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Utilisation of sperm‐binding assay combined with computer‐assisted sperm analysis to evaluate frozen‐thawed bull semen

dc.contributor.authorLosano, J. D. A.en_US
dc.contributor.authorAngrimani, D. S. R.en_US
dc.contributor.authorPereira, R. J. G.en_US
dc.contributor.authorRocha, A. M.en_US
dc.contributor.authorCriscuolo, T. S.en_US
dc.contributor.authorBarnabe, V. H.en_US
dc.contributor.authorBarnabe, R. C.en_US
dc.contributor.authorMendes, C. M.en_US
dc.contributor.authorAssumpção, M. E. O. A.en_US
dc.contributor.authorNichi, M.en_US
dc.date.accessioned2015-02-19T15:40:30Z
dc.date.available2016-04-01T15:21:07Zen
dc.date.issued2015-02en_US
dc.identifier.citationLosano, J. D. A.; Angrimani, D. S. R.; Pereira, R. J. G.; Rocha, A. M.; Criscuolo, T. S.; Barnabe, V. H.; Barnabe, R. C.; Mendes, C. M.; Assumpção, M. E. O. A. ; Nichi, M. (2015). "Utilisation of spermâ binding assay combined with computerâ assisted sperm analysis to evaluate frozenâ thawed bull semen." Andrologia 47(1): 77-84.en_US
dc.identifier.issn0303-4569en_US
dc.identifier.issn1439-0272en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/110567
dc.publisherWiley Periodicals, Inc.en_US
dc.publisherIowa State University Pressen_US
dc.subject.othersperm‐binding assayen_US
dc.subject.othersemen analysisen_US
dc.subject.otherperivitelline membraneen_US
dc.subject.otherBullen_US
dc.titleUtilisation of sperm‐binding assay combined with computer‐assisted sperm analysis to evaluate frozen‐thawed bull semenen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelUrologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/110567/1/and12225.pdf
dc.identifier.doi10.1111/and.12225en_US
dc.identifier.sourceAndrologiaen_US
dc.identifier.citedreferenceOliveira LZ, de Arruda RP, de Andrade AFC, Celeghini ECC, Reeb PD, Martins JPN, dos Santos RM, Beletti ME, Peres RFG, Monteiro FM, Hossepian de Lima VFM ( 2013 ) Assessment of in vitro sperm characteristics and their importance in the prediction of conception rate in a bovine timed‐AI program. Anim Reprod Sci 137: 145 – 155.en_US
dc.identifier.citedreferenceKamiguchi Y, Mikamo K ( 1986 ) An improved, efficient method for analyzing human sperm chromosomes using zona‐free hamster ova. Am J Hum Genet 38: 724.en_US
dc.identifier.citedreferenceKoppers AJ, De Iuliis GN, Finnie JM, McLaughlin EA, Aitken RJ ( 2008 ) Significance of mitochondrial reactive oxygen species in the generation of oxidative stress in Spermatozoa. J Clin Endocrinol Metab 93: 3199 – 3207.en_US
dc.identifier.citedreferencede Lamirande E, Cagnon C ( 1993 ) Human sperm hyperactivation and capacitation as parts of an oxidative process. Free Radic Biol Med 14: 157 – 166.en_US
dc.identifier.citedreferencede Lamirande EVE, Tsai C, Harakat A, Gagnon C ( 1998 ) Involvement of reactive oxygen species in human sperm acrosome reaction induced by A23187, lysophosphatidylcholine, and biological fluid ultrafiltrates. J Androl 19: 585 – 594.en_US
dc.identifier.citedreferenceLasley BL, Loskutoff NM, Anderson GB ( 1994 ) The limitation of conventional breeding programs and the need and promise of assisted reproduction in nondomestic species. Theriogenology 41: 119 – 132.en_US
dc.identifier.citedreferenceManjunath P, Nauc V, Bergeron A, Menard M ( 2002 ) Major proteins of bovine seminal plasma bind to the low‐density lipoprotein fraction of hen's egg yolk. Biol Reprod 67: 1250 – 1258.en_US
dc.identifier.citedreferenceMann K ( 2008 ) Proteomic analysis of the chicken egg vitelline membrane. Proteomics 8: 2322 – 2332.en_US
dc.identifier.citedreferenceMukai C, Okuno M ( 2004 ) Glycolysis plays a major role for adenosine triphosphate supplementation in mouse sperm flagellar movement. Biol Reprod 71: 540 – 547.en_US
dc.identifier.citedreferenceNascimento JM, Shi LZ, Tam J, Chandsawangbhuwana C, Durrant B, Botvinick EL, Berns MW ( 2008 ) Comparison of glycolysis and oxidative phosphorylation as energy sources for mammalian sperm motility, using the combination of fluorescence imaging, laser tweezers, and real‐time automated tracking and trapping. J Cell Physiol 217: 745 – 751.en_US
dc.identifier.citedreferenceOhtsuki M, Hanafy AM, Mori M, Sasanami T ( 2004 ) Involvement of interaction of ZP1 and ZPC in the formation of quail perivitelline membrane. Cell Tissue Res 318: 565 – 570.en_US
dc.identifier.citedreferenceParrish JJ, Susko‐Parrish J, Winer MA, First NL ( 1988 ) Capacitation of bovine sperm by heparin. Biol Reprod 38: 1171 – 1180.en_US
dc.identifier.citedreferencePellicer A, Oliveira N, Ruiz A, Remohí J, Simón C ( 1995 ) Exploring the mechanism(s) of endometriosis‐related infertility: an analysis of embryo development and implantation in assisted reproduction. Hum Reprod 10: 91 – 97.en_US
dc.identifier.citedreferencePope CE, Zhang YZ, Dresser BL ( 1991 ) A simple staining method for evaluating acrosomal status of cat spermatozoa. J Zoo Wildlife Med 22: 87 – 95.en_US
dc.identifier.citedreferenceRicker JV, Linfor JJ, Delfino WJ, Kysar P, Scholtz EL, Tablin F, Crowe JH, Ball BA, Meyers SA ( 2006 ) Equine sperm membrane phase behavior: the effects of lipid‐based cryoprotectants. Biol Reprod 74: 359 – 365.en_US
dc.identifier.citedreferenceRobertson L, Brown HL, Staines HJ, Wishart GJ ( 1997 ) Characterization and application of an avian in vitro spermatozoa–egg interaction assay using the inner perivitelline layer from laid chicken eggs. J Reprod Fertil 110: 205 – 211.en_US
dc.identifier.citedreferenceRodler D ( 2011 ) Histochemical detection of glycoconjugates in the inner perivitelline layer of Japanese Quail (Coturnix japonica). Anat Histol Embryol 40: 441 – 449.en_US
dc.identifier.citedreferenceSakkas D, Alvarez JG ( 2010 ) Sperm DNA fragmentation: mechanisms of origin, impact on reproductive outcome, and analysis. Fertil Steril 93: 1027 – 1036.en_US
dc.identifier.citedreferenceSaleh RA, Agarwal A, Nada EA, El‐Tonsy MH, Sharma RK, Meyer A, Nelson DR, Thomas AJ Jr ( 2003 ) Negative effects of increased sperm DNA damage in relation to seminal oxidative stress in men with idiopathic and male factor infertility. Fertil Steril 79: 1597 – 1605.en_US
dc.identifier.citedreferenceShibahara H, Obara H, Ayustawati HY, Suzuki T, Ohno A, Takamizawa S, Suzuki M ( 2004 ) Prediction of pregnancy by intrauterine insemination using CASA estimates and strict criteria in patients with male factor infertility. Int J Androl 27: 63 – 68.en_US
dc.identifier.citedreferenceSt. John JC ( 2002 ) The transmission of mitochondrial DNA following assisted reproductive techniques. Theriogenology 57: 109 – 123.en_US
dc.identifier.citedreferenceStewart SG, Bausek N, Wohlrab F, Schneider WJ, Janet Horrocks A, Wishart GJ ( 2004 ) Species specificity in avian sperm:perivitelline interaction. Comp Biochem Physiol A Mol Integr Physiol 137: 657 – 663.en_US
dc.identifier.citedreferenceTravis AJ, Foster JA, Rosenbaum NA, Visconti PE, Gerton GL, Kopf GS, Moss SB ( 1998 ) Targeting of a germ cell‐specific type 1 hexokinase lacking a porin‐binding domain to the mitochondria as well as to the head and fibrous sheath of murine spermatozoa. Mol Biol Cell 9: 263 – 276.en_US
dc.identifier.citedreferenceVerstegen J, Iguer‐Ouada M, Onclin K ( 2002 ) Computer assisted semen analyzers in andrology research and veterinary practice. Theriogenology 57: 149 – 179.en_US
dc.identifier.citedreferenceWaclawek M, Foisner R, Nimpf J, Schneider WJ ( 1998 ) The chicken homologue of zona pellucida protein‐3 is synthesized by granulosa cells. Biol Reprod 59: 1230 – 1239.en_US
dc.identifier.citedreferenceYanagimachi R ( 1984 ) Zona‐free hamster eggs: their use in assessing fertilizing capacity and examining chromosomes of human spermatozoa. Gamete Res 10: 187 – 232.en_US
dc.identifier.citedreferenceYurewicz EC, Sacco AG, Gupta SK, Xu N, Gage DA ( 1998 ) Hetero‐oligomerization‐dependent binding of pig oocyte zona pellucida glycoproteins ZPB and ZPC to boar sperm membrane vesicles. J Biol Chem 273: 7488 – 7494.en_US
dc.identifier.citedreferenceAitken RJ ( 2006 ) Sperm function tests and fertility. Int J Androl 29: 69 – 75.en_US
dc.identifier.citedreferenceAitken RJ, Paterson M, Fisher H, Buckingham DW, van Duin M ( 1995 ) Redox regulation of tyrosine phosphorylation in human spermatozoa and its role in the control of human sperm function. J Cell Sci 108: 2017 – 2025.en_US
dc.identifier.citedreferenceAitken RJ, Ryan AL, Baker MA, McLaughlin EA ( 2004 ) Redox activity associated with the maturation and capacitation of mammalian spermatozoa. Free Radic Biol Med 36: 994 – 1010.en_US
dc.identifier.citedreferenceAmann RP, Shabanowitz RB, Huszar G, Broder SJ ( 1999 ) In vitro sperm‐binding assay to distinguish differences in populations of human sperm or damage to sperm resulting from cryopreservation. J Androl 20: 648 – 654.en_US
dc.identifier.citedreferenceBarbato GF, Cramer PG, Hammerstedt RH ( 1998 ) A practical in vitro sperm‐egg binding assay that detects subfertile males. Biol Reprod 58: 686 – 699.en_US
dc.identifier.citedreferenceBarratt CL, Tomlinson MJ, Cooke ID ( 1993 ) Prognostic significance of computerized motility analysis for in vivo fertility. Fertil Steril 60: 520 – 525.en_US
dc.identifier.citedreferenceBarth A, Oko R ( 1989 ) Abnormal Morphology of Bovine Spermatozoa. Iowa State University Press, Ames, Iowa.en_US
dc.identifier.citedreferenceBausek N, Waclawek M, Schneider WJ, Wohlrab F ( 2000 ) The major chicken egg envelope protein ZP1 is different from ZPB and is synthesized in the liver. J Biol Chem 275: 28866 – 28872.en_US
dc.identifier.citedreferenceBausek N, Ruckenbauer HH, Pfeifer S, Schneider WJ, Wohlrab F ( 2004 ) Interaction of sperm with purified native chicken ZP1 and ZPC proteins. Biol Reprod 71: 684 – 690.en_US
dc.identifier.citedreferenceBhattacharyya AK, Kanjilal S ( 2003 ) Assessment of sperm functional competence and sperm‐egg interaction. Mol Cell Biochem 253: 255 – 261.en_US
dc.identifier.citedreferenceBonde JPE, Ernst E, Jensen TK, Hjollund NHI, Kolstad H, Scheike T, Giwercman A, Skakkebæk NE, Henriksen TB, Olsen J ( 1998 ) Relation between semen quality and fertility: a population‐based study of 430 first‐pregnancy planners. Lancet 352: 1172 – 1177.en_US
dc.identifier.citedreferenceBurkman LJ, Coddington CC, Franken DR, Krugen TF, Rosenwaks Z, Hogen GD ( 1988 ) The hemizona assay (HZA): development of a diagnostic test for the binding of human spermatozoa to the human hemizona pellucida to predict fertilization potential. Fertil Steril 49: 688 – 697.en_US
dc.identifier.citedreferenceCorcini CD, Silva BE, Brizolara RMR, Gheller SMM, Varela Junior AS, BongalhardoI DC, Lucia Junior T ( 2012 ) Concentração de lactato de cálcio e tempo de incubação sobre a capacidade de adesão e penetração de espermatozoides suínos na membrana perivitelina do ovo da galinha. Ciência Rural 42: 142 – 146.en_US
dc.identifier.citedreferenceCox JF, Alfaro V, Montenegro V, Rodriguez‐Martinez H ( 2006 ) Computer‐assisted analysis of sperm motion in goats and its relationship with sperm migration in cervical mucus. Theriogenology 66: 860 – 867.en_US
dc.identifier.citedreferenceCriscuolo T, Rocha AM, Semaco T, Serzedelo T, Alegretti JR, Serafini P, Motta ELA ( 2010 ) Motile sperm binding to the egg yolk membrane is an easy and feasible function test for acrosome integrity. J Brasileiro Reprod Assist 14: 4.en_US
dc.identifier.citedreferenceFord WCL ( 2006 ) Glycolysis and sperm motility: does a spoonful of sugar help the flagellum go round? Hum Reprod Update 12: 269 – 274.en_US
dc.identifier.citedreferenceGalli C, Lazzari G ( 1996 ) Practical aspects of IVM/IVF in cattle. Anim Reprod Sci 42: 371 – 379.en_US
dc.identifier.citedreferenceGoovaerts IGF, Hoflack GG, Van Soom A, Dewulf J, Nichi M, de Kruif A, Bols PEJ ( 2006 ) Evaluation of epididymal semen quality using the Hamilton–Thorne analyser indicates variation between the two caudae epididymides of the same bull. Theriogenology 66: 323 – 330.en_US
dc.identifier.citedreferenceGraczykowski JW, Francis MM, Paulson RJ, Sokol RZ ( 1998 ) Factors influencing sperm‐zona pellucida binding in vitro using the intact zona model. Hum Reprod 13: 670 – 675.en_US
dc.identifier.citedreferenceGravance CG, Garner DL, Miller MG, Berger T ( 2000 ) Fluorescent probes and flow cytometry to assess rat sperm integrity and mitochondrial function. Reprod Toxicol 15: 5 – 10.en_US
dc.identifier.citedreferenceGriveau JF, Lannou DL ( 1997 ) Reactive oxygen species and human spermatozoa: physiology and pathology. Int J Androl 20: 61 – 69.en_US
dc.identifier.citedreferenceGriveau JF, Renard P, Lannou DL ( 1995 ) Superoxide anion production by human spermatozoa as a part of the ionophore‐induced acrosome reaction process. Int J Androl 18: 67 – 74.en_US
dc.identifier.citedreferenceHalliwell B ( 1999 ) Free Radicals in Biology and Medicine (3rd edn). Oxford University Press, New York, NY.en_US
dc.identifier.citedreferenceHammerstedt RH, Graham JK, Nolan JP ( 1990 ) Cryopreservation of mammalian sperm: what we ask them to survive. J Androl 11: 73.en_US
dc.identifier.citedreferenceHinsch KD, Hinsch E ( 1999 ) The zona pellucida ‘receptors’ ZP1, ZP2 and ZP3. Andrologia 31: 320 – 322.en_US
dc.identifier.citedreferenceHirano Y, Shibahara H, Obara H, Suzuki T, Takamizawa S, Yamaguchi C, Tsunoda H, Sato I ( 2001 ) ANDROLOGY: relationships between sperm motility characteristics assessed by the computer‐aided sperm analysis (CASA) and fertilization rates in vitro. J Assist Reprod Genet 18: 215 – 220.en_US
dc.identifier.citedreferenceHrudka F ( 1987 ) Cytochemical and ultracytochemical demonstration of cytochrome c oxidase in spermatozoa and dynamics of its changes accompanying ageing or induced by stress. Int J Androl 10: 809 – 828.en_US
dc.identifier.citedreferenceIrvine DS, Macleod IC, Templeton AA, Masterton A, Taylor A ( 1994 ) Andrology: a prospective clinical study of the relationship between the computer‐assisted assessment of human semen quality and the achievement of pregnancy in vivo. Hum Reprod 9: 2324 – 2334.en_US
dc.identifier.citedreferenceJeyendran RS, Van der Ven HH, Perez‐Pelaez M, Crabo BG, Zaneveld LJD ( 1984 ) Development of an assay to assess the functional integrity of the human sperm membrane and its relationship to other semen characteristics. J Reprod Fertil 70: 219 – 228.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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