010 | Volume: 10 | Issue: 5 | Page No.: 396-404
DOI: 10.3923/jbs.2010.396.404
crossmark

Facebook Twitter Digg Reddit Linkedin StumbleUpon E-mail
Review Article

Male Reproductive Toxicity of Some Selected Metals: A Review

N. Mathur, G. Pandey and G.C. Jain

ABSTRACT


The management of infertility problems has become an increasingly important part of health services during the past 20 years. A substantial number of couples seek fertility treatment due to poor semen quality and there is evidence in the literature that male reproductive function seems to have deteriorated considerably in the past four-five decades. Exposure to metals is a common phenomenon due to their environmental pervasiveness. Some metals are essential for life, others have unknown biological functions, either favorable or toxic and some others have the potential to caused toxicity. Over exposure of metals are in fact, one of the oldest environmental problems and they are widely distributed in the environmental workplace. One of the major mechanisms behind metal toxicity has been attributed to oxidative stress. A growing amount of data provide evidence that metals are capable of interacting with nuclear proteins and DNA causing oxidative deterioration of biological macromolecules. The primary objective of this review is to highlight the effects of metals on male reproductive processes.
PDF Abstract XML References Citation
Received: March 16, 2010;   Accepted: May 26, 2010;   Published: July 14, 2010

How to cite this article

N. Mathur, G. Pandey and G.C. Jain, 2010. Male Reproductive Toxicity of Some Selected Metals: A Review. Journal of Biological Sciences, 10: 396-404.

DOI: 10.3923/jbs.2010.396.404

URL: https://scialert.net/abstract/?doi=jbs.2010.396.404

INTRODUCTION


It is undeniable that good quality semen is essential for reproductive success. This quality appears to have been directly affected in recent years. Since 1990s, various authors have reaffirmed that possible significant drop in sperm quality and consequently an increase in male infertility rates (Carlsen et al., 1992; Jensen et al., 2008; Traina et al., 1994). During the past 50 years, tens of thousands of metals, chemicals have been released into the general environment (Carbone et al., 2007). Over exposure of these metals cause severe damage in male reproductive health.

The use of metals has been critical to the progress and success of human civilization. It would be difficult to imagine an advanced society without extensive utilization of metallic compounds. Metals are unique among pollutant toxicants in that they are all naturally occurring and in many cases, are ubiquitous within the human environment. In addition, all life has evolved in the presence of metals and organisms have been forced to deal with these potentially toxic, yet omnipresent, elements. In fact, many metals have become essential to various biological processes. Essentiality goes hand-in-hand with intentional accumulation and safe transport, storage and usage mechanisms. Nonetheless, even essential metals will become toxic with increasing exposure. It is often the case that the nonessential toxicant metals mimic essential metals and thereby gain access to and potentially disrupt, key cellular functions. This can also account for bioaccumulation of toxic metals (Veado et al., 2006; Kutlubay et al., 2007).

Metal toxicity is believed to be mediated through macromolecules such as proteins with structural, catalytic or transport function and DNA. Reactive oxygen species are generated by metals, particularly transition metal ions e.g., of iron, copper, vanadium, cobalt, can overcome the spin restriction of O2 and donate a single electron, giving rise to free radical species and chain reaction. Toxicity occurs when such metals are free and reactions become uncontrolled. Metals also inhibit protection mechanism against reactive oxygen species, e.g., SOD, glutathione. Other important cytotoxic mechanism for some metals (e.g., mercury and chromate) are DNA damage and inhibition of cellular respiration (e.g., arsenic and chromate). Although, metals can bind to a wide variety of cellular ligands and the effects produced seem to be relatively specific for each metal (Maret and Standstead, 2006; Luebke et al., 2006).

The rapid industrialization and overgrowing urbanization, the effects of metals on male reproductive system have become major health concern globally (Chowdhury, 2009; Turgut et al., 2003). This study we reviewed metals that have been reported to produce significant toxicity in male reproductive system.

Effect of various metals on male reproduction is presented in Table 1.

Table 1: Effect of various metals on male reproduction
Image for - Male Reproductive Toxicity of Some Selected Metals: A Review
Image for - Male Reproductive Toxicity of Some Selected Metals: A Review
Image for - Male Reproductive Toxicity of Some Selected Metals: A Review
Image for - Male Reproductive Toxicity of Some Selected Metals: A Review
Image for - Male Reproductive Toxicity of Some Selected Metals: A Review

CONCLUSIONS


Increased distribution of metals and metal compounds in the environment, especially through anthropogenic activities, raises increasing concern for ecotoxicological effects. The precise chemical basis of metal toxicology is inadequately understood but a uniform mechanism for all toxic metals is implausible because of the great variation in chemical properties and toxic endpoints. Chemically, metals in their ionic form can be very reactive and can interact with biological systems in a large variety of ways. In this regard, a cell presents numerous potential metal-binding ligands. Such adventitious binding is an important chemical mechanism by which exogenous metals exert toxic effects that can result in steric re-arrangement that impairs the function of biomolecules (Kasprzak, 2002; Kasprzak et al., 2003).

Metals may operate through hormonal or genotoxic pathways to affect male reproduction. Metals may penetrate the blood testis barrier to potentially affect spermatogenesis, either by affecting genetic integrity or hormone production. Effects may be at different stages of the cell cycle such as during meiotic disjunction and such abnormalities can have deleterious effects on reproduction and offspring. Exposure to metals has been long associated with low sperm motility and density, increased morphological anomalies and male infertility.

The conclusion of present review revealed that the toxic effects of different metals depend on dose, duration, route of administration in male human and various animal species.

ACKNOWLEDGMENTS


We are greatly indebted to Professor Reena Mathur for providing facilities. The authors are also thankful to the Center for Advanced Studies, Department of Zoology, University of Rajasthan, Jaipur. Ms. Nidhi Mathur is thankful to University Grants Commission, India for providing Research Fellowship.

REFERENCES


  1. Acharya, U.R., M. Mishra, R.R. Tripathy and I. Mishra, 2006. Testicular dysfunction and antioxidative defense system of Swiss mice after chromic acid exposure. Reprod. Toxicol., 22: 87-91.
    CrossRefPubMed

  2. Acharya, U.R., R.M. Rathmore and M. Mishra, 2003. Role of vitamin C on lead acetate induced spermatogenesis in Swiss mice. Environ. Toxicol. Pharmacol., 13: 9-14.
    CrossRefDirect Link

  3. Afonne, O.J., O.E. Orisakwa, O.A. Ekanem and D.D. Akumka, 2002. Zinc protects chromium-induced testicular injury in mice. Indian J. Pharmacol., 34: 26-31.
    Direct Link

  4. Ait, H.N., M. Slimani, B. Merad-Boudia and C. Zaoui, 2009. Reproductive toxicity of lead acetate in adult male rats. Am. J. Sci. Res., 3: 38-50.

  5. Aragon, M.A., M.E. Ayala, T.I. Fortoul, P. Bizarro and M. Altamirano-Lozanod, 2005. Vanadium induced ultrastructural changes and apoptosis in male germ cells. Reprod. Toxicol., 20: 127-134.
    CrossRefDirect Link

  6. Aruldhas, M.M., S. Subramanian, P. Sekar, G. Vengatesh, G. Chandrahasan, P. Govindarajulu and M.A. Akbarsha, 2005. Chronic chromium exposure-induced changes in testicular histoarchitecture are associated with oxidative stress: Study in a non-human primate (Macaca radiata Geoffroy). Hum. Reprod., 20: 2801-2813.
    PubMed

  7. Benbrahim-Tallaa, L. and M.P. Waalkes, 2008. Inorganic arsenic and human prostate cancer. Environ Health Perspect., 116: 158-164.
    PubMed

  8. Boujbiha, M.A., K. Hamden, F. Guermazi, A. Bouslama, A. Omezzine, A. Kammoun and A. El-Feki, 2009. Testicular toxicity in mercuric chloride treated rats: Association with oxidative stress. Reprod. Toxicol., 28: 81-89.
    CrossRefPubMed

  9. Carbone, P., F. Giordano, F. Nori, A. Mantovani and D. Taruscio, 2007. The possible role of endocrine disrupting chemicals in the aetiology of cryptorchidism and hypospadias: A population-based case control study in ruralsicily. Int. J. Androl., 30: 3-13.
    CrossRefPubMed

  10. Carlsen, E., A. Giwercman, N. Keiding and N.E. Skakkebaek, 1992. Evidence for decreasing quality of semen during past 50 years. Br. Med. J., 305: 609-613.
    PubMedDirect Link

  11. Choy, C.M.Y., C.W.K. Lam, L.T.F. Cheung, C.M. Briton-Jones, L.P. Cheung and C.J. Haines, 2003. Infertility, blood mercury concentrations and dietary seafood consumption: A case-control study. Obstet. Gynecol. Surv., 58: 325-326.
    CrossRefPubMed

  12. Damjanov, I., F.W. Sunderman, J.M. Mitchell and P.R. Allpass, 1978. Induction of testicular sarcoma in Fischer rats by intratesticular injection of nickel subsulfide. Cancer Res., 38: 268-276.
    PubMed

  13. Danadevi, K., R. Rozati, P.P. Reddy and P. Grover, 2003. Semen quality of Indian welders occupationally exposed to nickel and chromium. Reprod. Toxicol., 7: 451-456.
    CrossRefPubMedDirect Link

  14. Das, K.K. and S. Dasgupta, 1997. Alteration of testicular biochemistry during protein restriction in nickel treated rats. Biol. Trace Element Res., 60: 243-249.
    CrossRefPubMed

  15. Das, K.K. and S. Dasgupta, 2002. Effect of nickel sulfate on testicular steroidogenesis in rats during protein restriction. Environ. Health Perspect., 110: 923-926.
    PubMed

  16. Dilek, B. and B. Cengiz, 2008. Protective effects of zinc on testes of cadmium-treated rats. Bull. Environ. Contam. Toxicol., 81: 521-524.
    CrossRefPubMed

  17. Doreswamy, K., B. Shrilatha, T. Rajeshkumar and Muralidhara, 2004. Nickel-induced oxidative stress in testis of mice: Evidence of DNA damage and genotoxic effects. J. Androl., 25: 996-1003.
    PubMed

  18. Elbetieha, A., A.S. Al-Tthani, R.K. Al-Thani, H. Darmani and W. Owais, 2008. Effect of chronic exposure to cobalt chloride on the fertility and testes in mice. J. Applied Biol. Sci., 2: 1-6.
    Direct Link

  19. Santos, F.W., T. Oro, G. Zeni, J.B. Rocha, P.C. do Nascimento and C.W. Nogueira, 2004. Cadmium induced testicular damage and its response to administration of succimer and diphenyl diselenide in mice. Toxicol. Lett., 152: 255-263.
    Direct Link

  20. Golub, M.S., 1992. Reproductive toxicology of water contaminants detected by routine water quality testing. Epidemiology, 3: 125-129.
    PubMed

  21. Guo, C.H., H. Chang-Jen, C. Ya-Ling and H. Guoo-Shyng, 2002. Low-dose mercury induces testicular damage protected by zinc in mice. Biol. Trace Element Res., 86: 145-157.
    CrossRefDirect Link

  22. Oliveira, H., M. Spano, C. Santos and M. de Lourdes Pereira, 2009. Lead chloride affects sperm motility and acrosome reaction in mice: Lead affects mice sperm motility and acrosome reaction. Cell Biol. Toxicol., 25: 341-353.
    CrossRef

  23. Ono, H., T. Funakoshi, H. Shimada and S. Kojima, 1997. Comparative effect of disulfiram and diethyldithiocarbamate against testicular toxicity in rats caused by acute exposure to cadmium. J. Toxicol. Environ. Health, 50: 389-400.
    PubMedDirect Link

  24. Yang, H.S., D.K. Han, J.R. Kim and J.C. Sim, 2006. Effects of α-Tocopherol on cadmium-induced toxicity in rat testis and spermatogenesis. J. Korean Med. Sci., 21: 445-451.
    CrossRefPubMedDirect Link

  25. Hsu, P.C., M.Y. Liu, C.C. Hsu, L.Y. Chen and G.Y. Leon, 1997. Lead exposure causes generation of reactive oxygen species and functional impairment in rat sperm. Toxicology, 122: 133-143.
    CrossRefPubMedDirect Link

  26. Jain, G.C., H. Pareek, S. Sharma, M. Bhardwaj and B.S. Khajja, 2007. Reproductive toxicity of vanadyle sulphate in male rats. J. Health Sci., 53: 137-141.
    Direct Link

  27. Jensen, T.K., T. Sobotka, M.A. Hansen, A.T. Pedersen, W. Lutz and N.E. Skakkebaek, 2008. Declining trends in conception rates in recent birth cohorts of native Danish women: A possible role of deteriorating male reproductive health. Int. J. Androl., 31: 81-92.
    PubMedDirect Link

  28. Cheng, J., J.L. Fu and Z.C. Zhou, 2003. The inhibitory effects of manganese on steroidogenesis in rat primary Leydig cells by disrupting steroidogenic acute regulatory (StAR) protein expression. Toxicology, 187: 139-148.
    CrossRefPubMed

  29. Kasprzak, K.S., F.W. Sunderman and K. Salnikow, 2003. Nickel carcinogenesis. Mutat. Res., 533: 67-97.
    CrossRef

  30. Kasprzak, K.S., 2002. Oxidative DNA and protein damage in metal-induced toxicity and carcinogenesis. Free Radic. Biol. Med., 32: 958-967.
    CrossRefPubMed

  31. Kaur, R. and K. Kaur, 2000. Effects of dietary selenium (SE) on morphology of testis and cauda epididymis in rats. Indian J. Physiol. Pharmacol., 44: 265-272.
    PubMedDirect Link

  32. Kaur, R. and V.R. Parshad, 1994. Effects of dietary selenium on differentiation, morphology and functions of spermatozoa of the house rat, Rattus rattus L. Mutat. Res., 309: 29-35.
    CrossRefPubMed

  33. Khan, A.T., A. Atkinson, T.C. Graham, S.J. Thompson, S. Ali and K.F. Shireen, 2004. Effects of inorganic mercury on reproductive performance of mice. Food Chem Toxicol., 42: 571-577.
    CrossRefPubMed

  34. Kim, S.K. and J.H. Kim, 2008. Inhibitory Effect of tributyltin on expression of steroidogenic enzymes in mouse testis. Int. J. Toxicol., 27: 175-182.
    CrossRefPubMed

  35. Kumasaka, K., M. Miyazawa, T. Fujimaki, H. Tao and B.R. Ramaswamy et al., 2002. Toxicity of the tributyltin compound on the testis in premature mice. J. Reprod. Dev., 48: 591-597.
    Direct Link

  36. Kutlubay, R., E.O. Oguz, B. Can, M.C. Guven, Z. Sinik and O.L. Tuncay, 2007. Vitamin E protection from testicular damage caused by intraperitoneal aluminium. Int. J. Toxicol., 26: 297-306.
    CrossRefPubMed

  37. Laskey, J.W., G.L. Rehnberg, F.J. Hein and S.C. Laws, 1985. Assessment of the male reproductive system in the preweanling rat following Mn3O4 exposure. J. Toxicol. Environ. Health, 15: 339-350.
    PubMedDirect Link

  38. Li, H., Q. Chen, S. Li, Y. Xu, W. Yao and C. Chen, 1999. Studies on male reproductive toxicity caused by hexavalent chromium. Zhonghua Yu Fang Yi Xue Za Zhi., 33: 351-353.
    PubMedDirect Link

  39. Luebke, R.W., D.H. Chen, R. Dietert, Y. Yang, M. King and M.I. Luster, 2006. The comparative immunotoxicity of five selected compounds following developmental or adult exposure. J. Toxicol. Environ. Health Part B, 9: 1-26.
    CrossRef

  40. Lukac, N., P. Massanyi, M. Zakrzewski, R. Toman, V. Cigankova and R. Stawarz, 2007. Cobalt-induced alterations in hamster testes in vivo. J. Environ. Sci. Health A Tox. Hazard. Subst. Environ. Eng., 42: 389-392.
    PubMedDirect Link

  41. Maret, W. and H. Sandstead, 2006. Zinc requirements and the risks and benefits of zinc supplementation. J. Trace Elem. Med. Biol., 20: 3-18.
    CrossRefPubMedDirect Link

  42. Martynowicz, H., R. Andrzejak and M. Medras, 2005. The influence of lead on testis function. Med. Pr., 56: 495-500.
    Direct Link

  43. Massanyi, P., N. Lukaa, J. Zemanova, A.V. Makarevich and P. Chrenek et al., 2007. Effect of nickel administration in vivo on the testicular structure in male mice. Acta Vet. Brno., 76: 223-229.
    CrossRef

  44. Massanyi, P., N. Lukac, A.V. Makarevich, P. Chrenek and Z. Forgacs et al., 2007. Lead-induced alterations in rat kidneys and testes in vivo. J. Toxicol. Environ. Health., 42: 671-676.
    CrossRef

  45. Massanyi, P., N. Lukac, J. Slivkova, J. Kovacik and A.V. Makarevich et al., 2007. Mercury-induced alterations in rat kidneys and testes in vivo. J. Environ. Sci. Health, 42: 865-870.
    CrossRefDirect Link

  46. Mayyas, I., A. Elbetieha, W. Khamas and W.A. Khamas, 2005. Evaluation of reproductive and fertility toxic potentials of aluminum chloride on adult male mice. J. Anim. Vet. Adv., 4: 224-233.

  47. Meeker, J.D., M.G. Rossano, B. Protas, M.P. Diamond and E. Puscheck et al., 2008. Cadmium, lead and other metals in relation to semen quality: Human evidence for molybdenum as a male reproductive toxicant. Environ. Health Perspect., 116: 1473-1479.
    CrossRefPubMedDirect Link

  48. Misawa, Y., K. Watanabe, T. Sakurai, E. Fujii, K. Tsukamoto, A. Kato and T. Sugimoto, 2000. Collaborative work to evaluate toxicity on male reproductive organs by repeated dose studies in rats. Testicular toxicity of 2- or 4-week repeated or single-dose administration of a novel platinum complex. J. Toxicol. Sci., 25: 117-127.
    PubMedDirect Link

  49. Monsefi, M., S. Alaee, A. Moradshahi and L. Rohani, 2010. Cadmium-induced infertility in male mice. Environ. Toxicol., 25: 94-102.
    CrossRefPubMedDirect Link

  50. Mukherjee, S. and P.K. Mukhopadhyay, 2009. Studies on arsenic toxicity in male rat gonads and its protection by high dietary protein supplementation. Al Ameen J. Med. Sci., 2: 73-77.
    Direct Link

  51. Omura, M., R. Ogata, K. Kubo, Y. Shimasaki and S. Aou et al., 2001. Two-generation reproductive toxicity study of tributyltin chloride in male rats. Toxicol. Sci., 64: 224-232.
    PubMedDirect Link

  52. Omura, M., A. Tanaka, M. Hirata, M. Zhao and Y. Makita et al., 1996. Testicular toxicity of gallium arsenide, indium arsenide and arsenic oxide in rats by repetitive intratracheal instillation. Fundam. Appl. Toxicol., 32: 72-78.
    CrossRefPubMedDirect Link

  53. Orisakwe, O.E., O.J. Afonne, E. Nwobodo, L. Asomugha and C.E. Dioka, 2001. Low-dose mercury induces testicular damage protected by zinc in mice. Eur. J. Obstet. Gynecol. Reprod. Biol., 95: 92-96.
    CrossRefPubMed

  54. Pandey, R., R. Kumar, S.P. Singh, D.K. Saxena and S.P. Srivastava, 1999. Male reproductive effect of nickel sulphate in mice. BioMetals, 12: 339-346.
    PubMedDirect Link

  55. Pandey, R. and S.P. Singh, 2002. Effects of molybdenum on fertility of male rats. Biometals, 15: 65-72.
    CrossRefDirect Link

  56. Pandey, R. and S.P. Srivastava, 2000. Spermatotoxic effects of nickel in mice. Bull. Environ. Contam. Toxicol., 64: 161-167.
    CrossRefPubMedDirect Link

  57. Pant, N., R. Kumar, R.C. Murthy and S.P. Srivastava, 2001. Male reproductive effect of arsenic in mice. BioMetals, 14: 113-117.
    CrossRefPubMedDirect Link

  58. Pant, N., R.C. Murthy and S.P. Srivastava, 2004. Male reproductive toxicity of sodium arsenite in mice. Human Exp. Toxicol., 23: 399-403.
    CrossRef

  59. Ponnapakkam, T.P., K.S. Bailey, K.A. Graves and M.B. Iszard, 2003. Assessment of male reproductive system in the CD-1 mice following oral manganese exposure. Reprod. Toxicol., 7: 547-551.
    CrossRefPubMedDirect Link

  60. Manna, P., M. Sinha and P.C. Sil, 2008. Protection of arsenic-induced testicular oxidative stress by arjunolic acid. Redox Rep., 13: 67-77.
    PubMed

  61. Ragan, H.A. and T.J. Mast, 1990. Cadmium inhalation and male reproductive toxicity. Rev. Environ. Contam. Toxicol., 114: 1-22.
    PubMedDirect Link

  62. Rao, M.V. and P.S. Sharma, 2001. Protective effect of vitamin E against mercuric chloride reproductive toxicity in male mice. Reprod. Toxicol., 15: 705-712.
    CrossRefPubMedDirect Link

  63. Kakela, R., A. Kakela and H. Hyvarinen, 1999. Effects of nickel chloride on reproduction of the rat and possible antagonistic role of selenium. Comp. Biochem. Physiol. C Pharmacol. Toxicol. Endocrinol., 123: 27-37.
    PubMedDirect Link

  64. Rignell-Hydbom, A., A. Axmon, T. Lundh, B.A. Jonsson, T. Tiido and M. Spano, 2007. Dietary exposure to methyl mercury and PCB and the associations with semen parameters among Swedish fishermen. Environ. Health, 6: 14-14.
    CrossRefPubMedDirect Link

  65. Romera, E.P., E. Munoz, F. Mohamed, S. Dominguez and L. Scardapane et al., 2000. Lithium effect on testicular tissue and spermatozoa of viscacha (Lagostomus maximus). A comparative study with rats. J. Trace Elem. Med. Biol., 14: 81-83.
    PubMedDirect Link

  66. Sarkar, M., G.R. Chaudhuri, A. Chattopadhyay and N.M. Biswas, 2003. Effect of sodium arsenite on spermatogenesis, plasma gonadotrophins and testosterone in rats. Asian J. Androl., 5: 27-31.
    Direct Link

  67. Seethalakshmi, L., C. Flores, T. Kinkead, A.A. Carboni, R.K. Malhotra and M. Menon, 1992. Effects of subchronic treatment with cis-platinum on testicular function, fertility, pregnancy outcome and progeny. J. Androl., 13: 65-74.
    PubMedDirect Link

  68. Siu, E.R., D.D. Mruk, C.S. Porto and C.Y. Cheng, 2009. Cadmium-induced testicular injury. Toxicol. Applied Pharmacol., 238: 240-249.
    CrossRefDirect Link

  69. Slivkova, J., M. Popelkova, P. Massanyi, S. Toporcerova and R. Stawarz et al., 2009. Concentration of trace elements in human semen and relation to spermatozoa quality. J. Environ. Sci. Health Part A Toxic/Hazard. Subst. Environ. Eng., 44: 370-375.
    CrossRefPubMedDirect Link

  70. Sokol, R.Z. and N. Berman, 1991. The effect of age of exposure on lead-induced testicular toxicity. Toxicology, 69: 269-278.
    CrossRefPubMed

  71. Subramanian, S., G. Rajendiran, P. Sekhar, C. Gowri, P, Govindarajulu and M.M. Aruldhas, 2006. Reproductive toxicity of chromium in adult bonnet monkeys (Macaca radiata Geoffrey). Reversible oxidative stress in the semen. Toxicol. Applied Pharmacol., 215: 237-249.
    CrossRefPubMed

  72. Telisman, S., B. Colak, A. Pizent, J. Jurasovic and P. Cvitkovic, 2007. Reproductive toxicity of low-level lead exposure in men. Environ. Res., 105: 256-266.
    CrossRefPubMedDirect Link

  73. Thakur, S.C., S.S. Thakur, S.K. Chaube and S.P. Singh, 2003. Subchronic supplementation of lithium carbonate induces reproductive system toxicity in male rat. Reprod. Toxicol., 17: 683-690.
    Direct Link

  74. Thomas, J.W. and S. Moos, 1951. The effect of orally administered molybdenum on growth, spermatogenesis and testes histology of young dairy bulls. Arch. Biochem., 15: 81-88.
    Direct Link

  75. Traina, M.E., P. Ade, G. Siepi, E. Urbani and M.G. Petrelli, 1994. A review of the effect of pesticide formulations on male fertility. Int. J. Environ. Health Res., 4: 38-47.
    CrossRefDirect Link

  76. Turgut, G., G. Abban, S. Turgut and G. Take, 2003. Effect of Overdose Zinc on mouse testis and its relation with sperm count and motility. Biol. Trace Elem. Res., 96: 271-278.
    CrossRefDirect Link

  77. Veado, M.A.R.V., I.A. Arante, A.H. Oliveira, M.R.M.G. Almeida, R.A. Miguel, M.I. Severo and H.L. Cabaleiro, 2006. Metal pollution in the environment of minas gerais state-Brazil. Environ. Monit. Assess., 117: 157-172.
    CrossRefDirect Link

  78. Waltschewa, W., M. Slatewa and I. Michailow, 1972. Testicular changes due to long-term administration of nickel sulphate in rats. Exp. Pathol. (Jena)., 6: 116-120.
    PubMedDirect Link

  79. Yasmina, M. and C. Abdennour, 2008. Influence of vitamin C on testicular functions of domestic rabbit Oryctolagus cuniculus under mercury exposure. Eur. J. Sci. Res., 22: 197-204.
    Direct Link

  80. Yousef, M.I., F.M. El-Demerdash, K.I. Kamil and F.A.M. Elaswad, 2006. Ameliorating effect of folic acid on chromium (VI)-induced changes in reproductive performance and seminal plasma biochemistry in male rabbits. Reprod. Toxicol., 21: 322-328.
    PubMed

  81. Yousef, M.I., A.M. El-Morsy and M.S. Hassan, 2005. Aluminium-induced deterioration in reproductive performance and seminal plasma biochemistry of male rabbits: Protective role of ascorbic acid. Toxicology, 215: 97-107.
    CrossRefPubMedDirect Link

  82. Zarnescu, O. and G. Zamfirescu, 2006. Effects of lithium carbonate on rat seminiferous tubules: An ultrastructural study. Int. J. Androl., 29: 576-582.
    PubMedDirect Link

  83. Amara, S., H. Abdelmelek, C. Garrel, P. Guiraud and T. Douki et al., 2008. Preventive effect of zinc against cadmium-induced oxidative stress in the rat testis. J. Reprod. Dev., 54: 129-134.
    PubMed

  84. Waalkes, M.P., S. Rehm and D.E. Devor, 1997. The effects of continuous testosterone exposure on spontaneous and cadmium-induced tumors in the male Fischer (F344/NCr) rat: Loss of testicular response. Toxicol. Applied Pharmacol., 142: 40-46.
    PubMed

  85. Chowdhury, A.R., 2009. Recent advances in heavy metals induced effect on male reproductive function-A retrospective. Al Ameen J. Med. Sci., 2: 37-42.

  86. Mathur, A.K., S.V. Chandra, J. Behari and S.K. Tandon, 1977. Biochemical and morphological changes in some organs of rats in nickel intoxication. Arch. Toxicol., 37: 159-164.
    CrossRefDirect Link

Related Articles

Evaluation of Reproductive and Fertility Toxic Potentials of Aluminum Chloride on Adult Male Mice

Comments


vinayakam prakash Reply
25 November, 2011

i am also in same research i think lead is more toxic sub stance to decrease the sperm motility in uterus and
also cause infertility.

Leave a Comment


Your email address will not be published. Required fields are marked *

Useful Links

  • Journals
  • For Authors
  • For Referees
  • For Librarian
  • For Socities

Contact Us

Office Number 1128,
Tamani Arts Building,
Business Bay,
Deira, Dubai, UAE

Phone: +971 507 888 742
Email: [email protected]

About Science Alert

Science Alert is a technology platform and service provider for scholarly publishers, helping them to publish and distribute their content online. We provide a range of services, including hosting, design, and digital marketing, as well as analytics and other tools to help publishers understand their audience and optimize their content. Science Alert works with a wide variety of publishers, including academic societies, universities, and commercial publishers.

Follow Us
© Copyright Science Alert. All Rights Reserved