The role of environmental optimization for storing bulls’ sperm cells

References

• Adami LNG, Belardin LB, Lima BT, Jeremias JT, Antoniassi MP, Okada FK, Bertolla RP. 2018 May. Effect of in vitro vitamin E (alpha‐tocopherol) supplementation in human spermatozoon submitted to oxidative stress. Andrologia. 50(4):e12959. doi:10.1111/and.12959.
   Web of Science ®Google Scholar
• Agarwal A, Said TM, Bedaiwy MA, Banerjee J, Alvarez JG. 2006. Oxidative stress in an assisted reproductive techniques setting. Fertil Steril. 86:503–512. doi:10.1016/j.fertnstert.2006.02.088.
   PubMed Web of Science ®Google Scholar
• Aitken RJ. 1995. Free radicals, lipid peroxidation and sperm function. Reprod Fertil Dev. 7(4):659–668. doi:10.1071/RD9950659.
   PubMed Web of Science ®Google Scholar
• Aitken RJ, De Iuliis GN, McLachlan RI. 2009. Biological and clinical significance of DNA damage in the male germ line. Int J Androl. 32(1):46–56. doi:10.1111/j.1365-2605.2008.00943.x.
   PubMedGoogle Scholar
• Allai L, Benmoula A, Marciane da Silva M, Nasser B, El Amiri B. 2018. Supplementation of ram semen extender to improve seminal quality and fertility rate. Anim Reprod Sci. 192:6–17. doi:10.1016/j.anireprosci.2018.03.019.
   PubMed Web of Science ®Google Scholar
• Alvarez C, Castilla JA, Ramirez JP, Vergara F, Yoldi A, Fernandez A. 2005. External quality control program for semen analysis: spanish experience. J Assist Reprod Genet. 22:379–387. doi:10.1007/s10815-005-7461-2.
   PubMed Web of Science ®Google Scholar
• Amann RP, Graham JK. 1993. Spermatozoal function. Equine reproduction. Philadelphia (PA): Lea and Febiger; p. 715–745.
   Google Scholar
• Anderson J. 1945. The semen of animals and its use for artificial insemination. Tech Commun Imp Bur Anim Breed Genet London. 6:151.
   Google Scholar
• Atmaca G. 2004. Antioxidant effects of sulfur-containing amino acids. Yonsei Med J. 45:776–788. doi:10.3349/ymj.2004.45.5.776.
   PubMed Web of Science ®Google Scholar
• Bailey JL, Bilodeau JF, Cormier N. 2000. Semen cryopreservation in domestic animals: A damaging and capacitating phenomenon. J Androl. 21:1–7.
   PubMedGoogle Scholar
• Bailey JL, Lessard C, Jacques J, Bre`que C, Dobrinski I, Zeng W, GalantinoHomer HL. 2008. Cryopreservation of boar semen and its future importance to the industry. Theriogenology. 70:1251–1259. doi:10.1016/j.theriogenology.2008.06.014.
   PubMed Web of Science ®Google Scholar
• Ball BA. 2008. Oxidative stress, osmotic stress and apoptosis: impacts on sperm function and preservation in the horse. Anim Reprod Sci. 107:257–267. doi:10.1016/j.anireprosci.2008.04.014.
   PubMed Web of Science ®Google Scholar
• Barbas JP, Mascarenhas RD. 2009. Cryopreservation of domestic animal sperm cells. Cell Tissue Bank. 10:49–62. doi:10.1007/s10561-008-9081-4.
   PubMed Web of Science ®Google Scholar
• Bartlett FD, Van Demark NL. 1962. Effect of diluent composition on survival and fertility of bovine spermatozoa stored in carbonated diluents. J Dairy Sci. 45:360–367. doi:10.3168/jds.S0022-0302(62)89399-0.
   Web of Science ®Google Scholar
• Bilodeau J-F, Chatterjee S, Sirard MA, Gagnon C. 2000. Levels of antioxidant defenses are decreased in bovine spermatozoa after a cycle of freezing. Mol Hum Reprod. 55:282–288. doi:10.1002/(SICI)1098-2795(200003)55:3<282::AID-MRD6>3.0.CO;2-7.
   Google Scholar
• Blackshaw AW. 1954. The prevention of temperature shock of bull and ram spermatozoa. Aust J Biol Sci. 7:573–582. doi:10.1071/BI9540573.
   PubMedGoogle Scholar
• Bollwein H, Fuchs I, Koess C. 2008. Interrelationship between plasma membrane integrity, mitochondrial membranę potential and DNA fragmentation in cryopreserved bovine spermatozoa. Reprod Domest Anim. 43:189–195. doi:10.1111/j.1439-0531.2007.00876.x.
   PubMed Web of Science ®Google Scholar
• Brito LFC. 2016. A multilaboratory study on the variability of bovine semen analysis. Theriogenology. 85:254–266. doi:10.1016/j.theriogenology.2015.05.027.
   PubMed Web of Science ®Google Scholar
• Celeghini EC, Arruda RP, Cesarde AF, Nascimento AJ, Fernandes C, Paulo R, Rodrigues HM. 2008. Effects that bovine sperm cryopreservation using two different extenders has on sperm membranes and chromatin. Anim Reprod Sci. 104(2–4):119–131. doi:10.1016/j.anireprosci.2007.02.001.
   PubMed Web of Science ®Google Scholar
• Cerolini S, Maldjian A, Pizzi F, Gliozzi TM. 2001. Changes in sperm quality and lipid composition during cryopreservation of boar semen. Reproduction. 121:395–401. doi:10.1530/rep.0.1210395.
   PubMed Web of Science ®Google Scholar
• Chatterjee S, De Lamirande E, Gagnon C. 2001. Cryopreservation alters membrane sulfhydryl status of bull spermatozoa: protection by oxidized glutathione. Mol Reprod Dev. 60:498–506. doi:10.1002/mrd.1115.
   PubMed Web of Science ®Google Scholar
• Chuawongboon P, Sirisathien S, Pongpeng J, Sakhong D, Nagai T, Vongpralub T. 2017. Effects of supplementation of iodixanol to semen extender on quality and fertilization ability of frozen–thawed Thai native bull sperm. Animal. 88(9):1311–1320.
   Web of Science ®Google Scholar
• Collins JA, Barnhart KT, Schlegel PN. 2008. Do sperm DNA integrity tests predict pregnancy with in vitro fertilization? Fertil Steril. 89(4):823–831. doi:10.1016/j.fertnstert.2007.04.055.
   PubMed Web of Science ®Google Scholar
• Coyan K, Baspınar N, Bucak MN, Akahn PP. 2011. Effects of cysteine and ergothioneine on post-thawed Merino ram sperm and biochemical parameters. Cryobiology. 63:1–6. doi:10.1016/j.cryobiol.2011.04.001.
   PubMed Web of Science ®Google Scholar
• Daghigh-Kia H, Olfati-Karaji R, Hoseinkhani A, Ashrafi I. 2014. Effect of rosemary (Rosmarinus officinalis) extracts and glutathione antioxidants on bull semen quality after cryopreservation. Spanish J Agric Res. 12(1):12–19.
   Web of Science ®Google Scholar
• Darin-Bennett A, White IG. 1977. Influence of the cholesterol content of mammalian spermatozoa on susceptibility to cold-shock. Cryobiology. 14:466–470. doi:10.1016/0011-2240(77)90008-6.
   PubMed Web of Science ®Google Scholar
• Davis IS, Bratton RW, Foote RH. 1963a. Livability of bovine spermatozoa at 5, −25 and −85°C in tris-buffered and citrate-buffered yolk-glycerol extenders. J Dairy Sei. 46:333–336. doi:10.3168/jds.S0022-0302(63)89041-4.
   Web of Science ®Google Scholar
• Davis IS, Bratton RW, Foote RH. 1963b. Livability of bovine spermatozoa at 5°C in tris-buffered and citrate-buffered yolk-glycerol extenders. J Dairy Sei. 46:57–60. doi:10.3168/jds.S0022-0302(63)88964-X.
   Web of Science ®Google Scholar
• De Leeuw FE, De Leeuw AM, Den Daas JHG, Colenbrander B, Verkleij AJ. 1993. Effects of various cryoprotective agents and membranę stabilizing compounds on bull sperm membranę integrity after cooling and freezing. Cryobiology. 30(1):32–44. doi:10.1006/cryo.1993.1005.
   PubMed Web of Science ®Google Scholar
• Dziekonska A, Fraser L, Strezezek J. 2009. Effect of different storage temperatures on the metabolic activity of spermatozoa following liquid storage of boar semen. J Anim Feed Sci. 18:638–649. doi:10.22358/jafs/66438/2009.
   Web of Science ®Google Scholar
• Ezz MA, Montasser AE, Hussein M, Eldesouky A, Badr M, Hegab AE. 2017. The effect of cholesterol loaded cyclodextrins on post-thawing quality of buffalo semen in relation to sperm DNA damage and ultrastructure. Reprod Biol. 17(1):42–50. doi:10.1016/j.repbio.2016.12.001.
   PubMed Web of Science ®Google Scholar
• Fernández-Gonzalez R, Moreira PN, Pérez-Crespo M, Sánchez-Martín M, Ramirez MA, Pericuesta E, Bilbao A, Bermejo-Alvarez P, de Dios Hourcade J, de Fonseca FR, et al. 2008. Long-term effects of mouse intracytoplasmic sperm injection with DNA-fragmented sperm on health and behavior of adult offspring. Biol Reprod. 78(4):761–772. doi:10.1095/biolreprod.107.065623.
   PubMed Web of Science ®Google Scholar
• Fernández-Santos MR, Esteso MC, Montoro V, Soler AJ, Garde JJ. 2006. Cryopreservation of Iberian red deer (Cervus elaphus hispanicus) epididymal spermatozoa: effects of egg yolk, glycerol and cooling rate. Theriogenology. 66:1931–1942. doi:10.1016/j.theriogenology.2006.05.012.
   PubMed Web of Science ®Google Scholar
• Foote RH, Bratton RW. 1960. Survival of bovine spermatozoa stored at 5 and 25°C in extenders containing varying levels of egg yolk, glucose, glycine, glycerol, citrate and other salts. J Dairy Sci. 43:1330–1334. doi:10.3168/jds.S0022-0302(60)90320-9.
   Web of Science ®Google Scholar
• Foote RJ. 1978. Extenders and extension of unfrozen semen. Physiology of reproduction artificial insemination of cattle. San Francisco: Freeman; p. 442–493.
   Google Scholar
• Gadea J, Molla M, Selles E, Marco M, Garcia-Vazquez F, Gardon J. 2011. Reduced glutathione content in human sperm is decreased after cryopreservation: effect of the addition of reduced glutathione to the freezing and thawing extenders. Cryobiology. 62:40–46. doi:10.1016/j.cryobiol.2010.12.001.
   PubMed Web of Science ®Google Scholar
• Ge S, Lin S, Zhao Z, Sun Q. 2017. Epigenetic dynamics and interplay during spermatogenesis and embryogenesis: implications for male fertility and offspring health. Oncotarget. 8:53804–53818. doi:10.18632/oncotarget.17479.
   PubMedGoogle Scholar
• Gebauer MR, Pickett BW, Komarek RJ, Gaunya WS. 1970. Motility of bovine spermatozoa extended in “defined” diluents. J Dairy Sci. 53:817–823. doi:10.3168/jds.S0022-0302(70)86297-X.
   PubMed Web of Science ®Google Scholar
• Gillan L, Maxwell WM, Evans G. 2004. Preservation and evaluation of semen for artificial insemination. Reprod Fertil Dev. 16:447–454. doi:10.1071/RD04034.
   PubMed Web of Science ®Google Scholar
• Good NE, Winget GD, Winter W, Connolly TT, Izawa S, Singh RMM. 1966. Hydrogen ion buffer for biological research. Biochemistry. 5:467–477. doi:10.1021/bi00866a011.
   PubMed Web of Science ®Google Scholar
• Grötter LG, Cattaneo L, Estela P, Kjelland ME, Ferré LB. 2019. Recent advances in bovine sperm cryopreservation techniques with a focus on sperm post—Thaw quality optimization. Reprod Domest Anim. 54:655–665. doi:10.1111/rda.13409.
   PubMed Web of Science ®Google Scholar
• Gürler H, Malama E, Heppelmann M, Calisici O, Leiding C, Kastelic JP, Bollwein H. 2016. Effects of cryopreservation on sperm viability, synthesis of reactive oxygen species, and DNA damage of bovine sperm. Theriogenology. 86:562–571. doi:10.1016/j.theriogenology.2016.02.007.
   PubMed Web of Science ®Google Scholar
• Hawk HW, Conley HH, Cooper BS. 1978. Number of sperm in the oviducts, uterus, and cervix of the mated ewe as affected by exogenous estradiol. J Anim Sci. 46:1300–1308. doi:10.2527/jas1978.4651300x.
   PubMed Web of Science ®Google Scholar
• Ho HC, Granish KA, Suarez SS. 2002. Hyperactivated motility of bull sperm is triggered at the axoneme by ca2+ and not camp. Dev Biol. 250:208–217. doi:10.1006/dbio.2002.0797.
   PubMed Web of Science ®Google Scholar
• Jang H, Kim YH, Kim BW, Park IC, Cheong HT, Kim JT, Park CK, Kong HS, Lee HK, Yang BK. 2010. Ameliorative effects of melatonin against hydrogen peroxide-induced oxidative stress on boar sperm characteristics and subsequent in vitro embryo development. Reprod Domest Anim. 45:943–950. doi:10.1111/j.1439-0531.2009.01466.x.
   PubMed Web of Science ®Google Scholar
• Jeong YJ, Kim M-K, Song H-J, Kang E-J, Ock S-A, Mohana Kumar B, Balasubramanian S, Rho G-J. 2009. Effect of a-tocopherol supplementation during boar semen cryopreservation on sperm characteristics and expression of apoptosis related genes. Cryobiology. 58:181–189. doi:10.1016/j.cryobiol.2008.12.004.
   PubMed Web of Science ®Google Scholar
• Johnson L, Weitze K, Fiser P, Maxwell W. 2000. Storage of boar semen. Anim Reprod Sei. 62:143–172. doi:10.1016/S0378-4320(00)00157-3.
   PubMed Web of Science ®Google Scholar
• Jones RC. 1976. The naturę of ultrastructural changes indusced by exposure of spermatozoa to lysolecithin. Theriogenology. 6:656. doi:10.1016/0093-691X(76)90095-9.
   PubMedGoogle Scholar
• Kadirvel G, Kumar S, 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. doi:10.1016/j.anireprosci.2008.10.002.
   PubMed Web of Science ®Google Scholar
• Kaka A, Wahida H, Rosnina Y, Yimera N, Khumran AM, Sarsaifia K, Behanb AA, Kaka U, Ebrahimi M. 2015. A-Linolenic aeid supplementation in BioXcell® extender can improve the quality of post-cooling and frozen-thawed bovine sperm. Anim Reprod Sci. 153:1–7. doi:10.1016/j.anireprosci.2014.12.001.
   PubMed Web of Science ®Google Scholar
• Kefer JC, Agarwal A, Sabanegh E. 2009. Role of antioxidants in the treatment of male infertility. Int J Urol. 16:449–457. doi:10.1111/j.1442-2042.2009.02280.x.
   PubMed Web of Science ®Google Scholar
• Kiernan M, Fahey AG, Fair S. 2013. The effect of the in vitro supple-mentation of exogenous long-chain fatty aeids on bovine sperm cellfunction. Reprod Fertil Dev. 25(6):947–954. doi:10.1071/RD12204.
   PubMed Web of Science ®Google Scholar
• Korkmaz F, Malama E, Siuda M, Leiding C, Bollwein H. 2017. Effects of sodium pyruvate on viability, synthesis of reactive oxygen species, lipid peroxidation and DNA integrity of cryopreserved bovine sperm. Anim Reprod Sci. 185:18–27. doi:10.1016/j.anireprosci.2017.07.017.
   PubMed Web of Science ®Google Scholar
• Kumar D, Kumar P, Singh P, Yadav SP, Yadav PS. 2016. Assessment of sperm damages during different stages of cryopreservation in water buffalo by fluorescent probes. Cytotechnology. 68:451–458. doi:10.1007/s10616-014-9798-9.
   PubMed Web of Science ®Google Scholar
• Kumar M, Kumar K, Jain S, Hassan T, Dada R. 2013. Novel insights into the genetic and epigenetic paternal contribution to the human embryo. Clinics. 68:5–14. doi:10.6061/clinics/2013(Sup01)02.
   PubMed Web of Science ®Google Scholar
• Lanz RN, Pickett BW, Komarek RJ. 1965. Effect of lipid additives on pre and post-freeze survival of bovine spermatozoa. J Dairy Sei. 48:1692–1697. doi:10.3168/jds.S0022-0302(65)88553-8.
   Web of Science ®Google Scholar
• Layek SS, Mohanty TK, Kumaresan A, Parks JE. 2016. Cryopreservation of bull semen: evolution from egg yolk based to soybean based extenders. Anim Reprod Sci. 172:1–9. doi:10.1016/j.anireprosci.2016.04.013.
   PubMed Web of Science ®Google Scholar
• Lemma A. 2011. Effect of cryopreservation on sperm quality and fertility. Artif Insemin Farm Anim. 1:191–216.
   Google Scholar
• Lessard C, Parent S, Ledere P, Bailey JL, Sullivan R. 2000. Cryopres-ervation alters the levels of the bull sperm surface protein P25b. J Androl. 21:700–707.
   PubMedGoogle Scholar
• Li P, Li ZH, Dzyuba B, Hulak M, Rodina M, Linhart O. 2010. Evaluating the impacts of osmotic and oxidative stress on common carp (Cyprinus carpio, L.) sperm caused by cryopreservation techniques. Biol Reprod. 83:852–858. doi:10.1095/biolreprod.110.085852.
   PubMed Web of Science ®Google Scholar
• Lv C, Wu G, Hong Q, Quan G. 2018. Spermatozoa cryopreservation: state of art and future in small ruminants. Biopreserv Biobank. 17:171–182. doi:10.1089/bio.2018.0113.
   PubMed Web of Science ®Google Scholar
• Martin ICA. 1963. Effects of lecithin, egg yolk, fructose and period of storage at 5°C on bull spermatozoa frozen to −79°C. J Reprod Fertil. 6:441–449. doi:10.1530/jrf.0.0060441.
   PubMedGoogle Scholar
• Martin-Hidalgo D, Bragado MJ, Batista AR, Oliveira PF, Alves MG. 2019. Antioxidants and male fertility: from molecular studies to clinical evidence. Antioxidants. 8:89. doi:10.3390/antiox8040089.
   Web of Science ®Google Scholar
• Mata-Campuzano M, Álvarez-Rodríguez M, Álvarez M, Tamayo-Canul J, Anel L, De Paz P, Martínez-Pastor F. 2015. Post-thawing quality and incubation resilience of cryopreserved ram spermatozoa are affected by antioxidant supplementation and choice of extender. Theriogenology. 83:520–528. doi:10.1016/j.theriogenology.2014.10.018.
   PubMed Web of Science ®Google Scholar
• Mayer DT, Lesley F. 1945. The factor in egg yolk affecting the resistance, storage potentialities and fertilization capacity of mammalian spermatozoa. J Anim Sci. 4:261–269. doi:10.2527/jas1945.43261x.
   Web of Science ®Google Scholar
• Mazur P. 1963. Kinetics of water loss from cells at subzero temperatures and the likelihood of intracellular freezing. J Gen Physiol. 47:347–369. doi:10.1085/jgp.47.2.347.
   PubMed Web of Science ®Google Scholar
• Mazur P. 1965. Causes of injury in frozen thawed cells. Fed Proc. 24:175–182.
   Google Scholar
• McClean R, MacCallum C, Blyde D, Holt V, Johnston D. 2006. Ultrastructure, osmotic tolerance, glycerol toxicity and cryopreservation of caput and cauda epididymidal kangaroo spermatozoa. Reprod Fertil Dev. 18:469–476. doi:10.1071/RD05148.
   PubMed Web of Science ®Google Scholar
• Medeiros CMO, Forell F, Oliveria ATD, Rodrigues JL. 2002. Currentstatus of sperm cryopreservation: why isn’t it better? Theriogenology. 57(1):327–344. doi:10.1016/S0093-691X(01)00674-4.
   PubMed Web of Science ®Google Scholar
• Mehdipour M, Daghigh Kiaa H, Najafia A, Vaseghi Dodarana H, García-Álvarez O. 2016. Effect of green tea (Camellia sinensis) extract and pre-freezing equilibration time on the post-thawing quality of ram semen cryopreserved in a soybean lecithin-based extender. Cryobiology. 73(3):297–303. doi:10.1016/j.cryobiol.2016.10.008.
   PubMed Web of Science ®Google Scholar
• Melrose DR. 1962. Artificial insemination in cattle. The semen of animals and artificial insemination. England: Commonwealth Agricultural Bureau, Farnham Royal, Bucks; p. 1–181.
   Google Scholar
• Mickle D, Weisel R. 1992. Future directions of vitamin E and its analogues in minimizing myocardial ischemia-reperfusion injury. Can J Cardiol. 9:89–93.
   Web of Science ®Google Scholar
• Mizera A, Kuczaj M, Szul A. 2019. Impact of the Spirulina maxima extract addition to semen extender on bovine sperm quality. Ital J Anim Sci. 18(1):601–607. doi:10.1080/1828051X.2018.1548914.
   Web of Science ®Google Scholar
• Nagasaka R, Okamoto N, Ushio H. 2004. Partial oxidativestress perturbs membrane permeability and fluidity of fish nucleated red blood cells. Comp Biochem Physiol C Toxicol Pharmacol. 139:259–266. doi:10.1016/j.cca.2004.12.001.
   PubMed Web of Science ®Google Scholar
• Navratil AM, Bliss SP, Berghorn KA, Haughian JM, Farmerie TA, Graham JK, Clay CM, Roberson MS. 2003. Constitutive localization on the gonadotropin-releasing hormone (GnRH) receptor to low density membrane microdomains is necessary for GnRH signaling to ERK. J Biol Chem. 278:31593–31602. doi:10.1074/jbc.M304273200.
   PubMed Web of Science ®Google Scholar
• Niki E. 1987. Interaction of ascorbate and alpha-tocopherol. Ann N Y Acad Sci. 498:186–199. doi:10.1111/j.1749-6632.1987.tb23761.x.
   PubMed Web of Science ®Google Scholar
• Norman C, Johnson CE, Porterfield ID, Dunbar RS. 1958. Effect of pH on the lifespan and metabolism of bovine sperm kept at room temperatures. J Dairy Sci. 41:1803–1812. doi:10.3168/jds.S0022-0302(58)91167-6.
   Web of Science ®Google Scholar
• Ortiz A. 2011. High endogenous melatonin concentrations enhance sperm quality and short-term in vitro exposure to melatonin improves aspects of sperm motility. J Pineal Res. 50:132–139. doi:10.1111/j.1600-079X.2010.00822.x.
   PubMed Web of Science ®Google Scholar
• Parks JE, Lynch DV. 1992. Lipid composition and thermotropic phasebehavior of boar, bull, stallion and rooster sperm membrane. Cryobiology. 29:255–266. doi:10.1016/0011-2240(92)90024-V.
   PubMed Web of Science ®Google Scholar
• Pérez-Crespo M, Moreira P, Pintado B, Gutiérrez-Adán A. 2008. Factors from damaged sperm affect its DNA integrity and its ability to promote embryo implantation in mice. J Androl. 29(1):47–54. doi:10.2164/jandrol.107.003194.
   PubMedGoogle Scholar
• Peris SI, Bilodeau J-F, Dufour M, Bailey JL. 2007. Impact of cryopreservation and reactive oxygen species on DNA integrity, lipid peroxidation, and functional parameters in ram sperm. Mol Reprod Dev. 74:878–892. doi:10.1002/mrd.20686.
   PubMed Web of Science ®Google Scholar
• Phillips PH. 1939. Preservation of bull semen. J Biol Chem. 130:415.
   Google Scholar
• Phillips PH, Lardy HA. 1940. A yolk-buffer pabulum for the preservation of bull semen. J Dairy Sci. 23:399–404. doi:10.3168/jds.S0022-0302(40)95541-2.
   Google Scholar
• Pickett BW, Berndtson WE. 1974. Preservation of bovine spermatozoa by freezing in straws: a review. J Dairy Sci. 57:1287–1301. doi:10.3168/jds.S0022-0302(74)85058-7.
   PubMed Web of Science ®Google Scholar
• Pickett BW, Berndtson WE. 1978. Principles and techniques of freezing spermatozoa. Physiology of reproduction and artificial insemination of cattle. San Francisco: Freeman; p. 494–554.
   Google Scholar
• Pini T, Leahy T, de Graaf SP. 2018. Sublethal sperm freezing damage: manifestations and solutions. Theriogenology. 118:172–181. doi:10.1016/j.theriogenology.2018.06.006.
   PubMed Web of Science ®Google Scholar
• Polge C, Rowson LEA. 1952. Results with bull semen stored at y79°C. Vet Rec. 64:851–853.
   Google Scholar
• Purdy PH. 2006. A review on goat sperm cryopreservation. Small Rumin Res. 63:215–225. doi:10.1016/j.smallrumres.2005.02.015.
   Web of Science ®Google Scholar
• Ramírez-Vasquez RRA, Cano A, Hozbor FA, Cesari A. 2019. Cryopreservation and egg yolk extender components modify the interaction between seminal plasma proteins and the sperm surface. Theriogenology. 140:153‐163. doi:10.1016/j.theriogenology.2019.08.025.
   PubMed Web of Science ®Google Scholar
• Reddy NSS, Mohanarao GJ, Atreja SK. 2010. Effects of adding taurine and trehalose to a tris-based egg yolk extender on buffalo(Bubalua bubalis) sperm quality following cryopreservation. Anim Reprod Sci. 119:183–190. doi:10.1016/j.anireprosci.2010.01.012.
   PubMed Web of Science ®Google Scholar
• Rodriguez OL, Berndtson WE, Ennen BD, Pickett W. 1975. Effect of rates of freezing, thawing and level of glycerol on the survival of bovine spermatozoa in straws. J Anim Sci. 41:129–136. doi:10.2527/jas1975.411129x.
   PubMed Web of Science ®Google Scholar
• Royere D, Barthelemy C, Hamamah S, Lansac J. 1996. Cryopreservationof spermatozoa: 1996 a review. Hum Reprod Update. 2(6):553–559. doi:10.1093/humupd/2.6.553.
   PubMed Web of Science ®Google Scholar
• Samper JC, Hellander JC, Crabo BG. 1991. Relationship between the fertility of fresh and frozen stallion semen and semen quality. J Reprod Fertil Suppl. 44:107–114.
   PubMedGoogle Scholar
• Sarıözkan S, Numan Bucak M, Pürhan T, Büyükleblebicie S, Ekenf A, Akayg C. 2015. Influence of fetuin and hyaluronan on the post-thaw quality and fertilizing ability of Holstein bull semen. Cryobiology. 71(1):119–124. doi:10.1016/j.cryobiol.2015.04.011.
   PubMed Web of Science ®Google Scholar
• Shah SAH, Andrabi SMH, Qureshi IZ. 2017. Freezability of water buffalo bull (Bubalus bubalis) spermatozoa is improved with the addition of curcumin (diferuoyl methane) in semen extender. Andrologia. 49(8):127–131. doi:10.1111/and.12713.
   Web of Science ®Google Scholar
• Shannon P. 1965. Contribution of seminal plasma, sperm numbers and gas phase to dilution effects of bovine spermatozoa. J Dairy Sci. 48:1357–1361. doi:10.3168/jds.S0022-0302(65)88463-6.
   PubMed Web of Science ®Google Scholar
• Sharma RK, Agarwal A. 1996. Role of reactive oxygen species in male infertility. Urology. 48:835–850. doi:10.1016/S0090-4295(96)00313-5.
   PubMed Web of Science ®Google Scholar
• Shiva M, Gautam AK, Verma Y, Shivgotra V, Doshi H, Kumar S. 2011. Association between sperm quality, oxidative stress, and seminal antioxidant activity. Clin Biochem. 44:319–324. doi:10.1016/j.clinbiochem.2010.11.009.
   PubMed Web of Science ®Google Scholar
• Sierens J, Hartley J, Campbell M, Leathem A, Woodside J. 2002. In vitro isoflavone supplementation reduces hydrogen peroxide-induced DNA damage in sperm. Teratog Carcinog Mutagen. 22:227–234. doi:10.1002/tcm.10015.
   PubMedGoogle Scholar
• Singh M, Sharma A. 2018. Improvement in quality of frozen Jersey bull semen following fortification with chloroquine diphosphate and ascorbic acid. Indian J Anim Sci. 88(7):791–794.
   Web of Science ®Google Scholar
• Soren S, Singh SV, Kumar S. 2017. Effect of astaxanthin supplementation on semen (Karan Fries Bulls) storage at 5 C. Int J Curr Microbiol Appl Sci. 6(5):23–28. doi:10.20546/ijcmas.2017.605.003.
   Google Scholar
• Tarig AA, Wahid H, Rosnina Y, Yimer N, Goh YM, Baiee FH, Khumran AM, Salman H, Assi MA, Ebrahimi M. 2017. Effect of different concentrations of soybean lecithin and virgin coconut oil in Tris-based extender on the quality of chilled and frozen-thawed bull semen. Vet World. 10(6):672–678. doi:10.14202/vetworld.2017.672-678.
   PubMed Web of Science ®Google Scholar
• Tavalaee M, Razavi S, Nasr-Esfahani MH. 2009. Influence of sperm chromatin anomalies on assisted reproductive technology outcome. Fertil Steril. 91(4):1119–1126. doi:10.1016/j.fertnstert.2008.01.063.
   PubMed Web of Science ®Google Scholar
• Taylor K, Roberts P, Sanders K, Burton P. 2009. Effect of antioxidant supplementation of cryopreservation medium on post-thaw integrity of human spermatozoa. Reprod Biomed Online. 18:184–189. doi:10.1016/S1472-6483(10)60254-4.
   PubMed Web of Science ®Google Scholar
• Thomson L, Fleming S, Aitken R, De Iuliis G, Zieschang JA, Clark A. 2009. Cryopreservation-induced human sperm DNA damage is predominantly mediated by oxidative stress rather than apoptosis. Hum Reprod. 24(9):2061–2070.
   Web of Science ®Google Scholar
• Tvrda E, Mackovich A, Greifova H, Hashim F, Lukac N. 2017. Antioxidant effects of lycopene on bovine sperm survival and oxidative profile following cryopreservation. Vet Med (Praha). 62(8):429–436. doi:10.17221/86/2017-VETMED.
   Web of Science ®Google Scholar
• Ugur MR, Abdelrahman AS, Evans HC, Gilmore AA, Hitit M, Arifiantini RI, Purwantara B, Kaya A, Memili E. 2019. Advances in cryopreservation of bull sperm. Front Vet Sci. 6:268. doi:10.3389/fvets.2019.00268.
   PubMed Web of Science ®Google Scholar
• Uysal O, Bucak MN. 2007b. Effects of oxidized glutathione, bovine serum albumin, cysteine and lycopene on the quality of frozen-thawed ram semen. Acta Vet Brno. 76(3):383–390. doi:10.2754/avb200776030383.
   Web of Science ®Google Scholar
• Vahedi V, Hedayat Evrigh N, Behroozlak M, Dirandeh E. 2018. Antioxidant effects of thyme (Thymus vulgaris) extract on ram sperm quality during cryopreservation. Iran J Appl Anim Sci. 8(2):263–269.
   Web of Science ®Google Scholar
• Vale WG, Silva AOA, Sousa JS, Ribeiro HFL, de Souza Hem, Nahum BS 1997. Preliminary report on the use of coconut water (Cocos nucifera) as a diluter of buffalo semen. In Embrapa Amazônia Oriental-Artigo em anais de congresso (ALICE). In World Buffalo Congress, 5. Caserta (Italy). p. 836–839.
   Google Scholar
• Van Demark NL, Miller WJ, Kinney WC Jr, Rodriguez C, Friedman ME. 1957. The preservation of bull semen at sub-zero temperatures. Bulletin (University of Illinois [Urbana Champaign Campus], Agricultural Experiment Station), 621.
   Google Scholar
• Van Demark NL, Sharma UD. 1957. Preliminary fertility results from the preservation of bovine semen at room temperatures. J Dairy Sci. 40:438–439. doi:10.3168/jds.S0022-0302(57)94501-0.
   Web of Science ®Google Scholar
• Vera-Munoza O, Amirat-Brianda L, Diaz T, Vásquez L, Schmidt E, Desherces S, Anton M, Bencharif D, Tainturiera D. 2009. Effect of semen dilution to low-sperm number per dose on motility and functionality of cryopreserved bovine spermatozoa using low-density lipoproteins (LDL) extender: comparison to Triladyl® and Bioxcell®. Theriogenology. 71(6):895–900. doi:10.1016/j.theriogenology.2008.10.010.
   PubMed Web of Science ®Google Scholar
• Verma A, Rajput S, De S, Kumar R, Chakravarty AK, Datta TK. 2014. Genome-wide pro fi ling of sperm DNA methylation in relation to buffalo (Bubalus bubalis) bull fertility. Theriogenology. 82:750–759. doi:10.1016/j.theriogenology.2014.06.012.
   PubMed Web of Science ®Google Scholar
• Wang AW, Zhang H, Ikemoto I, Anderson DJ, Loughlin KR. 1997. Reactive oxygen species generation by seminal cells during cryopreservation. Urology. 49:921–925. doi:10.1016/S0090-4295(97)00070-8.
   PubMed Web of Science ®Google Scholar
• Watson PF. 1979. The preservation of semen in mammals. Oxford Rev Reprod Biol. 1:283–350.
   Google Scholar
• Watson PF. 1995. Recent developments and concepts in the cryopreservation of spermatozoa and the assessment of their post thawing function. Reprod Fertil Dev. 7:871–891. doi:10.1071/RD9950871.
   PubMed Web of Science ®Google Scholar
• Watson PF. 2000. The causes of reduced fertility with cryopreservedsemen. Anim Reprod Sci. 60–61:481–492. doi:10.1016/S0378-4320(00)00099-3.
   PubMed Web of Science ®Google Scholar
• White IG 1956. The effect of some inorganic ions on mammalian spermatozoa. Proc. 3rd Int. Congr. Anim. Reprod. A.I. Cambridge, U.K., Vol. 1, 23–25.
   Google Scholar
• Willett EL, Salisbury GW. 1942. The effect of various dilutors, cooling rate, temperature of storage, and some other factors on the livability of spermatozoa in stored samples of bull semen. Mem Cornell Univ Agric Exp Stn. 249:45.
   Google Scholar
• Wongtawan T, Saravia F, Wallgren M, Caballero I, Rodriguez-Martinez H. 2006. Fertility after deep intra-uterine artificial inseminationof concentrated low-volume boar semen doses. Theriogenology. 65:773–787. doi:10.1016/j.theriogenology.2005.07.003.
   PubMed Web of Science ®Google Scholar
• Yang SM, Wang T, Wen DG, Hou JQ, Li HB. 2016. Protective effect of Rhodiola rosea polysaccharides on cryopreserved boar sperm. Carbohydr Polym. 1(135):44–47. doi:10.1016/j.carbpol.2015.08.081.
   Google Scholar
• Yoon SJ, Kwon WS, Rahman MS, Lee JS, Pang MG. 2015. A novel approach to identifying physical markers of cryo-damage in bull spermatozoa. PLoS ONE. 10:e0126232. doi:10.1371/journal.pone.0126232.
   Web of Science ®Google Scholar
• Yoshida M. 2000. Conservation of sperms: current status and new trends.Anim. Reprod Sci. 60–61:349–355. doi:10.1016/S0378-4320(00)00125-1.
   Google Scholar
• Zhang J, Robinson D, Salmon P. 2006. A novel function for selenium in biological system: selenite as a highly effective iron carrier for Chinese hamster ovary cell growth and monoclonal antibody production. Biotechnol Bioeng. 95:1188–1197. doi:10.1002/bit.21081.
   PubMed Web of Science ®Google Scholar
• Zini A, Boman JM, Belzile E, Ciampi A. 2008. Sperm DNA damage is associated with an increased risk of pregnancy loss after IVF and ICSI: systematic review and meta-analysis. Hum Reprod. 23(12):2663–2668. doi:10.1093/humrep/den321.
   PubMed Web of Science ®Google Scholar