Orally administered Chrysin improves post-thawed sperm quality and fertility of rooster

Reproduction in Domestic Animals

Volumn 52, Issue 6, 2017, Pages 1004-1010

  Zhandi, M ^a   Ansari, M ^a   Roknabadi, P ^a   Zare Shahneh, A ^a   Sharafi, M ^b,c  

^a UNIVERSITY OF TEHRAN   (Iran)

^b TARBIAT MODARES UNIVERSITY   (Iran)

^c ROYAN INSTITUTE FOR REPRODUCTIVE BIOMEDICINE   (Iran)

Author keywords

antioxidant; cryopreservation; fertility; semen

Indexed keywords

CHRYSIN; FLAVONOID;

ANIMAL; ARTIFICIAL INSEMINATION; CHICKEN; CRYOPRESERVATION; DIET; DRUG EFFECT; FEMALE; FERTILITY; MALE; PHYSIOLOGY; SEMEN ANALYSIS; SPERM PRESERVATION; SPERMATOZOON; SPERMATOZOON MOTILITY; VETERINARY MEDICINE;

ANIMALS; CHICKENS; CRYOPRESERVATION; DIET; FEMALE; FERTILITY; FLAVONOIDS; INSEMINATION, ARTIFICIAL; MALE; SEMEN ANALYSIS; SEMEN PRESERVATION; SPERM MOTILITY; SPERMATOZOA;

EID: 85023195706     PISSN: 09366768     EISSN: 14390531     Source Type: Journal    
DOI: 10.1111/rda.13014     Document Type: Article

References (40)

1. Abouelezz, F. M. K., Castano, C., Toledano-Diaz, A., Esteso, M. C., Lopez-Sebastian, A., Campo, J. L., & Santiago-Moreno, J. (2015). Sperm-egg penetration assay assessment of the contraceptive effects of glycerol and egg yolk in rooster sperm diluents. Theriogenology, 83, 1541–1547.
2. Agarwal, A., Virk, G., Ong, C., & du Plessis, S. S. (2014). Effect of oxidative stress on male reproduction. The World Journal of Men's Health, 32, 1–17.
3. Aksu, E. H., Ozkaraca, M., Kandemir, F. M., Omur, A. D., Eldutar, E., Kucukler, S., & Comakli, S. (2016). Mitigation of paracetamol-induced reproductive damage by chrysin in male rats via reducing oxidative stress. Andrologia, 48, 1145–1154.
4. Amini, M. R., Kohram, H., Zare Shahaneh, A., Zhandi, M., Sharideh, H., & Nabi, M. M. (2015b). The effects of different levels of vitamin E and vitamin C in modified Beltsville extender on rooster post-thawed sperm quality. Cell Tissue Bank, 16, 587–592.
5. Amini, M. R., Kohram, H., Zare-Shahaneh, A., Zhandi, M., Sharideh, H., & Nabi, M. M. (2015a). The effects of different levels of catalase and superoxide dismutase in modified Beltsville extender on rooster post-thawed sperm quality. Cryobiology, 70, 226–232.
6. Ansari, M., Zhandi, M., Kohram, H., Zaghari, M., Sadeghi, M., & Sharafi, M. (2017). Improvement of post-thawed sperm quality and fertility of Arian rooster by oral administration of d-aspartic acid. Theriogenology, 92, 69–74.
7. Athayde, K. S., Cocuzza, M., Agarwal, A., Krajcir, N., Lucon, A. M., Srougi, M., & Hallak, J. (2007). Development of normal reference values for seminal reactive oxygen species and their correlation with leukocytes and semen parameters in a fertile population. Journal of Andrology, 28, 613–620.
8. Benesova, B., & Trefil, P. (2016). Possibilities for preserving genetic resources in birds. World's Poultry Science Journal, 72, 628–641.
9. Cedikova, M., Miklikova, M., Stachova, L., Grundmanova, M., Tuma, Z., Vetvicka, V., … Kuncova, J. (2014). Effects of the Czech Propolis on sperm mitochondrial function. Evidence-Based Complementary and Alternative Medicine, 2014, 1–10.
10. Chatterjee, S., & Gagnon, C. (2001). Production of reactive oxygen species by spermatozoa undergoing cooling, freezing, and thawing. Molecular Reproduction and Development, 59, 451–458.
11. Ciftci, O., Ozdemir, I., Aydin, M., & Beytur, A. (2012). Beneficial effects of chrysin on the reproductive system of adult male rats. Andrologia, 44, 181–186.
12. Darwish, H. A., Arab, H. H., & Abdelsalam, R. M. (2014). Chrysin alleviates testicular dysfunction in adjuvant arthritic rats via suppression of inflammation and apoptosis: Comparison with celecoxib. Toxicology and Applied Pharmacology, 279, 129–140.
13. Dhawan, K., Kumar, S., & Sharma, A. (2002). Beneficial effects of chrysin and benzoflavone on virility in 2-year-old male rats. Journal of Medicinal Food, 5, 43–48.
14. Gharagozloo, P., & Aitken, R. J. (2011). The role of sperm oxidative stress in male infertility and the significance of oral antioxidant therapy. Human Reproduction, 26, 1628–1640.
15. Giraud, M. N., Motta, C., Boucher, D., & Grizard, G. (2000). Membrane fluidity predicts the outcome of cryopreservation of human spermatozoa. Human Reproduction, 15, 2160–2164.
16. Kumar, S., & Pandey, A. K. (2013). Chemistry and biological activities of flavonoids: An Overview. Scientific World Journal, 2013, 1–16.
17. Long, J. A. (2006). Avian semen cryopreservation: What are the biological challenges? Poultry Science, 85, 232–236.
18. Madeddu, M., Mosca, F., Abdel Sayed, A., Zaniboni, L., Mangiagalli, M. G., Colombo, E., & Cerolini, S. (2016). Effect of cooling rate on the survival of cryopreserved rooster sperm: Comparison of different distances in the vapor above the surface of the liquid nitrogen. Animal Reproduction Science, 171, 58–64.
19. Mandal, R., Badyakar, D., & Chakrabarty, J. (2014). Role of membrane lipid fatty acids in sperm cryopreservation. Advances in Andrology, 2014, 1–9.
20. Mantawy, E. M., El-Bakly, W. M., Esmat, A., Badr, A. M., & El-Demerdash, E. (2014). Chrysin alleviates acute doxorubicin cardiotoxicity in rats via suppression of oxidative stress, inflammation and apoptosis. European Journal of Pharmacology, 728, 107–118.
21. Moce, E., Grasseau, I., & Blesbois, E. (2010). Cryoprotectant and freezing-process alter the ability of chicken sperm to acrosome react. Animal Reproduction Science, 122, 359–366.
22. Moghbeli, M., Kohram, H., Zare-Shahaneh, A., Zhandi, M., Sharafi, M., Nabi, M. M., … Sharideh, H. (2016). Are the optimum levels of the catalase and vitamin E in rooster semen extender after freezing-thawing influenced by sperm concentration? Cryobiology, 72, 264–268.
23. Mphaphathi, M. L., Seshoka, M. M., Luseba, D., Sutherland, B., & Nedambale, T. L. (2016). The characterisation and cryopreservation of Venda chicken semen. Asian Pacific Journal of Reproduction, 5, 132–139.
24. Nabi, M. M., Kohram, H., Zhandi, M., Mehrabani-Yeganeh, H., Sharideh, H., Zare-Shahaneh, A., & Esmaili, V. (2016). Comparative evaluation of Nabi and Beltsville extenders for cryopreservation of rooster semen. Cryobiology, 72, 47–52.
25. Neild, D. M., Brouwers, J. F., Colenbrander, B., Aguero, A., & Gadella, B. M. (2005). Lipid peroxide formation in relation to membrane stability of fresh and frozen thawed stallion spermatozoa. Molecular Reproduction and Development, 72, 230–238.
26. Nijveldt, R. J., van Nood, E., van Hoorn, D. E., Boelens, P. G., van Norren, K., & van Leeuwen, P. A. (2001). Flavonoids: A review of probable mechanisms of action and potential applications. American Journal of Clinical Nutrition, 74, 418–425.
27. Pamplona, R. (2008). Membrane phospholipids, lipoxidative damage and molecular integrity: A causal role in aging and longevity. Biochimica et Biophysica Acta, 1777, 1249–1262.
28. Partyka, A., Lukaszewicz, E., & Niżanski, W. (2012). Effect of cryopreservation on sperm parameters, lipid peroxidation and antioxidant enzymes activity in fowl semen. Theriogenology, 77, 1497–1504.
29. Partyka, A., Lukaszewicz, E., Niżanski, W., & Twardon, J. (2011). Detection of lipid peroxidation in frozen-thawed avian spermatozoa using C 11-BODIPY 581/591. Theriogenology, 75, 1623–1629.
30. Pecivova, J., Macickova, T., Svitekova, K., & Nosal, R. (2012). Quercetin inhibits degranulation and superoxide generation in PMA stimulated neutrophils. Interdisciplinary Toxicology, 5, 81–83.
31. Phillips, J. J., Bramwell, R. K., & Graham, J. K. (1996). Cryopreservation of rooster sperm using methyl cellulose. Poultry Science, 75, 915–923.
32. Polge, C. (1951). Functional survival of fowl spermatozoa after freezing at -79°C. Nature, 167, 949–950.
33. Purdy, P. H., Song, Y., Silversides, F. G., & Blackburn, H. D. (2009). Evaluation of glycerol removal techniques, cryoprotectants, and insemination methods for cryopreserving rooster sperm with implications of regeneration of breed or line or both. Poultry Science, 88, 2184–2191.
34. Rengaraj, D., & Hong, Y. (2015). Effects of dietary vitamin E on fertility functions in poultry species. International Journal of Molecular Sciences, 16, 9910–9921.
35. Ross, C., Morriss, A., Khairy, M., Khalaf, Y., Braude, P., Coomarasamy, A., & El-Toukhy, T. (2010). A systematic review of the effect of oral antioxidants on male infertility. Reproductive Biomedicine Online, 20, 711–723.
36. Santiago-Moreno, J., Castano, C., Toledano-Diaz, A., Coloma, M. A., Lopez-Sebastian, A., Prieto, M. T., & Campo, J. L. (2011). Semen cryopreservation for the creation of a Spanish poultry breeds cryobank: Optimization of freezing rate and equilibration time. Poultry Science, 90, 2047–2053.
37. Shahverdi, A., Sharafi, M., Gourabi, H., Yekta, A. A., Esmaeili, V., Sharbatoghli, M., … Mostafayi, F. (2015). Fertility and flow cytometric evaluations of frozen-thawed rooster semen in cryopreservation medium containing low-density lipoprotein. Theriogenology, 83, 78–85.
38. Triques, G. E., Schmidt, J. M., Oro, C. S., Bordignon, H. F., Donin, D. G., & Fernandes, J. I. M. (2016). Effect of dietary antioxidant supplementation on reproductive characteristics of male broiler breeders during the post-peak production phase. Semina: Ciências Agrárias, 37, 2557–2566.
39. Watson, P. F. (2000). The causes of reduced fertility with cryopreserved semen. Animal Reproduction Science, 60–61, 481–491.
40. Zini, A., San Gabriel, M., & Baazeem, A. (2009). Antioxidants and sperm DNA damage: A clinical perspective. Journal of Assisted Reproduction and Genetics, 26, 427–432.