Antioxidant effects of bovine serum albumin on kinetics, microscopic and oxidative characters of cryopreserved bull spermatozoa
Abstract
The aim of this study was to determine the effects of bovine serum albumin (BSA) as an antioxidant on post-thaw characters of bull spermatozoa such as motion variables, viability, plasma membrane integrity, morphology, lipid peroxidation, total antioxidant capacity (TAC), total thiols (TT) and the enzymes activities. Ejaculates were collected from six proven bulls and diluted with a citrate-based extender supplemented with various concentrations of BSA (0, 0.5, 1, 1.5 and 2 g/100 mL). The results showed that the semen extender supplemented with various concentrations of BSA increased (p0.05) were detected in progressive motility, sperm track straightness, beat cross frequency, curvilinear velocity and malondialdehyde production between the experimental groups. The highest concentration of BSA (2 g/100 mL) in the semen extender reduced (p<0.05) the sperm motion variables. The results indicated that the most effective concentration of BSA is 1 g/100 mL in the semen extender which is associated with an increase in the total motility, antioxidant enzymes activities, TT and TAC.Downloads
References
Aitken RJ, 1995. Free radicals, lipid peroxidation and sperm function. Reprod Fertil Dev 7: 659-668. http://dx.doi.org/10.1071/RD9950659 PMid:8711202
Aitken RJ, Clarkson JS, 1987. Cellular basis of defective sperm function and its association with the genesis of reactive oxygen species by human spermatozoa. J Reprod Fertil 81: 459-469. http://dx.doi.org/10.1530/jrf.0.0810459 PMid:2828610
Alvarez JG, Storey BT, 1982. Spontaneous lipid peroxidation in rabbit epididymal spermatozoa: its effect on sperm motility. Biol Reprod 27: 1102-1108. http://dx.doi.org/10.1095/biolreprod27.5.1102 PMid:6297627
Alvarez JG, Storey BT, 1983. Taurine, hypotaurine, epinephrine and albumin inhibit lipid peroxidation in rabbit spermatozoa and protect against loss of motility. Biol Reprod 29: 548-555. http://dx.doi.org/10.1095/biolreprod29.3.548 PMid:6626644
Alvarez JG, Storey BT, 1984. Assessment of cell damage caused by spontaneous lipid peroxidation in rabbit spermatozoa. Biol Reprod 30: 323-331. http://dx.doi.org/10.1095/biolreprod30.2.323 PMid:6231058
Alvarez JG, Storey BT, 1989. Role of glutathione peroxidase in protecting mammalian spermatozoa from loss of motility caused by spontaneous lipid peroxidation. Gamete Res 23: 77-90. http://dx.doi.org/10.1002/mrd.1120230108 PMid:2545584
Balestri F, Giannecchini M, Sgarrella F, Carta MC, Tozzi MG, Camici M, 2007. Purine and pyrimidine nucleosides preserve human astrocytoma cell adenylate energy charge under ischemic conditions. Neurochem Int 50: 517-523. http://dx.doi.org/10.1016/j.neuint.2006.10.005 PMid:17126452
Bamba K, Cran DG, 1992. Effects of treatment with butylated hydroxytoluene on the susceptibility of boar spermatozoa to cold stress and dilution. J Reprod Fertil 95: 69-77. http://dx.doi.org/10.1530/jrf.0.0950069 PMid:1625251
Baumber J, Ball BA, Gravance CG, Medina V, Davies-Morel MC, 2000. The effect of reactive oxygen species on equine sperm motility, viability, acrosomal integrity, mitochondrial membrane potential, and membrane lipid peroxidation. J Androl 21: 895-902. PMid:11105916
Bennet PJ, Moatti JP, Mansat A, Ribbes H, Cayrac JC, Pontonnier F, Chap H, Douste-Blazy L, 1987. Evidence for the activation of phospholipases during acrosome reaction of human sperm elicited by calcium ionophore A23187. Biochim Biophys Acta 919: 255-265. http://dx.doi.org/10.1016/0005-2760(87)90265-7
Benzie IF, Strain JJ, 1996. The ferric reducing ability of plasma (FRAP) as a measure of "antioxidant power": the FRAP assay. Anal Biochem 239: 70-76. http://dx.doi.org/10.1006/abio.1996.0292 PMid:8660627
Bilodeau JF, Blanchette S, Cormier N, Sirard MA, 2001. Thiols prevent H2O2-mediated loss of sperm motility in cryopreserved bull semen. Theriogenology 56: 275-286. http://dx.doi.org/10.1016/S0093-691X(01)00562-3
Bilodeau JF, Blanchette S, Cormier N, Sirard MA, 2002. Reactive oxygen species-mediated loss of bovine sperm motility in egg yolk Tris extender: protection by pyruvate, metal chelators and bovine liver or oviductal fluid catalase. Theriogenology 57: 1105-1122. http://dx.doi.org/10.1016/S0093-691X(01)00702-6
Buckett WM, Luckas MJ, Aird IA, Farquharson RG, Kingsland CR, Lewis-Jones DI, 1997. The hypo-osmotic swelling test in recurrent miscarriage. Fertil Steril 68, 506-509. http://dx.doi.org/10.1016/S0015-0282(97)00241-0
Buege JA, Aust SD, 1978. Microsomal lipid peroxidation methods. Enzymol 52: 302 - 310.
de Lamirande E, Gagnon C, 1993. Human sperm hyperactivation and capacitation as parts of an oxidative process. Free Radic Biol Med 14: 157-166. http://dx.doi.org/10.1016/0891-5849(93)90006-G
Donoghue AM, Donoghue DJ, 1997. Effects of water- and lipid-soluble antioxidants on turkey sperm viability, membrane integrity, and motility during liquid storage. Poult Sci 76: 1440-1445. PMid:9316122
Fialkow L, Chan C.K, Rotin D, Grinstein S, Downey GP, 1994. Activation of the mitogen-activated protein kinase signaling pathway in neutrophils. Role of oxidants. J Biol Chem 269:31234-31242. PMid:7983067
Gil J, Lundeheim N, Soderquist L, Rodriguez-Martinez H, 2003. Influence of extender, temperature, and addition of glycerol on post-thaw sperm parameters in ram semen. Theriogenology 59: 1241-1255. http://dx.doi.org/10.1016/S0093-691X(02)01177-9
Gil-Guzman E, Ollero M, Lopez MC, Sharma RK, Alvarez JG, Thomas AJ Jr, Agrawal A, 2001. Differential production of reactive oxygen species by subsets of human spermatozoa at different stages of maturation. Hum Reprod 16: 1922-1930. http://dx.doi.org/10.1093/humrep/16.9.1922 PMid:11527899
Gillan L, Maxwell WM, 1999. The functional integrity and fate of cryopreserved ram spermatozoa in the female tract. J Reprod Fertil Suppl 54: 271-283. PMid:10692861
Irvine DS, 1996. Glutathione as a treatment for male infertility. Rev Reprod 1, 6-12. http://dx.doi.org/10.1530/ror.0.0010006 PMid:9414432
Jeulin C, Soufir JC, Weber P, Laval-Martin D, Calvayrac R, 1989. Catalase activity in human spermatozoa and seminal plasma. Gamete Res 24: 185-196. http://dx.doi.org/10.1002/mrd.1120240206 PMid:2793057
Klem ME, Jr Kreider JL, Pruitt JB, Potter GD, 1986. Motility and fertility of equine spermatozoa extended in bovine serum albumin and sucrose. Theriogenology 26: 569-576. http://dx.doi.org/10.1016/0093-691X(86)90163-9
Kreider JL, Tindall WC, Potter GD, 1985. Inclusion of bovine serum albumin in semen extenders to enhance maintenance of stallion sperm viability. Theriogenology 23: 399-408. http://dx.doi.org/10.1016/0093-691X(85)90042-1
Lewis SE, Sterling ES, Young IS, Thompson W, 1997. Comparison of individual antioxidants of sperm and seminal plasma in fertile and infertile men. Fertil Steril 67: 142-147. http://dx.doi.org/10.1016/S0015-0282(97)81871-7
Lornage J, Guerin JF, Czyba JC, Menezo Y, 1983. Influence of cations and albumin on human spermatozoa. Arch Androl 10: 119-125. http://dx.doi.org/10.3109/01485018308987552 PMid:6860035
Macleod J, 1951. Sulfhydryl groups in relation to the metabolism and motility of human spermatozoa. J Gen Physiol 34: 705-714. http://dx.doi.org/10.1085/jgp.34.5.705 PMid:14832448 PMCid:PMC2147277
Marklund S, Marklund G, 1974. Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur J Biochem 47: 469-474. http://dx.doi.org/10.1111/j.1432-1033.1974.tb03714.x PMid:4215654
Meyers SA, 2005. Spermatozoal response to osmotic stress.Anim Reprod Sci 89: 57-64. http://dx.doi.org/10.1016/j.anireprosci.2005.06.026 PMid:16084042
Nair SJ, Brar AS, Ahuja CS, Sangha SP, Chaudhary KC, 2006. A comparative study on lipid peroxidation, activities of antioxidant enzymes and viability of cattle and buffalo bull spermatozoa during storage at refrigeration temperature. Anim Reprod Sci 96: 21-29. http://dx.doi.org/10.1016/j.anireprosci.2005.11.002 PMid:16337101
Pena FJ, Rodriguez Martinez H, Tapia JA, Ortega Ferrusola C, Gonzalez Fernandez L, Macias Garcia B, 2009. Mitochondria in mammalian sperm physiology and pathology: a review. Reprod Domest Anim 44: 345-349. http://dx.doi.org/10.1111/j.1439-0531.2008.01211.x PMid:19144010
Peris SI, Bilodeau JF, 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. http://dx.doi.org/10.1002/mrd.20686 PMid:17186553
Roca J, Rodriguez MJ, Gil MA, Carvajal G, Garcia EM, Cuello C, Vazquez JM, Martinez EA, 2005. Survival and in vitro fertility of boar spermatozoa frozen in the presence of superoxide dismutase and/or catalase. J Androl 26: 15-24. PMid:15611562
Schafer S, Holzmann A, 2000. The use of transmigration and spermac stain to evaluate epididymal cat spermatozoa. Anim Reprod Sci 59: 201-211. http://dx.doi.org/10.1016/S0378-4320(00)00073-7
SedlakJ, Lindsay R.H, 1968. Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman's reagent. Anal Biochem 25: 192-205. http://dx.doi.org/10.1016/0003-2697(68)90092-4
Sikka SC, 1996. Oxidative stress and role of antioxidants in normal and abnormal sperm function. Front Biosci 1: e78-86. PMid:9159248
Uto N, Yamahama Y, 1996. The motility and fertility of golden hamster sperm cultured in BSA-free medium. Biol Cell 88: 23-28. http://dx.doi.org/10.1016/S0248-4900(97)86827-X
Wales RG, White IG, Lamond DR, 1959. The spermicidal activity of hydrogen peroxide in vitro and in vivo. J Endocrinol 18: 236-244. http://dx.doi.org/10.1677/joe.0.0180236 PMid:13664846
Watson PF, 2000. The causes of reduced fertility with cryopreserved semen. Anim Reprod Sci 60-61: 481-492. http://dx.doi.org/10.1016/S0378-4320(00)00099-3
White IG, 1955. The toxicity of heavy metals to mammalian spermatozoa. Aust J Exp Biol Med Sci 33: 359-366. http://dx.doi.org/10.1038/icb.1955.36 PMid:13260077
© CSIC. Manuscripts published in both the print and online versions of this journal are the property of the Consejo Superior de Investigaciones Científicas, and quoting this source is a requirement for any partial or full reproduction.
All contents of this electronic edition, except where otherwise noted, are distributed under a Creative Commons Attribution 4.0 International (CC BY 4.0) licence. You may read the basic information and the legal text of the licence. The indication of the CC BY 4.0 licence must be expressly stated in this way when necessary.
Self-archiving in repositories, personal webpages or similar, of any version other than the final version of the work produced by the publisher, is not allowed.