Volume 14, Issue 1 (1-2016)                   IJRM 2016, 14(1): 47-52 | Back to browse issues page


XML Persian Abstract Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Eskandari F, Momeni H R. Silymarin protects plasma membrane and acrosome integrity in sperm treated with sodium arsenite. IJRM 2016; 14 (1) :47-52
URL: http://ijrm.ir/article-1-686-en.html
1- Department of Biology, Faculty of Science, Arak University, Arak, Iran
2- Department of Biology, Faculty of Science, Arak University, Arak, Iran , h-momeni@araku.ac.ir
Abstract:   (2388 Views)
Background: Exposure to arsenic is associated with impairment of male reproductive function by inducing oxidative stress. Silymarin with an antioxidant property scavenges free radicals.
Objective: The aim of this study was to investigate if silymarin can prevent the adverse effects of sodium arsenite on ram sperm plasma membrane and acrosome integrity.
Materials and Methods: Ram epidydimal spermatozoa were divided into five groups: spermatozoa at 0 hr, spermatozoa at 180 min (control), spermatozoa treated with silymarin (20 μM) + sodium arsenite (10 μM) for 180 min, spermatozoa treated with sodium arsenite (10 μM) for 180 min and spermatozoa treated with silymarin (20 μM) for 180 min. Double staining of Hoechst and propidium iodide was performed to evaluate sperm plasma membrane integrity, whereas comassie brilliant blue staining was used to assess acrosome integrity.
Results: Plasma membrane (p< 0.001) and acrosome integrity (p< 0.05) of the spermatozoa were significantly reduced in sodium arsenite group compared to the control. In silymarin + sodium arsenite group, silymarin was able to significantly (p< 0.001) ameliorate the adverse effects of sodium arsenite on these sperm parameters compared to sodium arsenite group. The incubation of sperm for 180 min (control group) showed a significant (p< 0.001) decrease in acrosome integrity compared to the spermatozoa at 0 hour. The application of silymarin alone for 180 min could also significantly (p< 0.05) increase sperm acrosome integrity compared to the control.
Conclusion: Silymarin as a potent antioxidant could compensate the adverse effects of sodium arsenite on the ram sperm plasma membrane and acrosome integrity.
Full-Text [PDF 456 kb]   (823 Downloads) |   |   Full-Text (HTML)  (512 Views)  
Type of Study: Original Article |

References
1. Mukherjee S, Mukhopadhyay P. Studies on arsenic toxicity in male rat gonads and its protection by high dietary protein supplementation. Al Ameen J Med Sci 2009; 2: 73-77.
2. Hughes JP, Polissar L, Vanbelle G. Evaluation and synthesis of health effects studies of communities surrounding arsenic producing industries. Int J Epidemiol 1988; 17: 407-413. [DOI:10.1093/ije/17.2.407]
3. Chou W-C, Dang C V. Acute promyelocytic leukemia: recent advances in therapy and molecular basis of response to arsenic therapies. Curr Opin Hematol 2005; 12: 1-6. [DOI:10.1097/01.moh.0000148552.93303.45]
4. Hu J, Fang J, Dong Y, Chen SJ, Chen Z. Arsenic in cancer therapy. Anticancer Drugs 2005; 16: 119-127. [DOI:10.1097/00001813-200502000-00002]
5. Akter KF, Owens G, Davey DE, Naidu R. Arsenic speciation and toxicity in biological systems. Springer; 2005. [DOI:10.1007/0-387-27565-7_3]
6. Kannan GM, Flora SJS. Chronic arsenic poisoning in the rat: treatment with combined administration of succimers and an antioxidant. Ecotoxicol Environ Saf 2004; 58: 37-43. [DOI:10.1016/S0147-6513(03)00096-4]
7. Wang A, Holladay SD, Wolf DC, Ahmed SA, Robertson JL. Reproductive and developmental toxicity of arsenic in rodents: a review. Int J Toxicol 2006; 25: 319-331. [DOI:10.1080/10915810600840776]
8. Soleimani Mehranjani M, Hemadi M. The effects of sodium arsenite on the testis structure and sex hormones in vasectomised rats. Iran J Reprod Med 2007; 5: 127-133.
9. Sarkar M, Chaudhuri GR, Chattopadhyay A, Biswas NM. Effect of sodium arsenite on spermatogenesis, plasma gonadotrophins and testosterone in rats. Asian J Androl 2003; 5: 27-32.
10. Ahmad I, Hussain T, Akthar K. Arsenic induced microscopic changes in rat testis. Prof Med J 2008; 15: 287-291.
11. Jana K, Jana S, Samanta PK. Effects of chronic exposure to sodium arsenite on hypothalamo-pituitary-testicular activities in adult rats: possible an estrogenic mode of action. Reprod Biol Endocrinol 2006; 4: 1-13. [DOI:10.1186/1477-7827-4-9]
12. Momeni HR, Eskandari N. Effect of vitamin E on sperm parameters and DNA integrity in sodium arsenite-treated rats. Iran J Reprod Med 2012; 10: 249-256.
13. Pant N, Murthy RC, Srivastava SP. Male reproductive toxicity of sodium arsenite in mice. Hum Exp Toxicol 2004; 23: 399-403. [DOI:10.1191/0960327104ht467oa]
14. Chang SI, Jin B, Youn P, Park C, Park J-D, Ryu D-Y. Arsenic-induced toxicity and the protective role of ascorbic acid in mouse testis. Toxicol Appl Pharmacol 2007; 218: 196-203. [DOI:10.1016/j.taap.2006.11.009]
15. Hadaruga DI, Hadaruga NG. Antioxidant activity of hepatoprotective Silymarin and Silybum marianum L. extract. Chem Bull 2009; 54: 2.
16. Nencini C, Giorgi G, Micheli L. Protective effect of silymarin on oxidative stress in rat brain. Phytomedicine 2007; 14: 129-135. [DOI:10.1016/j.phymed.2006.02.005]
17. Bongiovanni GA, Soria EA, Eynard AR. Effects of the plant flavonoids silymarin and quercetin on arsenite-induced oxidative stress in CHO-K1 cells. Food Chem Toxicol 2007; 45: 971-976. [DOI:10.1016/j.fct.2006.12.002]
18. Organization WH. WHO laboratory manual for the examination of human semen and sperm-cervical mucus interaction. Cambridge university press; 1999.
19. Sutradhar BC, Park J, Hong G, Choi SH, Kim G, others. Effects of trypsinization on viability of equine chondrocytes in cell culture. Pak Vet J 2010; 30: 232-238.
20. Feng HL, Han YB, Hershlag A, Zheng LJ. Impact of Ca2+ flux inhibitors on acrosome reaction of hamster spermatozoa. J Androl 2007; 28: 561-564. [DOI:10.2164/jandrol.106.001958]
21. Hosseini M-J, Shaki F, Ghazi-Khansari M, Pourahmad J. Toxicity of arsenic (III) on isolated liver mitochondria: A new mechanistic approach. Iran J Pharm Res 2013; 12 (Suppl.): 121.
22. Lash LH. Mitochondrial glutathione transport: physiological, pathological and toxicological implications. Chem Biol Interact 2006; 163: 54-67. [DOI:10.1016/j.cbi.2006.03.001]
23. Vernet P, Aitken RJ, Drevet JR. Antioxidant strategies in the epididymis. Mol Cell Endocrinol 2004; 216: 31-39. [DOI:10.1016/j.mce.2003.10.069]
24. Kohno H, Tanaka T, Kawabata K, Hirose Y, Sugie S, Tsuda H, et al. Silymarin, a naturally occurring polyphenolic antioxidant flavonoid, inhibits azoxymethane-induced colon carcinogenesis in male F344 rats. Int J Cancer 2002; 101: 461-468. [DOI:10.1002/ijc.10625]
25. Ickowicz D, Finkelstein M, Breitbart H. Mechanism of sperm capacitation and the acrosome reaction: role of protein kinases. Asian J Androl 2012; 14: 816. [DOI:10.1038/aja.2012.81]
26. Florea A-M, Yamoah EN, Dopp E. Intracellular calcium disturbances induced by arsenic and its methylated derivatives in relation to genomic damage and apoptosis induction. Environ Health Perspect 2005; 113: 659. [DOI:10.1289/ehp.7634]
27. Peris S, Solanes D, Pe-a A, Enric-Rodríguez-Gil J, Rigau T. Ion-mediated resistance to osmotic changes of ram spermatozoa: the role of amiloride and ouabain. Theriogenology 2000; 54: 1453-1467. [DOI:10.1016/S0093-691X(00)00467-2]

Send email to the article author


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

Designed & Developed by : Yektaweb