Hyaluronic acid improves frozen-thawed sperm quality and fertility potential in rooster

Animal Reproduction Science

Volumn 184, Issue , 2017, Pages 204-210

  Lotfi, Saied ^a   Mehri, Morteza ^a   Sharafi, Mohsen ^b   Masoudi, Reza ^c  

^a ISLAMIC AZAD UNIVERSITY   (Iran)

^b TARBIAT MODARES UNIVERSITY   (Iran)

^c UNIVERSITY OF TEHRAN   (Iran)

Author keywords

Cryopreservation; Hyaluronic acid (HA); Rooster; Sperm parameters

Indexed keywords

CRYOPROTECTIVE AGENT; HYALURONIC ACID;

ANIMAL; CHICKEN; CRYOPRESERVATION; DRUG EFFECT; FERTILITY; FREEZING; MALE; PHYSIOLOGY; SPERM; SPERMATOZOON; VETERINARY;

ANIMALS; CHICKENS; CRYOPRESERVATION; CRYOPROTECTIVE AGENTS; FERTILITY; FREEZING; HYALURONIC ACID; MALE; SEMEN; SPERMATOZOA;

EID: 85027893243     PISSN: 03784320     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.anireprosci.2017.07.018     Document Type: Article

References (48)

1. Agarwal, A., Virk, G., Ong, C., du Plessis, S.S., Effect of oxidative stress on male reproduction. World J. Men's Health 32 (2014), 1–17.
2. Aitken, J., Fisher, H., Reactive oxygen species generation and human spermatozoa: the balance of benefit and risk. Bioessays 16 (1994), 259–267.
3. Aitken, R.J., Smith, T.B., Jobling, M.S., Baker, M.A., De Iuliis, G.N., Oxidative stress and male reproductive health. Asian J. Andro., 16, 2014, 31.
4. Amini, M.R., Kohram, H., Shahaneh, A.Z., Zhandi, M., Sharideh, H., Nabi, M.M., 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 (2015), 587–592.
5. Anzar, M., He, L., Buhr, M.M., Kroetsch, T.G., Pauls, K.P., Sperm apoptosis in fresh and cryopreserved bull semen detected by flow cytometry and its relationship with fertility. Biol. Reprod. 66 (2002), 354–360.
6. Bansal, A.K., Antioxidants and other potent strategies to reduce oxidative stress in semen. Free Radicals in Human Health and Disease, 2015, Springer, India, 381–395.
7. Barreto, R.B., Sadigursky, D., Rezende, M.U.D., Hernandez, A.J., Effect of hyaluronic acid on chondrocyte apoptosis. Act. Ortoped. Brasil 23 (2015), 90–93.
8. Baumber, Julie, Ball, B.A., Gravance, C.G., Medina, Victor, Davies-Morel, M.C., The effect of reactive oxygen species on equine sperm motility, viability, acrosomal integrity, mitochondrial membrane potential and membrane lipid peroxidation. J. Andro. 21 (2000), 895–902.
9. Braga, P.C., Dal Sasso, M., Lattuada, N., Greco, V., Sibilia, V., Zucca, E., Stucchi, L., Ferro, E., Ferrucci, F., Antioxidant activity of hyaluronic acid investigated by means of chemiluminescence of equine neutrophil bursts and electron paramagnetic resonance spectroscopy. J. Vet. Pharmaco. Therap. 38 (2015), 48–54.
10. Bucak, M.N., Ateşşahin, A., Varışlı, Ö., Yüce, A., Tekin, N., Akçay, A., The influence of trehalose, taurine, cysteamine and hyaluronan on ram semen: microscopic and oxidative stress parameters after freeze-thawing process. Theriogenology 67 (2007), 1060–1067.
11. Bucak, M.N., Sarıözkan, S., Tuncer, P.B., Ulutaş, P.A., Akçadağ, H.İ., Effect of antioxidants on microscopic semen parameters, lipid peroxidation and antioxidant activities in Angora goat semen following cryopreservation. Small Rumin. Res. 81 (2009), 90–95.
12. Burrows, W.H., Quinn, J.P., The collection of spermatozoa from the domestic fowl and turkey. Poult. Sci. 16 (1937), 19–24.
13. Chalah, T., Seigneurin, F., Blesbois, E., Brillard, J.P., In vitro comparison of fowl sperm viability in ejaculates frozen by three different techniques and relationship with subsequent fertility in vivo. Cryobiology 39 (1999), 185–191.
14. Chenoweth, P.J., Genetic sperm defects. Theriogenology 64 (2005), 457–468.
15. Eidan, S.M., Effect on post-cryopreserved semen characteristics of Holstein bulls of adding combinations of vitamin C and either catalase or reduced glutathione to Tris extender. Anim. Reprod. Sci. 167 (2016), 1–7.
16. El-Sheshtawy, R.I., Sisy, G.A., El-Nattat, W.S., Effects of different concentrations of sucrose or trehalose on the post-thawing quality of cattle bull semen. Asian Pacif. J. Reprod. 4 (2015), 26–31.
17. Emamverdi, M., Zhandi, M., Shahneh, A.Z., Sharafi, M., Akhlaghi, A., Motlagh, M.K., Dadkhah, F., Davachi, N.D., Flow cytometric and microscopic evaluation of post-thawed ram semen cryopreserved in chemically defined home-made or commercial extenders. Anim. Prod. Sci. 55 (2015), 551–558.
18. Esmaeili, V., Shahverdi, A.H., Moghadasian, M.H., Alizadeh, A.R., Dietary fatty acids affect semen quality: a review. Andrology 3 (2015), 450–461.
19. Fattah, A., Sharafi, M., Masoudi, R., Shahverdi, A., Esmaeili, V., Najafi, A., l-Carnitine in rooster semen cryopreservation: flow cytometric, biochemical and motion findings for frozen-thawed sperm. Cryobiology 74 (2017), 148–153.
20. Fattah, A., Sharafi, M., Masoudi, R., Shahverdi, A., Esmaeili, V., L-carnitine is a survival factor for chilled storage of rooster semen for a long time. Cryobiology 74 (2017), 13–18.
21. Ghosh, I., Bharadwaj, A., Datta, K., Reduction in the level of hyaluronan binding protein 1 (HABP1) is associated with loss of sperm motility. J. Reproduct. Immun. 53 (2002), 45–54.
22. Grishko, V., Xu, M., Ho, R., Mates, A., Watson, S., Kim, J.T., Wilson, G.L., Pearsall, A.W., Effects of hyaluronic acid on mitochondrial function and mitochondria-driven apoptosis following oxidative stress in human chondrocytes. J. Biol. Chemist. 284 (2009), 9132–9139.
23. Grossfeld, R., Sieg, B., Struckmann, C., Frenzel, A., Maxwell, W.M.C., Rath, D., New aspects of boar semen freezing strategies. Theriogenology 70 (2008), 1225–1233.
24. Huszar, G., Willetts, M., Corrales, M., Hyaluronic acid (Sperm Select) improves retention of sperm motility and velocity in normospermic and oligospermic specimens. Fertil. Steril. 54 (1990), 1127–1134.
25. Long, J.A., Avian semen cryopreservation: what are the biological challenges?. Poult. Sci. 85 (2006), 232–236.
26. Masoudi, R., Sharafi, M., Shahneh, A.Z., Towhidi, A., Kohram, H., Esmaeili, V., Shahverdi, A., Davachi, N.D., Fertility and flow cytometry study of frozen-thawed sperm in cryopreservation medium supplemented with soybean lecithin. Cryobiology 73 (2016), 69–72.
27. Masoudi, R., Sharafi, M., Shahneh, A.Z., Towhidi, A., Kohram, H., Zhandi, M., Esmaeili, V., Shahverdi, A., Effect of dietary fish oil supplementation on ram semen freeze ability and fertility using soybean lecithin–and egg yolk–based extenders. Theriogenology 86 (2016), 1583–1588.
28. Masoudi, R., Shahneh, A.Z., Towhidi, A., Kohram, H., Akbarisharif, A., Sharafi, M., Fertility response of artificial insemination methods in sheep with fresh and frozen-thawed semen. Cryobiology 74 (2017), 77–80.
29. Mendoza, Gracia, Prieto, J.G., Real, R., Perez, Miriam, Merino, Gracia, Alvarez, A.I., Antioxidant profile of hyaluronan: physico-Chemical features and its role in pathologies. Mini-Rev. Med. Chem. 9 (2009), 1479–1488.
30. Nabi, M.M., Kohram, H., Zhandi, M., Mehrabani-Yeganeh, H., Sharideh, H., Zare-Shahaneh, A., Esmaili, V., Comparative evaluation of Nabi and Beltsville extenders for cryopreservation of rooster semen. Cryobiology 72 (2016), 47–52.
31. Najafi, A., Najafi, M.H., Zanganeh, Z., Sharafi, M., Martinez‐Pastor, F., Adeldust, H., Cryopreservation of ram semen in extenders containing soybean lecithin as cryoprotectant and hyaluronic acid as antioxidant. Reprod. Domest. Anim. 49 (2014), 934–940.
32. Necas, J., Bartosikova, L., Brauner, P., Kolar, J., Hyaluronic acid (hyaluronan): a review. Vet. Med. 53 (2008), 397–411.
33. Parks, J.E., Lynch, D.V., Lipid composition and thermotropic phase behavior of boar, bull, stallion, and rooster sperm membranes. Cryobiology 29 (1992), 255–266.
34. Pena, F.J., Johannisson, A., Wallgren, M., Rodriguez-Martinez, H., Effect of hyaluronan supplementation on boar sperm motility and membrane lipid architecture status after cryopreservation. Theriogenology 61 (2004), 63–70.
35. Qian, L., Yu, S., Zhou, Y., Protective effect of hyaluronic acid on cryopreserved boar sperm. In. J. Biolog. Macromolecul. 87 (2016), 287–289.
36. Ranganathan, S., Ganguly, A.K., Datta, K., Evidence for presence of hyaluronan binding protein on spermatozoa and its possible involvement in sperm function. Mol. Reprod. Develop. 38 (1994), 69–76.
37. Salmani, H., Nabi, M.M., Vaseghi-Dodaran, H., Rahman, M.B., Mohammadi-Sangcheshmeh, A., Shakeri, M., Towhidi, A., Shahneh, A.Z., Zhandi, M., Effect of glutathione in soybean lecithin-based semen extender on goat semen quality after freeze-thawing. Small Rumin. Res. 112 (2013), 123–127.
38. Sarıözkan, S., Bucak, M.N., Tuncer, P.B., Büyükleblebici, S., Eken, A., Akay, C., Influence of fetuin and hyaluronan on the post-thaw quality and fertilizing ability of Holstein bull semen. Cryobiology 71 (2015), 119–124.
39. Sbracia, M., Grasso, J., Sayme, N., Stronk, J., Huszar, G., Hyaluronic acid substantially increases the retention of motility in cryopreserved/thawed human spermatozoa. Hum. Reprod. 12 (1997), 1949–1954.
40. Schäfer, S., Holzmann, A., The use of transmigration and Spermac™ stain to evaluate epididymal cat spermatozoa. Anim. Reprod. Sci. 59 (2000), 201–211.
41. Schnitzer, E., Dagan, A., Krimsky, M., Lichtenberg, D., Pinchuk, I., Shinar, H., Yedgar, S., Interaction of hyaluronic acid-linked phosphatidylethanolamine (HyPE) with LDL and its effect on the susceptibility of LDL lipids to oxidation. Chemist. Physic. Lipid. 104 (2000), 149–160.
42. Shahverdi, A., Sharafi, M., Gourabi, H., Yekta, A.A., Esmaeili, V., Sharbatoghli, M., Janzamin, E., Hajnasrollahi, M., Mostafayi, F., Fertility and flow cytometric evaluations of frozen-thawed rooster semen in cryopreservation medium containing low-density lipoprotein. Theriogenology 83 (2015), 78–85.
43. Sharafi, M., Zhandi, M., Akbari Sharif, A., Supplementation of soybean lecithin-based semen extender by antioxidants: complementary flowcytometric study on post-thawed ram spermatozoa. Cell Tissue Bank. 16 (2015), 261–269.
44. Sharafi, M., Zhandi, M., Shahverdi, A., Shakeri, M., Beneficial effects of nitric oxide induced mild oxidative stress on post-thawed bull semen quality. In. J. Fertil. Ster. 9 (2015), 230–237.
45. Simulescu, V., Kalina, M., Mondek, J., Pekař, M., Long-term degradation study of hyaluronic acid in aqueous solutions without protection against microorganisms. Carbohydr. Polym. 137 (2016), 664–668.
46. Singh, A., Li, P., Beachley, V., McDonnell, P., Elisseeff, J.H., A hyaluronic acid-binding contact lens with enhanced water retention. Contact Lens Anterior Eye 38 (2015), 79–84.
47. Suzuki, K., Asano, A., Eriksson, B., Niwa, K., Nagai, T., Rodriguez-Martinez, H., Capacitation status and in vitro fertility of boar spermatozoa: effects of seminal plasma, cumulus-oocyte-complexes-conditioned medium and hyaluronan. In. J. Andro. 25 (2002), 84–93.
48. Tokita, Y., Sakashita, H., Okamoto, A., Kubota, K., Kinetic study of a radical scavenging effect of hyaluronic acid. Polym. In. 38 (1995), 161–164.