Zinc Oxide Nanoparticles Have Beneficial Effect on Frozen-Thawed Spermatozoa of Holstein Bulls
Subject Areas : CamelF. Farhadi 1 , A. Towhidi 2 , M. Shakeri 3 , A. Seifi-Jamadi 4
1 - Department of Animal Science, College of Agriculture and Natural Resources, University of Tehran, Karaj, Iran
2 - Department of Animal Science, College of Agriculture and Natural Resources, University of Tehran, Karaj, Iran
3 - Department of Animal Science, College of Agriculture and Natural Resources, University of Tehran, Karaj, Iran
4 - Department of Animal Science, College of Agriculture and Natural Resources, University of Tehran, Karaj, Iran
Keywords:
Abstract :
Afifi M., Almaghrabi O.A. and Kadasa N.M. (2015). Ameliorative effect of zinc oxid nanoparticles on antioxidants and sperm characteristics in streptozotocin-induced diabetic rat testes. BioMed. Res. Int. 2015, 1-6.
Aitken R.J. (2018). Not every sperm is sacred; a perspective on male infertility. MHR Basic Sci. Reprod. Med. 24, 287-298.
Aitken R.J., Gibb Z., Baker M.A., Drevet J. and Gharagozloo P. (2016). Causes and consequences of oxidative stress in spermatozoa. Reprod. Fertil. Dev. 28, 1-10.
Amini M.R., Kohram H, Shahaneh A.Z., Zhandi M, Sharideh H. and Nabi M.M. (2015). 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.
Baccetti B., Pallini V. and Burrini A. (1973). The accessory fibers of the sperm tail. I. Structure and chemical composition of the bull coarse fibers. J. Submicrosc. Cytol. 5, 237-256.
Barkhordari A., Hekmatimoghaddam S., Jebali A, Khalili M.A., Talebi A. and Noorani M. (2013). Effect of zinc oxide nanoparticles on viability of human spermatozoa. Int. J. Reprod. Biomed. 11, 767-771.
Björndahl L., Söderlund I. and Kvist U. (2003). Evaluation of the one step eosin nigrosin staining technique for human sperm vitality assessment. Hum. Reprod. 18, 813-816.
Bray T.M. and Bettger W.J. (1990). The physiological role of zinc as an antioxidant. Free Radical Biol. Med. 8, 281-291.
Bülbül B., Akalin P.P., Başpinar N., Bucak M.N., Kirbaş M., Öztürk C., Güngör Ş. and Akbulut K. (2019). A comparative study of seminal plasma and blood serum macro and trace elements in the the breeding (October) and the non-breeding (April) seasons in Merino ram. J. Hellenic Vet. Med. Soc. 70(1), 1365-1372.
Chohan K., Griffin J. and Carrell D. (2004). Evaluation of chromatin integrity in human sperm using acridine orange staining with different fixatives and after cryopreservation. Andrologia. 36, 321-326.
Colagar A.H., Marzony E.T. and Chaichi M.J. (2009). Zinc levels in seminal plasma are associated with sperm quality in fertile and infertile men. Nutri. Res. 29, 82-88.
Cummings J.E. and Kovacic J.P. (2009). The ubiquitous role of zinc in health and disease. J. Vet. Emerg. Crit. Care. 19(3), 215-240.
Dawei A., Zhisheng W. and Anguo Z. (2010). Protective effects of nano-ZnO on the primary culture mice intestinal epithelial cells in in vitro against oxidative injury. J. Anim. Vet. Adv. 6, 149-153.
Eidan S.M. (2016). 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, 1-7.
Evans G. and Maxwell W.C. (1987). Salamons' Artificial Insemination of Sheep and Goats. Butterworths, Axfordshire, United Kingdom.
Gualtieri R., Barbato V., Fiorentino I., Braun S., Rizos D., Longobardi S. and Talevi R. (2014). Treatment with zinc, d-aspartate, and coenzyme Q10 protects bull sperm against damage and improves their ability to support embryo development. Theriogenology. 82(4), 592-598.
Hammadeh M.E., Filippos A. and Hamad M.F. (2009). Reactive oxygen species and antioxidant in seminal plasma and their impact on male fertility. Int. J. Fertil. Steril. 3, 87-110.
Hedayat-Evrigh N., Moradi F., Vahedi V., Navidshad B. and Seifi-Jamadi A. (2019). Influence of various dietary fat sources on freezing capacity of Moghani ram semen. South African J. Anim. Sci. 49(3), 505-512.
Hidiroglou M. and Knipfel J. (1984). Zinc in mammalian sperm: A review. J. Dairy Sci. 67, 1147-1156.
Isaac A.V., Kumari S., Nair R., Urs D.R., Salian S.R., Kalthur G., Adiga S.K., Manikhath J., Mutalik S. and Pasricha R. (2017). Supplementing zinc oxide nanoparticles to cryopreservation medium minimizes the freeze-thaw-induced damage to spermatozoa. Biochem. Biophys. Res. Commun. 494(3), 656-662.
Kadirvel G., Kumar S. and Kumaresan A. (2009). Lipid peroxidation, mitochondrial membrane potential and DNA integrity of spermatozoa in relation to intracellular reactive oxygen species in liquid and frozen-thawed buffalo semen. Anim. Reprod. Sci. 114, 125-134.
Karimi R., Towhidi A., Zeinoaldini S., Rezayazdi K., Mousavi M., Safari H. and Martinez Pastor F. (2017). Effects of supplemental conjugated linoleic acids (CLA) on fresh and post thaw sperm quality of Holstein bulls. Reprod. Domest. Anim. 52, 459-467.
Kellokumpu S. and Rajaniemi H. (1981). Effect of zinc on the uptake of human chorionic gonadotropin (hCG) in rat testis and testosterone response in vivo. Biol. Reprod. 24, 298-305.
Khoobbakht Z., Mohammadi M., Mehr M.R.A., Mohammadghasemi F. and Sohani M.M. (2018). Comparative effects of zinc oxide, zinc oxide nanoparticle and zinc-methionine on hatchability and reproductive variables in male Japanese quail. Anim. Reprod. Sci. 192, 84-90.
Kotdawala A.P., Kumar S., Salian S.R., Thankachan P., Govindraj K., Kumar P., Guruprasad K. and Adiga S.K. (2012). Addition of zinc to human ejaculate prior to cryopreservation prevents freeze-thaw-induced DNA damage and preserves sperm function. J. Assist. Reprod. Gen. 29, 1447-1453.
Kvist U., Björndahl L. and Kjellberg S. (1987). Sperm nuclear zinc, chromatin stability, and male fertility. Scanning. Microsc. 1, 12-41.
Liu Q., Xu C., Ji G., Liu H., Mo Y., Tollerud D.J., Gu A. and Zhang Q. (2016). Sublethal effects of zinc oxide nanoparticles on male reproductive cells. Toxicol. In Vitro. 35, 131-138.
Medeiros C., Forell F., Oliveira A. and Rodrigues J. (2002). Current status of sperm cryopreservation: why isn't it better? Theriogenology. 57, 327-344.
Mohamed D.A. and Abdelrahman S.A. (2018). The possible protective role of zinc oxide nanoparticles (ZnONPs) on testicular and epididymal structure and sperm parameters in nicotine-treated adult rats (a histological and biochemical study). Cell Tissue Res. 375, 543-558.
Mousavi S.M., Towhidi A., Zhandi M., Amoabediny G., Mohammadi-Sangcheshmeh A., Sharafi M. and Hussaini S. M.H. (2019). Comparison of two different antioxidants in a nano lecithin-based extender for bull sperm cryopreservation. Anim. Reprod. Sci. 209, 106171-10679.
Narasimhaiah M., Arunachalam A., Sellappan S., Mayasula V. K., Guvvala P.R., Ghosh S.K. and Kumar H. (2018). Organic zinc and copper supplementation on antioxidant protective mechanism and their correlation with sperm functional characteristics in goats. Reprod. Domest. Anim. 53(3), 644-654.
Omu A.E., Al-Azemi M.K., Kehinde E.O., Anim J.T., Oriowo M.A. and Mathew T.C. (2008). Indications of the mechanisms involved in improved sperm parameters by zinc therapy. Med. Princ. Pract. 17(2), 108-116.
Prasad A.S. (2009). Zinc: Role in immunity, oxidative stress and chronic inflammation. Curr. Opin. Clin. Nutr. Metab. Care. 12(6), 646-652.
Rahmatzadeh M., Kohram H., Zare Shahneh A., Seifi Jamadi A. and Ahmad E. (2017). Antioxidative effect of BHA in soya bean lecithin based extender containing glycerol or DMSO on freezing capacity of goat semen. Reprod. Domest. Anim. 52(6), 985-991.
Revell S. and Mrode R. (1994). An osmotic resistance test for bovine semen. Anim. Reprod. Sci. 36, 77-86.
Root A.W., Duckett G., Sweetland M. and Reiter E.O. (1979). Effects of zinc deficiency upon pituitary function in sexually mature and immature male rats. J. Nutr. 109, 9-58.
SAS Institute. (2003). SAS®/STAT Software, Release 9.1. SAS Institute, Inc., Cary, NC. USA.
Schäfer S. and Holzmann A. (2000). The use of transmigration and Spermac™ stain to evaluate epididymal cat spermatozoa. Anim. Reprod. Sci. 59, 201-211.
Seifi-Jamadi A., Ahmad E., Ansari M. and Kohram H. (2017). Antioxidant effect of quercetin in an extender containing DMA or glycerol on freezing capacity of goat semen. Cryobiology. 75, 15-20.
Seifi-Jamadi A., Kohram H., Zareh-Shahne A., Dehghanizadeh P. and Ahmad E. (2016). Effect of various concentrations of butylated hydroxyanisole and butylated hydroxytoluene on freezing capacity of Turkman stallion sperm. Anim. Reprod. Sci. 170, 108-113.
Sørensen M.B., Stoltenberg M., Danscher G. and Ernst E. (1999). Chelation of intracellular zinc ions affects human sperm cell motility. Mol. Hum. Rep. 5(4), 338-341.
Surai P., Blesbois E., Grasseau I., Chalah T., Brillard J.P., Wishart G., Cerolini S. and Sparks N. (1998). Fatty acid composition, glutathione peroxidase and superoxide dismutase activity and total antioxidant activity of avian semen. Comp. Biochem. Physiol. B Biochem. Mol. Biol. 120, 527-533.
Talebi A.R., Khorsandi L. and Moridian M. (2013). The effect of zinc oxide nanoparticles on mouse spermatogenesis. J. Assist. Reprod. Gen. 30, 1203-1209.
Thys M., Nauwynck H., Maes D., Hoogewijs M., Vercauteren D., Rijsselaere T., Favoreel H. and Van Soom A. (2009). Expression and putative function of fibronectin and its receptor (integrin α5β1) in male and female gametes during bovine fertilization in vitro. Reproduction. 138, 471-482.
Topraggaleh T., Shahverdi A., Rastegarnia A., Ebrahimi B., Shafiepour V., Sharbatoghli M., Esmaeili V. and Janzamin E. (2014). Effect of cysteine and glutamine added to extender on post thaw sperm functional parameters of buffalo bull. Andrologia. 46, 777-783.
Vafaei F., Kohram H., Zareh-Shahne A., Ahmad E. and Seifi-Jamadi A. (2019). Influence of different combinations of permeable and nonpermeable cryoprotectants on the freezing capacity of equine sperm. J. Equine Vet. Sci. 75, 69-73.
Vishwanath R. and Shannon P. (2000). Storage of bovine semen in liquid and frozen state. Anim. Reprod. Sci. 62, 23-53.
Zago M.P. and Oteiza P.I. (2001). The antioxidant properties of zinc: interactions with iron and antioxidants. Free Radic. Biol. Med. 31, 266-274.
Zanganeh Z., Zhandi M., Zare-Shahneh A., Najafi A., Nabi M.M. and Mohammadi-Sangcheshmeh A. (2013). Does rosemary aqueous extract improve buck semen cryopreservation? Small Rumin. Res. 114, 120-125.
Zhandi M., Seifi-Ghajalo E., Shakeri M., Yousefi A.R., Sharafi M. and Seifi-Jamadi A. (2020). Effect of glutathione supplementation to semen extender on post-thawed rooster sperm quality indices frozen after different equilibration times. CryoLetters. 41, 92-99.
Zhandi M., Talebnia-Chalanbar A., Towhidi A., Sharafi M., Yousefi A.R. and Hussaini S.M.H. (2019). The effect of zinc oxide on rooster semen cryopreservation. British Poult. Sci. 61, 188-194.
