Volume 11, Issue 7 (10-2013)                   IJRM 2013, 11(7): 577-0 | Back to browse issues page

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Babaei H, Abshenas J. Zinc therapy improves adverse effects of long term administration of copper on epididymal sperm quality of rats. IJRM 2013; 11 (7) :577-0
URL: http://ijrm.ir/article-1-439-en.html
1- Department of Clinical Sciences, Faculty of Veterinary Medicine, Shahid Bahonar University of Kerman, Kerman, Iran , Babaei_H@mail.uk.ac.ir
2- Department of Clinical Sciences, Faculty of Veterinary Medicine, Shahid Bahonar University of Kerman, Kerman, Iran
Abstract:   (2363 Views)
Background: Industrial copper ingest is a common form of poisoning in animals. Zinc has an important role in the physiology of spermatozoa, in sperm production and viability.
Objective: This study was set to investigate whether the adverse effects of long term copper consumption on quality of rat spermatozoa could be prevented by zinc therapy.
Materials and Methods: Forty eight mature (6-8 weeks old) male rats were randomly allocated to either control (Cont, n=12) or three treatment groups each containing twelve animals. Animals in the first treatment group was gavaged with copper sulfate, the second treatment group was injected with zinc sulfate, and the third treatment group was given combined treatment of copper and zinc. Control animals received normal saline using the same volume and similar methods. Six rats from each group were sacrificed on day 28 and 56 after treatments for sperm quality evaluations.
Results: In spite of testicular weight reduction 56 days after copper consumption in comparison to the control group (p=0.002), there was not a significant difference between the control and combined treatment of copper and zinc group (31.40±0.55 vs. 28.63±0.55, p=0.151). Administration of copper caused a significant decrease in the sperm count, viability and motility after 56 days compared to the control group. However, a complete recovery in sperm count was seen in combined treatment of copper and zinc group after 56 days compared to the control group (p=0.999) and a partial improvement was seen about the percentage of viability and motility (p<0.001).
Conclusion: Adverse effects of long term consumption of copper on sperm quality could be prevented by zinc therapy in rats.
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Type of Study: Original Article |

References
1. Elgerwi A, Bires J, Levkut M. Industrial copper intoxication in sheep: clinical and pathological findings. Acta Vet Brno 1999; 68: 197-202. [DOI:10.2754/avb199968030197]
2. Boubsil S, Abdennour C, Tegurin M. Assessment of some blood biomarkers of workmen from a copper wire factory. Annals Biol Res 2011; 2: 164-169.
3. Bidewell C, Livesey C. Copper poisoning: anemerging disease in dairy cattle. State Vet J 2002; 12: 16-19.
4. Sakhaee E, Emadi L, Abshenas J, Kheirandish R, Azari O, Amiri E. Evaluation of epididymal sperm quality following experimentally induced copper poisoning in male rats. Andrologia 2012; 44 (Suppl.): 110-116. [DOI:10.1111/j.1439-0272.2010.01147.x]
5. Kupper J, Bidaut A, Waldvogel A, Emmenegger B, Naegeli H. [Treatment of chronic copper poisoning in dairy sheep with oral ammonium molybdate and sodium sulphate ]. Schweiz Arch Tierheilkd 2005; 147: 219-224. (in German) [DOI:10.1024/0036-7281.147.5.219]
6. Christodoulopoulos G, Roubies N. Diagnosis and treatment of copper poisoning caused by accidental feeding on poultry litter in a sheep flock. Aust Vet J 2007; 85: 451-453. [DOI:10.1111/j.1751-0813.2007.00186.x]
7. Lewis-Jones DI, Aird IA, Biljan MM, Kingsland CR. Effects of sperm activity on zinc and fructose concentrations in seminal plasma. Hum Reprod 1996; 11: 2465-2467. [DOI:10.1093/oxfordjournals.humrep.a019138]
8. Bjorndahl L, Kvist U. A model for the importance of zinc in the dynamics of human sperm chromatin stabilization after ejaculation in relation to sperm DNA vulnerability. Syst Biol Reprod Med 2011; 57: 86-92. [DOI:10.3109/19396368.2010.516306]
9. Bremner I, Marshall RB. Hepatic copper- and zinc-binding proteins in ruminants. Relationship between Cu and Zn concentrations and the occurrence of a metallothionein-like fraction. Br J Nutr 1974; 32: 293-300. [DOI:10.1079/BJN19740082]
10. Bremner I, Young BW, Mills CF. Protective effect of zinc supplementation against copper toxicosis in sheep. Br J Nutr 1976; 36: 551-561. [DOI:10.1079/BJN19760108]
11. Ghasemi N, Babaei H, Azizallahi S, Kheradmand A. Effect of long-term administration of zinc after scrotal heating on mice spermatozoa and subsequent offspring quality. Andrologia 2009; 41: 222-228. [DOI:10.1111/j.1439-0272.2009.00920.x]
12. Sullivan JM, Janovitz EB, Robinson FR. Copper toxicosis in veal calves. J Vet Diagn Invest 1991; 3: 161-164. [DOI:10.1177/104063879100300211]
13. Hamar DW, Bedwell CL, Johnson JL, Schultheiss PC, Raisbeck M, Grotelueschen DM, et al. Iatrogenic copper toxicosis induced by administering copper oxide boluses to neonatal calves. J Vet Diagn Invest 1997; 9: 441-443. [DOI:10.1177/104063879700900422]
14. Steffen DJ, Carlson MP, Casper HH. Copper toxicosis in suckling beef calves associated with improper administration of copper oxide boluses. J Vet Diagn Invest 1997; 9: 443-446. [DOI:10.1177/104063879700900423]
15. Minervino AH, Barreto Junior RA, Ferreira RN, Rodrigues FA, Headley SA, Mori CS, et al. Clinical observations of cattle and buffalos with experimentally induced chronic copper poisoning. Res Vet Sci 2009; 87: 473-478. [DOI:10.1016/j.rvsc.2009.05.002]
16. Araya M, Kelleher SL, Arredondo MA, Sierralta W, Vial MT, Uauy R, et al. Effects of chronic copper exposure during early life in rhesus monkeys. Am J Clin Nutr 2005; 81: 1065-1071. [DOI:10.1093/ajcn/81.5.1065]
17. Lohmiller JJ, Swing SP. Reproduction and Breeding. In: Suckow MA, Weisbroth SH, Franklin CL (eds) The Laboratory Rat. 2nd Ed. Elsevier Academic Press, London, UK, 2006; 153. [DOI:10.1016/B978-012074903-4/50009-1]
18. Wu W, Zhang Y, Zhang F. [Studies on semen quality in workers exposed to manganese and electric welding]. Chung Hua Yu Fang I Hsuch Tsa Chih 1996; 30: 266-271. (in Chinese)
19. Zhang SS, Noordin MM, Rahman SO, Haron J. Effects of copper overload on hepatic lipid peroxidation and antioxidant defense in rats. Vet Hum Toxicol 2000; 42: 261-264.
20. Linder MC, Hazegh-Azam M. Copper biochemistry and molecular biology. Am J Clin Nutr 1996; 63: 797S-811S.
21. Pourahmad J, O'Brien PJ. A comparison of hepatocyte cytotoxic mechanisms for Cu2+ and Cd2+. Toxicology 2000; 143: 263-273. [DOI:10.1016/S0300-483X(99)00178-X]
22. Gaetke LM, Chow CK. Copper toxicity, oxidative stress, and antioxidant nutrients. Toxicology 2003; 189: 147-163. [DOI:10.1016/S0300-483X(03)00159-8]
23. Kerr JF, Wyllie AH, Currie AR. Apoptosis: a basic biological phenomenon with wide-ranging implications in tissue kinetics. Br J Cancer 1972; 26: 239-257. [DOI:10.1038/bjc.1972.33]
24. Aston NS, Watt N, Morton IE, Tanner MS, Evans GS. Copper toxicity affects proliferation and viability of human hepatoma cells (HepG2 line). Hum Exp Toxicol 2000; 19: 367-376. [DOI:10.1191/096032700678815963]
25. Kang J, Lin C, Chen J, Liu Q. Copper induces histone hypoacetylation through directly inhibiting histone acetyltransferase activity. Chem Biol Interact 2004; 148: 115-123. [DOI:10.1016/j.cbi.2004.05.003]
26. Shaheen AA, el-Fattah AA. Effect of dietary zinc on lipid peroxidation, glutathione, protein thiols levels and superoxide dismutase activity in rat tissues. Int J Biochem Cell Biol 1995; 27: 89-95. [DOI:10.1016/1357-2725(94)00053-0]
27. Sokol RJ, Devereaux M, Mierau GW, Hambidge KM, Shikes RH. Oxidant injury to hepatic mitochondrial lipids in rats with dietary copper overload. Modification by vitamin E deficiency. Gastroenterology 1990; 99: 1061-1071. [DOI:10.1016/0016-5085(90)90627-D]
28. Burke JP, Fenton MR. Effect of a zinc-deficient diet on lipid peroxidation in liver and tumor subcellular membranes. Proc Soc Exp Biol Med 1985; 179: 187-191. [DOI:10.3181/00379727-179-42083]
29. Mankad M, Sathawara NG, Doshi H, Saiyed HN, Kumar S. Seminal plasma zinc concentration and alpha-glucosidase activity with respect to semen quality. Biol Trace Elem Res 2006; 110: 97-106. [DOI:10.1385/BTER:110:2:97]
30. Kendall NR, McMullen S, Green A, Rodway RG. The effect of a zinc, cobalt and selenium soluble glass bolus on trace element status and semen quality of ram lambs. Anim Reprod Sci 2000; 62: 277-283. [DOI:10.1016/S0378-4320(00)00120-2]
31. Zhao RP, Xiong CL. [Zinc content analysis in serum, seminal plasma and spermatozoa of asthenozoospermic and oligoasthenozoospermic patients]. Zhonghua Nan Ke Xue 2005; 11: 680-682. (in Chinese)
32. Chia SE, Ong CN, Chua LH, Ho LM, Tay SK. Comparison of zinc concentrations in blood and seminal plasma and the various sperm parameters between fertile and infertile men. J Androl 2000; 21: 53-57.
33. Hafez ESE, Hafez B. Reproduction in Farm Animals. Lippincott Williams and Wilkins, Philadelphia, USA; 2000. [DOI:10.1002/9781119265306]
34. Hidiroglou M, Knipfel JE. Zinc in mammalian sperm: a review. J Dairy Sci 1984; 67: 1147-1156. [DOI:10.3168/jds.S0022-0302(84)81416-2]
35. Sharif R, Thomas P, Zalewski P, Fenech M. The role of zinc in genomic stability. Mutat Res 2012; 733: 111-121. [DOI:10.1016/j.mrfmmm.2011.08.009]
36. Favier AE. The role of zinc in reproduction. Hormonal mechanisems. Biol Trace Elem Res 1992; 32: 363-382. [DOI:10.1007/BF02784623]
37. Chimienti F, Aouffen M, Favier AE, Seve M. Zinc homeostasis regulating proteins: new drug tergets for triggering cell fate. Curr Drug Targets 2003; 4: 323-338. [DOI:10.2174/1389450033491082]
38. Zago M, Oteiza PI. The antioxidant properties of zinc: interactions with iron and antioxidants. Free Rad Biol Med 2001; 31: 266-274. [DOI:10.1016/S0891-5849(01)00583-4]

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