Have a personal or library account? Click to login
The Effects of Antioxidants Provided with Feed on Certain Quality Parameters of Bull Semen Under Heat Stress Conditions Cover

The Effects of Antioxidants Provided with Feed on Certain Quality Parameters of Bull Semen Under Heat Stress Conditions

Open Access
|Dec 2020

References

  1. 1. Bucak MN, Sariözkan S, Tuncer PB, Sakin F, Ateṣṣahin A, Kulaksiz R, Çevik M: The effect of antioxidants on post-thawed Angora goat (Capra hircusancryrensis) sperm parameters, lipid peroxidation and antioxidant activities. Small Rumin Res. 2010, 89:1:24–30.10.1016/j.smallrumres.2009.11.015
  2. 2. Büyükleblebici O, Büyükleblebici S, Taşdemir U, Tuncer PB:The Effects of DifferentAntioxidants on Post-thaw Microscopic and Oxidative Stress Parameters in the Cryopreservation of Brown-Swiss Bull Semen. Kafkas Universitesi Veteriner Fakultesi Dergisi 2016, 22 (1):101-107.
  3. 3. Sikka SC, Rajasekaran M, Hellstrom WJG: Role of oxidative stress and antioxidants in male infertility. J Androl. 1995, 16:6:464–468.10.1002/j.1939-4640.1995.tb00566.x
  4. 4. Brito LFC, Silva A, Rodrigues EDF, Vieira LH, Vderagon F, Kastelic LAG: Effect ofenvironmental factors, age and genotype on sperm production and semen quality in Bos indicus and Bos taurus AI bulls, Brazil. Anim Reprod Sci. 2002, 70:181–190.10.1016/S0378-4320(02)00009-X
  5. 5. Majic-Balic I, Milinkovic-Tur S, Samardzija M, Vince S: Effect of age and environmental factors on semen quality, glutathione peroxidase activity and oxidative parameters in Simmental bulls. Theriogenology 2012, 78:423–431.10.1016/j.theriogenology.2012.02.022
  6. 6. Morrell JM: Heat stess and bull fertility. Theriogenology 2020, 153:62-67.10.1016/j.theriogenology.2020.05.014
  7. 7. Rahal A, Kumar A, Singh V, Yadav B, Tiwari R, Chakraborty S, Dhama K: Oxidative stress, prooxidants, and antioxidants: the interplay. BioMed Res Int. 2014, 19: http://dx.doi.org/10.1155/2014/761264.10.1155/2014/761264
  8. 8. O’Flaherty CM: The enzymatic antioxidant system of human spermatozoa. Adv Androl. 2014, 626374:15.10.1155/2014/626374
  9. 9. Desai NR, Mahfouz R, Sharma R, Gupta S, Agarwal A: Reactive oxygen species levels are independent of sperm concentration, motility, and abstinence in a normal, healthy, proven fertile man: a longitudinal study. Fertil Steril. 2010, 94:4:1541–1543.10.1016/j.fertnstert.2009.12.041
  10. 10. Agarwal A, Makker K, Sharma R: Clinical relevance of oxidative stress in male factor infertility: an update. Am J Reprod Immunol. 2008, 59:1:2–1110.1111/j.1600-0897.2007.00559.x
  11. 11. Jones R, Mann T: Lipid peroxidation in spermatozoa. Proceedings of the Royal Society of London-Biological Science 1973, 184:103–107.10.1098/rspb.1973.0035
  12. 12. Beconi MT, Affranchino MA, Schang LM, Beorlegui NB: Influence of antioxidants on SOD activity in bovine sperm. Biochem Int. 1991, 23:545–553.
  13. 13. Beconi MT, Francia CR, Mora NG, Affranchino MA: Effect of natural antioxidants on frozen bovine semen preservation. Theriogenology 1993, 40:841–851.10.1016/0093-691X(93)90219-U
  14. 14. Brouwers JF, Gadella BM: In situ detection and localization of lipid peroxidation in individual bovine sperm cells. Free Radic Biol Med. 2003, 35:1382–1391.10.1016/j.freeradbiomed.2003.08.010
  15. 15. Bansal AK, Bilaspuri GS: Impacts of oxidative stress and antioxidants on semen functions. Vet Med Int. 2011, 2011:1-7.10.4061/2011/686137
  16. 16. Nichi M, Bols PE, Züge RM, Barnabe VH, Goovaerts IG, Barnabe RC, Cortada CN: Seasonal variation in semen quality in Bosindicus and Bos taurusbulls raised under tropical conditions. Theriogenology 2006, 66:822–828.10.1016/j.theriogenology.2006.01.056
  17. 17. Rahman MB, Vandaele L, Rijsselaere T, Maes D, Hoogewijs M, Frijters A et al.: Scrotal insulation and its relationship to abnormal morphology, chromatin protamination and nuclear shape of spermatozoa in Holstein-Friesian and Belgian Blue bulls. Theriogenology 2011, 76:1246-1257.10.1016/j.theriogenology.2011.05.031
  18. 18. Kim JG, Parthasarathy S: Oxidation and the spermatozoa. Semin Reprod Endocrinol. 1998, 16:4:235–239.10.1055/s-2007-1016283
  19. 19. Miller JK, Brzezinska-Slebodzinska E, Madsen FC: Oxidative stress, antioxidants, and animal function. J Dairy Sci. 1993, 76:9:2812–2823.10.3168/jds.S0022-0302(93)77620-1
  20. 20. Kumar H, Mahmood S: The use of fast acting antioxidants for the reduction of cow placental retention and subsequent endometritis. Indian J Anim Sci. 2001, 71:7:650–653.
  21. 21. Korzeniowska M, Madej J,Stefaniak T, Kopec W: Influence of selenium on the morphology of immune system organs in healthy broilers. Acta Vet-Beograd 2019, 69(4):379-390.10.2478/acve-2019-0032
  22. 22. Milanovic Svetlana, Jovanovic BIvan, Bjelica Jelena, Joksimovic S, Stefanovic S, Magdalena Radovic, Kirovski Danijela, Valcic Olivera, Gvozdic Dragan: The influence of selenium and deiodinases blockers on juvenile rats body weight. Veterinarski Glasnik 2014, 68(1-2):3 9. https://doi.org/10.2298/VETGL1402003M10.2298/VETGL1402003M
  23. 23. Milanovic Svetlana, Jovanovic Ivan, Valcic Olivera: Selenoproteins. Veterinarski Glasnik 2015, 69(1-2):75-89. https://doi.org/10.2298/VETGL1502075M10.2298/VETGL1502075M
  24. 24. Jimenez C, Lefrancois AM, Ghyselinck NB, Dufaure JP: Characterization and hormonal regulation of 24 kDa protein synthesis by the adult murine epididymis. J Endocrinol. 1992, 133:197-203.10.1677/joe.0.13301971613422
  25. 25. Vernet P, Faure J, Dufaure JP, Drevet JR: Tissue and developmental distribution, dependence upon testicular factors and attachment to spermatozoa of GPx5, a murine epididymisspecific glutathione peroxidase. Mol Reprod Dev. 1997, 47:87-98.10.1002/(SICI)1098-2795(199705)47:1<87::AID-MRD12>3.0.CO;2-X
  26. 26. Roeckel-Drevet P, Gagne G, Tourvieille de Labrouhe D, Dufaure JP, Nicolas P, Drevet JR: Molecular characterization, organ distribution and stress-mediated induction of two glutathione peroxidase-encoding mRNAs in sunflower, Helianthus annuus. Physiol Plant. 1998, 103:385-394.10.1034/j.1399-3054.1998.1030312.x
  27. 27. Rejraji H, Vernet P, Drevet JR: GPX5 is present in the mouse caput and cauda epididymidislumen at three different locations. Mol Reprod Dev. 2002, 63:96-103.10.1002/mrd.10136
  28. 28. Rejraji H, Drevet JR: Secretions apocrines dans le tractus genital male, roles potentiels dans la maturation des gametes. Andrologie 2004, 1:22-33.10.1007/BF03035465
  29. 29. Schwaab V, Lareyre JJ, Vernet P, Pons E, Faure J, Dufaure JP, Drevet JR: Characterization, regulation of the expression and putative roles of two glutathione peroxidase proteins found in the mouse epididymis. J Reprod Fertil. 1998, Supplement, 53:157-162.
  30. 30. Gadea J, Sellés E, Marco MA, Coy P, Matás C, Romar R, Ruiz S: Decrease in glutathione content in boar sperm after cryopreservation. Effect of the addition of reduced glutathione to the freezing and thawing extenders. Theriogenology 2004, 62:690–701.10.1016/j.theriogenology.2003.11.013
  31. 31. Imai H, Suzuki K, Ishizaka K, Ichinose S, Oshima H, Okayasu I, Emoto K, Umeda M, Nakagawa Y: Failure of the expression of phospholipid hydroperoxide glutathione peroxidase in the spermatozoa of human infertile males. Biol Reprod. 2001, 64:674–683.10.1095/biolreprod64.2.674
  32. 32. Stradaioli G, Sylla L, Monaci M, Maiorino M: Phospholipid hydroperoxide glutathione peroxidase in bull spermatozoa provides a unique marker in the quest for semen quality analysis. Theriogenology 2009, 72:91–98.10.1016/j.theriogenology.2009.02.006
  33. 33. Misra HP, Fridovich I: The role of superoxide anion in the antioxidation of epinephrine and a simple assay for superoxide dismutase. J Biol Chem. 1972, 247:3170-3175.10.1016/S0021-9258(19)45228-9
  34. 34. Günzler WA, Stefens GJ, Grossmann A, Kim SMA, Ötting F, Wendel A, Flohé L: The amino-acid sequence of bovine glutathione peroxidase. Biol Chem. 1984, 365:195-212.10.1515/bchm2.1984.365.1.195
  35. 35. Trevisan M, Browne R, Ram M, Muti P, Freudenheim J, Carosella AM, Armstrong D: Correlates of markers of oxidative status in the general population. Am J Epidemiol. 2001, 154:348-356.10.1093/aje/154.4.348
  36. 36. Williams CA, Kronfeld DS, Hess TM, Saker KE, Waldron JN, Crandell KM, Hoffman RM, Harris PA: Antioxidant supplementation and subsequent oxidative stress of horses during an 80-km endurance race. J Anim Sci. 2002, 82:588-594.10.2527/2004.822588x
  37. 37. Asadpour R, Tayefi-Nasrabadi H: Seasonal variation in antioxidant enzyme activity in seminal plasma in Holstein bulls. Comp Clin Path. 2012, 21:2:173-176.10.1007/s00580-010-1080-8
  38. 38. Cassani P, Beconi MT, O’Flaherty C: Relationship between total superoxide dismutase activity with lipid peroxidation, dynamics and morphological parameters in canine semen. Anim Reprod Sci. 2005, 86:163-173.10.1016/j.anireprosci.2004.06.006
  39. 39. Partyka A, Łukaszewicz E, Niżański W: Effect of cryopreservation on sperm parameters, lipid peroxidation and antioxidant enzymes activity in fowl semen. Theriogenology 2012,77:8: 1497-1504.10.1016/j.theriogenology.2011.11.006
  40. 40. Bilodeau JF, Chatterjee S, Sirard MA, Gagnon C: Levels of antioxidant defenses are decreased in bovine spermatozoa after a cycle of freezing and thawing. Mol Reprod Dev. 2000, 55:282-288.10.1002/(SICI)1098-2795(200003)55:3<282::AID-MRD6>3.0.CO;2-7
  41. 41. Kadirve G, Kumar S, Ghosh SK, Perumal P: Activity of antioxidative enzymes in fresh and frozen thawed buffalo (Babalus bubalis) spermatozoa in relation to lipid peroxidation and semen quality. Asian Pac J Reprod. 2014, 3(3):210-217.10.1016/S2305-0500(14)60028-2
  42. 42. Vince S, Zura ZI, Samardzija M, Majic BI, Vilic M, Đuricic D, Valpotic H, Markovic F, Milinkovic-Tur S: Age-related differences of semen quality, seminal plasma and spermatozoa antioxidative and oxidative stress variables in bulls during cold and warm periods of the year. Animal 2018, 12:3:559-568.10.1017/S1751731117001811
  43. 43. Soren S, Singh SV, Singh P: Influence of season on seminal antioxidant enzymes in Karan Fries bulls under tropical climatic conditions. Turk J Vet Anim Sci. 2016, 40:797-802.10.3906/vet-1603-76
  44. 44. Nair JS, Brar AS, Ahuja CC, Sangha SPS, Chaudhary KC: A comoparative study on lipid peroxidation, activities of antioxidant enzymes and viability of cattle and buffalo bull spermatozoa during storage at refrigeration temperature. Anim Reprod Sci. 2006, 96:21-29.10.1016/j.anireprosci.2005.11.002
  45. 45. Sariözakan S, Tuncer PB, Bucak MN, Ulutaṣ PA: Influence of various antioxidants on microscopic-oxidative stress indicators and fertilizing ability of frozen-thawed bull semen. Acta Vet Brno 2009, 78:463-469.10.2754/avb200978030463
  46. 46. Güler H, Calisici O, Bollwein H: Inter- and intra-individual variability of total antioxidant capacity of bovine seminal plasma and relationships with sperm quality before and after cryopreservation. Anim Reprod Sci. 2015, 155:99-105.10.1016/j.anireprosci.2015.02.006
  47. 47. Lindemann CB, O’Brien JA, Giblin FJ: An investigation of effectiveness of certain antioxidants in preserving motility of reactivated bull sperm models. Biol Reprod. 1988, 38:1:114-120.10.1095/biolreprod38.1.114
  48. 48. O’Flaherty CM, Beconi MT, Beorlegui NB: Effect of natural antioxidants superoxide dismutase and hydrogen peroxide on capacitation of frozen-thawed bull spermatozoa. Andrologia 1997, 29:269-275.10.1111/j.1439-0272.1997.tb00481.x
  49. 49. O’Flaherty CM, Beorlegui NB, Beconi MT: Reactive oxygen species requirements for bovine sperm capacitation and acrosome reaction. Theriogenology 1999, 52:2:289-301.10.1016/S0093-691X(99)00129-6
  50. 50. Losano JDA, Angrimani DSR, Rui BR, Bicudo LC, Dalmazzo A, Silva BCS, Viana CHC, Mendes CM, Assumpção MEOA, Barnabe VH, Nichi M: The addition of docosahexaenoic acid (DHA) and antioxidants (glutathione peroxidase and superoxide dismutase) in extenders to epididymal sperm cryopreservation in bulls. Cambrige University Press 2018, 26:3:199-206.10.1017/S0967199418000096
  51. 51. Rajoriya JS, Prasad JK, Ghosh SK, Perumal P, Kumar A, Kaushal S, Singh M: Effects of season changes and cholesterol efflux in relation to freezability in Tharpakar bull semen. Asian Pac J Reprod. 2013, 2:280-288.10.1016/S2305-0500(13)60163-3
  52. 52. Lone SA, Prasad JK, Ghosh SK, Das GK, Balamurugan B, Verma MR: Study on correlation of sperm quality parameters with antioxidant and oxidant status of buffalo bull semen during various stages of cryopreservation. Andrologia 2018, e12970.10.1111/and.1297029430680
  53. 53. Permual P: Effect of superoxide dismutase on semen parameters and antioxidant enzyme activities of liquid stored (50C) Mithun (Bos frontalis) semen. J Anim. 2014, 2014:Article ID 821954, 9 pages.10.1155/2014/821954
  54. 54. Olfati Karaji R, Daghigh Kia H, Ashrafi I: Effects of in combination antioxidant supplementation on microscopic and oxidative parameters of freeze-thaw bull sperm. Cell Tissue Bank 2014, 15:3:461-470.10.1007/s10561-013-9412-y24292238
  55. 55. Luceño NL, Angrimani DSR, Bicudo LC, Szymańska KJ, Poucke MV, Demeyere K, Meyer E, Peelman L, Mullaart E, Broekhuijse MLWJ, Soom AV: Exposing dairy bulls to high temperature-humidity index during spermatogenesis compromises subsequent embryo development in vitro. Theriogenology 2020, 141:16-25.10.1016/j.theriogenology.2019.08.03431494458
  56. 56. Mathevon M, Buhr MM, Dekkers JC: Environmental, management and genetic factors affecting semen production in Holstein bulls. J Dairy Sci. 1998, 81:12:3321-3330.10.3168/jds.S0022-0302(98)75898-9
DOI: https://doi.org/10.2478/acve-2020-0034 | Journal eISSN: 1820-7448 | Journal ISSN: 0567-8315
Language: English
Page range: 453 - 470
Accepted on: Oct 30, 2020
|
Published on: Dec 31, 2020
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year
Related subjects:

© 2020 Petrović Slobodan, Maletić Milan, Lakić Nada, Aleksić Nevenka, Maletić Jelena, Ristanić Marko, Stanimirović Zoran, published by University of Belgrade, Faculty of Veterinary Medicine
This work is licensed under the Creative Commons Attribution 4.0 License.