Effect of genistein addition to equine sperm freezing extender
Abstract
ΔΕΝ ΥΠΑΡΧΕΙ ΠΕΡΙΛΗΨΗ
Article Details
- Zitationsvorschlag
-
MACÍAS-GARCÍA Β., GUIMARÃES Τ., LOPES, G., ROCHA, A., & GONZÁLEZ-FERNÁNDEZ, L. (2018). Effect of genistein addition to equine sperm freezing extender. Journal of the Hellenic Veterinary Medical Society, 66(4), 241–248. https://doi.org/10.12681/jhvms.15868
- Ausgabe
- Bd. 66 Nr. 4 (2015)
- Rubrik
- Research Articles
Dieses Werk steht unter der Lizenz Creative Commons Namensnennung - Nicht-kommerziell 4.0 International.
Authors who publish with this journal agree to the following terms:
· Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution Non-Commercial License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
· Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g. post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
· Authors are permitted and encouraged to post their work online (preferably in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work.
Downloads
Keine Nutzungsdaten vorhanden.
Literaturhinweise
Aitken RJ, Baker MA (2006) Oxidative stress, sperm survival and fertility control. Mol Cell Endocrinol 250:66-69.
Bailey JL, Bilodeau JF, Cormier N (2000) Semen cryopreservation in domestic animals: a damaging and capacitating phenomenon. J Androl 21:1-7.
Ball BA, Vo A (2002) Detection of lipid peroxidation in equine spermatozoa based upon the lipophilic fluorescent dye C1l-BODIPY581/591. J Androl 23:259-269.
Ball BA, Vo AT, Baumber J (2001) Generation of reactive oxygen species by equine spermatozoa. Am J Vet Res 62:508-515.
Baumber J, Ball BA, Gravance CG, Medina V, vies-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.
Baumber J, Ball BA, Linfor JJ (2005) Assessment of the cryopreservation of equine spermatozoa in the presence of enzyme scavengers and antioxidants. Am J Vet Res 66:772-779.
Baumber J, Ball BA, Linfor JJ, Meyers SA (2003a) Reactive oxygen species and cryopreservation promote DNA fragmentation in equine spermatozoa. J Androl 24:621-628.
Baumber J, Sabeur K, Vo A, Ball BA (2003b) Reactive oxygen species promote tyrosine phosphorylation and capacitation in equine spermatozoa. Theriogenology 60:1239-1247.
Burnaugh L, Ball BA, Sabeur K, Thomas AD, Meyers SA (2010) Osmotic stress stimulates generation of superoxide anion by spermatozoa in horses. Anim Reprod Sci 117:249-260.
Cormier N, Bailey JL (2003) A differential mechanism is involved during heparin- and cryopreservation-induced capacitation of bovine spermatozoa. Biol Reprod 69:177-185.
De Andrade AF, Zaffalon FG, Celeghini EC, Nascimento J, Bressan FF, Martins SM, de Arruda RP (2012) Post-thaw addition of seminal plasma reduces tyrosine phosphorylation on the surface of cryopreserved equine sperm, but does not reduce lipid peroxidation. Theriogenology 77:1866-1872.
de Lamirande E, Jiang H, Zini A, Kodama H, Gagnon C (1997) Reactive oxygen species and sperm physiology. Rev Reprod 2:48-54.
de Oliveira RA, Wolf CA, de Oliveira Viu MA, Gambarini ML (2013) Addition of Glutathione to an Extender for Frozen Equine Semen. J Equine Vet Sci 33:1148-1152.
Garcia BM, Fernandez LG, Ferrusola CO, Salazar-Sandoval C, Rodriguez AM, Martinez HR, Tapia JA, Morcuende D, Pena FJ (2011) Membrane lipids of the stallion spermatozoon in relation to sperm quality and susceptibility to lipid peroxidation. Reprod Domest Anim 46:141-148.
Gibb Z, Butler TJ, Morris LH, Maxwell WM, Grupen CG (2013) Quercetin improves the postthaw characteristics of cryopreserved sex-sorted and nonsorted stallion sperm. Theriogenology 79:1001-1009.
González-Fernández L, Macías-García B, Loux SC, Varner DD, Hinrichs K (2013) Focal adhesion kinases and calcium/calmodulin-dependent protein kinases regulate protein tyrosine phosphorylation in stallion sperm. Biol Reprod 88:138.
González-Fernández L, Macías-García B, Velez IC, Varner DD, Hinrichs K (2012a) Calcium-calmodulin and pH regulate protein tyrosine phosphorylation in stallion sperm. Reproduction 144:411-422.
González-Fernández L, Morrell JM, Pena FJ, Macías-García B (2012b) Osmotic shock induces structural damage on equine spermatozoa plasmalemma and mitochondria. Theriogenology 78:415-422.
Guimarães T, Lopes G, Ferreira P, Leal I, Rocha A (2012) Characteristics of stallion epididymal spermatozoa at collection and effect of two refrigeration protocols on the quality of the frozen/thawed sperm cells. Anim Reprod Sci 6:85-89.
Hammerstedt RH, Graham JK, Nolan JP (1990) Cryopreservation of mammalian sperm: what we ask them to survive. J Androl 11:73-88.
Loomis PR, Graham JK (2008) Commercial semen freezing: individual male variation in cryosurvival and the response of stallion sperm to customized freezing protocols. Anim Reprod Sci 105 119-128.
Martorana K, Klooster K, Meyers S (2014) Suprazero cooling rate, rather than freezing rate, determines post thaw quality of rhesus macaque sperm. Theriogenology 81:381-388.
Menzel VA, Hinsch E, Hagele W, Hinsch KD (2007) Effect of genistein on acrosome reaction and zona pellucida binding independent of protein tyrosine kinase inhibition in bull. Asian J Androl 9 650-658.
Metcalf ES (2007) The efficient use of equine cryopreserved semen. Theriogenology 68:423-428.
Morillo-Rodriguez A, Macías-García B, Tapia JA, Ortega-Ferrusola C, Pena FJ (2012) Consequences of butylated hydroxytoluene in the freezing extender on post-thaw characteristics of stallion spermatozoa in vitro. Andrologia 44 Suppl 1 688-695.
Parker NA, Bailey TL, Bowen JM, Ley WB, Purswell BJ, Dascanio JJ (2000) In vitro and xenogenous capacitation-like changes of fresh, cooled, and cryopreserved stallion sperm as assessed by a chlortetracycline stain. J Androl 21:45-52.
Pommer AC, Rutllant J, Meyers SA (2002) The role of osmotic resistance on equine spermatozoal function. Theriogenology 58:1373-1384.
Pommer AC, Rutllant J, Meyers SA (2003) Phosphorylation of protein tyrosine residues in fresh and cryopreserved stallion spermatozoa under capacitating conditions. Biol Reprod 68:1208-1214.
Record IR, Dreosti IE, Mcinerney JK (1995) The Antioxidant Activity of Genistein In-Vitro. J of Nutr Bioch 6:481-485.
Schembri MA, Major DA, Suttie JJ, Maxwell WM, Evans G (2002) Capacitation-like changes in equine spermatozoa throughout the cryopreservation process. Reprod Fertil Dev 14:225-233.
Sieme H, Harrison RA, Petrunkina AM (2008) Cryobiological determinants of frozen semen quality, with special reference to stallion. Anim Reprod Sci 107:276-292.
Silva PF, Gadella BM (2006) Detection of damage in mammalian sperm cells. Theriogenology 65:958-978.
Thomas AD, Meyers SA, Ball BA (2006) Capacitation-like changes in equine spermatozoa following cryopreservation. Theriogenology 65:1531-1550.
Thomson LK, Fleming SD, Aitken RJ, De Iuliis GN, Zieschang JA, Clark AM (2009) Cryopreservation-induced human sperm DNA damage is predominantly mediated by oxidative stress rather than apoptosis. Hum Reprod 24:2061-2070.
Visconti PE, Bailey JL, Moore GD, Pan D, Olds-Clarke P, Kopf GS (1995) Capacitation of mouse spermatozoa. I. Correlation between the capacitation state and protein tyrosine phosphorylation. Development 121:1129-1137.
