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Trends in Rabbit Insemination Extenders for Fresh and Frozen Semen. A Review

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Trends in Rabbit Insemination Extenders for Fresh and Frozen Semen. A Review

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Viudes-De-Castro, MP.; Vicente, JS. (2023). Trends in Rabbit Insemination Extenders for Fresh and Frozen Semen. A Review. World Rabbit Science. 31(2):109-116. https://doi.org/10.4995/wrs.2023.18505

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Título: Trends in Rabbit Insemination Extenders for Fresh and Frozen Semen. A Review
Autor: Viudes-de-Castro, María Pilar Vicente, José Salvador
Entidad UPV: Universitat Politècnica de València. Instituto de Ciencia y Tecnología Animal - Institut de Ciència i Tecnologia Animal
Universitat Politècnica de València. Departamento de Ciencia Animal - Departament de Ciència Animal
Universitat Politècnica de València. Escuela Técnica Superior de Ingeniería Agronómica y del Medio Natural - Escola Tècnica Superior d'Enginyeria Agronòmica i del Medi Natural
Fecha difusión:
Resumen:
[EN] Artificial insemination (AI) has become a popular technique in rabbit farms worldwide. This report discusses the progress made on semen extenders used in rabbit AI, setting out the latest innovations. Fresh and frozen ...[+]
Palabras clave: Artificial insemination , Rabbit , Extender composition
Derechos de uso: Reconocimiento - No comercial - Compartir igual (by-nc-sa)
Fuente:
World Rabbit Science. (issn: 1257-5011 ) (eissn: 1989-8886 )
DOI: 10.4995/wrs.2023.18505
Editorial:
Universitat Politècnica de València
Versión del editor: https://doi.org/10.4995/wrs.2023.18505
Código del Proyecto:
info:eu-repo/grantAgreement/FEDER//IVIA-52201K
info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica, Técnica y de Innovación 2021-2023//PID2021-127867OB-I00/ES/Programa Estatal de Generación de Conocimiento y Fortalecimiento Científico y Tecnológico/
Agradecimientos:
Funding from MCIN/AEI/10.13039/501100011033 and by ERDF, “A way of making Europe” (grant PID2021-127867OB-100), and from GVA-IVIA and the FEDER Operational Program of the Valencian Community, 2021–2027 (grant 52201K) is ...[+]
Tipo: Artículo

References

Abdelnour S.A., Hassan M.A.E., Mohammed A.K., Alhimaidi A.R., Al-Gabri N., Al-Khaldi K.O., Swelum A.A. 2020. The effect of adding different levels of curcumin and its nanoparticles to extender on post-thaw quality of cryopreserved rabbit sperm. Animals, 10: 1508. https://doi.org/10.3390/ani10091508

Abdelnour S.A., Hassan M.A.E., El-Ratel I.T., Essawi W.M., El-Raghi A.A., Lu Y., Sheiha A.M. 2022. Effect of addition of l-carnitine to cryopreservation extender on rabbit post-thaw semen parameters, antioxidant capacity, mitochondrial function, apoptosis and ultrastructure changes. Reprod. Domest. Anim., 57: 902-911. https://doi.org/10.1111/rda.14139

Adams G.P., Ratto M.H., Silva M.E., Carrasco R.A. 2016 Ovulation-inducing factor (OIF/NGF) in seminal plasma: a review and update. Reprod. Dom. Anim., 51: 4-17. https://doi.org/10.1111/rda.12795 [+]
Abdelnour S.A., Hassan M.A.E., Mohammed A.K., Alhimaidi A.R., Al-Gabri N., Al-Khaldi K.O., Swelum A.A. 2020. The effect of adding different levels of curcumin and its nanoparticles to extender on post-thaw quality of cryopreserved rabbit sperm. Animals, 10: 1508. https://doi.org/10.3390/ani10091508

Abdelnour S.A., Hassan M.A.E., El-Ratel I.T., Essawi W.M., El-Raghi A.A., Lu Y., Sheiha A.M. 2022. Effect of addition of l-carnitine to cryopreservation extender on rabbit post-thaw semen parameters, antioxidant capacity, mitochondrial function, apoptosis and ultrastructure changes. Reprod. Domest. Anim., 57: 902-911. https://doi.org/10.1111/rda.14139

Adams G.P., Ratto M.H., Silva M.E., Carrasco R.A. 2016 Ovulation-inducing factor (OIF/NGF) in seminal plasma: a review and update. Reprod. Dom. Anim., 51: 4-17. https://doi.org/10.1111/rda.12795

Amann R.P., Waberski D. 2014. Computer-assited sperm analysis (CASA): capabilities and potential development. Theriogenology, 81: 5-17. https://doi.org/10.1016/j.theriogenology.2013.09.004

Bahar A., Ren D. 2013. Antimicrobial Peptides. Pharmaceuticals, 6: 1543-1575. https://doi.org/10.3390/ph6121543

Bradshaw R.A., Mobley W., Rush R.A. 2017. Nerve growth factor and related substances: A brief history and an introduction to the International NGF Meeting Series. Int. J. Mol. Sci., 18: 1143. https://doi.org/10.3390/ijms18061143

Bromfield J.J. 2016. A role for seminal plasma in modulating pregnancy outcomes in domestic species. Reproduction, 152: R223-32. https://doi.org/10.1530/REP-16-0313

Casares-Crespo L., Vicente J.S., Talaván A.M., Viudesde-Castro M.P. 2016a. Does the inclusion of protease inhibitors in the insemination extender affect rabbit reproductive performance?. Theriogenology, 85: 928-932. https://doi.org/10.1016/j.theriogenology.2015.10.044

Casares-Crespo L., Talaván A.M., Viudes-de-Castro M.P. 2016b. Can the genetic origin affect rabbit seminal plasma protein profile along the year? Reprod. Dom. Anim., 51: 294-300. https://doi.org/10.1111/rda.12680

Casares-Crespo L., Fernández-Serrano P., Vicente J.S., Mocé E., Castellini C., Stabile A.M., Viudes-de-Castro M.P. 2018a. Insemination extender supplementation with bestatin and EDTA has no effect on rabbit reproductive performance. Theriogenology, 105: 61-65. https://doi.org/10.1016/j.theriogenology.2017.09.009

Casares-Crespo L., Fernández-Serrano P., Viudes-de-Castro M.P. 2018b. Protection of GnRH analogue by chitosandextran sulphate nanoparticles for intravaginal application in rabbit artificial insemination. Theriogenology, 116: 49-52. https://doi.org/10.1016/j.theriogenology.2018.05.008

Casares-Crespo L., Fernández-Serrano P., Vicente J.S., Marco-Jiménez F., Viudes-de-Castro M.P. 2018c. Rabbit seminal plasma proteome: The importance of the genetic origin. Anim. Reprod. Sci., 189: 30-42. https://doi.org/10.1016/j.anireprosci.2017.12.004

Casares-Crespo L., Fernández-Serrano P., Viudes-de-Castro M.P. 2019. Proteomic characterization of rabbit (Oryctolagus cuniculus) sperm from two different genotypes. Theriogenology, 128: 140-148. https://doi.org/10.1016/j.theriogenology.2019.01.026

Castellini C. 2008. Semen production and management of rabbit bucks. In Proc.: 9th World Rabbit Congress, 10-13 June, 2008. Verona, Italy.

Castellini C., Lattaioli P., Moroni M.M., Minelli A. 2000. Effect of seminal plasma on the characteristics and fertility of rabbit spermatozoa. Anim. Reprod. Sci., 63: 275-282. https://doi.org/10.1016/s0378-4320(00)00181-0

Castellini C., Mattioli S., Cotozzolo E., Pistilli A., Rende M., Bartolini D., Di Sante G., Menchetti L., Dal Bosco A., Stabile A.M. 2022. The Effect of interaction NGF/p75NTR in sperm cells: a rabbit model. Cells, 11: 1035. https://doi.org/10.3390/cells11061035

Correa A.F., Bastos I.M.D., Neves D., Kipnis A., Junqueira-Kipnis A.P., de Santana J.M. 2017. The activity of a hexameric M17 metallo-aminopeptidase is associated with survival of Mycobacterium tuberculosis. Front. Microbiol., 8: 504. https://doi.org/10.3389/fmicb.2017.00504

Da Costa P.M., Loureiro L., Matos A.J.F. 2013. Transfer of multidrug-resistant bacteria between intermingled ecological niches: the interface between humans, animals and the environment. Int. J. Environ. Res. Public Health, 10: 278-294. https://doi.org/10.3390/ijerph10010278

Dal Bosco A., Rebollar P.G., Boiti C., Zerani M., Castellini C. 2011. Ovulation induction in rabbit does: Current knowledge and perspectives. Anim. Reprod. Sci., 129: 106-117. https://doi.org/10.1016/j.anireprosci.2011.11.007

Dal Bosco A., Cardinali R., Brecchia G., Rebollar P.G., Fatnassi M., Millán P., Mattioli S., Castellini C. 2014. Induction of ovulation in rabbits by adding lecirelin to the seminal dose: In vitro and in vivo effects of different excipients. Anim. Reprod. Sci., 150: 44-49. https://doi.org/10.1016/j.anireprosci.2014.08.009

Dickneite G., Schorlemmer H.U., Hofstaetter T., Sedlacek H.H. 1985. Immunostimulation as a therapeutic principle in bacterial infections: the effect of the immunomodulator bestatin on the experimental chronic E. coli urinary tract infection. In: Harzmann R., Jacobi G.H., Weissbach L. (eds) Experimentelle Urologie. Springer, Berlin, Heidelberg. p. 229-235. https://doi.org/10.1007/978-3-642-70524-3_32

Di Lorio M., Colonna M.A., Miranda M., Principe P., Schiavitto M., Cerolini S., Manchisi A., Iaffaldano N. 2018. Initial cooling time before freezing affects post-thaw quality and reproductive performance of rabbit semen. Anim. Sci. J., 89: 1240-1244. https://doi.org/10.1111/asj.13046

Druart X., Rickard J.P., Mactier S., Kohnke P.L., Kershaw-Young C.M., Bathgate R., Gibb Z., Crossett B., Tsikis G., Labas V., Harichaux G., Grupen C.G., de Graaf S.P. 2013. Proteomic characterization and cross species comparison of mammalian seminal plasma. J. Proteomics, 91: 13-22. https://doi.org/10.1016/j.jprot.2013.05.029

European Food Safety Authority, European Centre for Disease Prevention and Control. 2020. The European Union Summary Report on Antimicrobial Resistance in zoonotic and indicator bacteria from humans, animals and food in 2017/2018. EFSA Journal, 18: 6007.

Fadl A.M., Ghallab A.R.M., Abou-Ahmed M.M., Moawad A.R. 2021. Melatonin can improve viability and functional integrity of cooled and frozen/thawed rabbit spermatozoa. Reprod. Domest. Anim., 56: 103-111. https://doi.org/10.1111/rda.13853.

Fernández-Serrano P., Casares-Crespo L., Viudes-de-Castro M.P. 2017. Chitosan-dextran sulphate nanoparticles for GnRH release in rabbit insemination extenders. Reprod. Domest. Anim. 52: 72-74. https://doi.org/10.1111/rda.13062

Finnegan S., Percival S.L. 2015. EDTA: An antimicrobial and antibiofilm agent for use in wound care. Adv. Wound Care, 4: 415-421. https://doi.org/10.1089/wound.2014.0577

Gil J., Lundeheim N., Söderquist L., Rodríguez-Martínez H. 2003. Influence of extender, temperature, and addition of glycerol on post-thaw sperm parameters in ram semen. Theriogenology, 59: 1241-1255. https://doi.org/10.1016/s0093-691x(02)01177-9

Gogol P. 2016. Reproductive Performance of rabbit does artificially inseminated with semen supplemented with GnRH Analogue [des-Gly10, D-Ala6]-LH-RH Ethylamide. Pol. J. Vet. Sci., 19: 659-661. https://doi.org/10.1515/pjvs-2016-0084

Gupta S., Gabrani R., Ali J., Dang S. 2011. Exploring Novel Approaches to Vaginal Drug Delivery. Recent Pat. Drug Deliv. Formul., 5: 82-84. https://doi.org/10.2174/187221111795471418

Hall S.E., Negus C., Johinke D., Bathgate R. 2017. Adjusting cryodiluent composition for improved post-thaw quality of rabbit spermatozoa. PLoS ONE, 12: e0175965. https://doi.org/10.1371/journal.pone.0175965

Harper G.P., Glanville R.W., Thoenen H. 1982. The purification of nerve growth factor from bovine seminal plasma. Biochemical characterization and partial amino acid sequence. J. Biol. Chem., 257: 8541-8548. https://doi.org/10.1016/S0021-9258(18)34365-5

Holt W.V. 2000. Fundamental aspects of sperm cryobiology: the importance of species and individual differences. Theriogenology, 53: 47-58. https://doi.org/10.1016/s0093-691x(99)00239-3

International Rabbit Reproduction Group. 2005. Guidelines for the handling of rabbit bucks and semen. World Rabbit Sci., 13: 71-91. https://doi.org/10.4995/wrs.2005.527

Jitendra S., Sharma P.K., Bansal S., Banik A. 2011. Noninvasive routes of proteins and peptides drug delivery. Indian J. Pharm. Sci., 73: 367-75. https://doi.org/10.4103/0250-474X.95608

Kershaw-Young C.M., Druart X., Vaughan J., Maxwell W.M. 2012. Beta-nerve growth factor is a major component of alpaca seminal plasma and induces ovulation in female alpacas. Reprod. Fertil. Dev., 24: 1093-1097. https://doi.org/10.1071/RD12039

Kuliková B., Di Iorio M., Kubovicova E., Kuzelova L., Iaffaldano N., Chrenek P. 2014. The cryoprotective effect of Ficoll on the rabbit spermatozoa quality. Zygote, 23: 785-794. https://doi.org/10.1017/S0967199414000471

Kubovicova E., Makarevich A.V., Balazi A., Vasicek J., Chrenek P. 2022. Factors affecting rabbit sperm cryopreservation: a mini-review. Zygote; 30: 1-8. https://doi.org/10.1017/S0967199421000137.

López-Gatius F., Sances G., Sancho M., Yániz J., Santolaria P., Gutiérrez R., Núñez M., Núñez J., Soler C. 2005. Effect of solid storage at 15°C on the subsequent motility and fertility of rabbit semen. Theriogenology, 64: 252-260. https://doi.org/10.1016/j.theriogenology.2004.11.015

Maranesi M., Petrucci L., Leonardi L., Piro F., Rebollar P., Millán P., Cocci P., Vullo C., Parillo F., Moura A., Mariscal G., Boiti C., Zerani M. 2018. New insights on a NGF-mediated pathway to induce ovulation in rabbits (Oryctolagus cuniculus). Biol. Reprod., 98: 634-643. https://doi.org/10.1093/biolre/ioy041

Mahlapuu M., Håkansson J., Ringstad L., Björn C. 2016. Antimicrobial peptides: An emerging category of therapeutic agents. Front. Cell. Infect. Microbiol., 6: 194. https://doi.org/10.3389/fcimb.2016.00194

Marco-Jiménez F., Puchades S., Mocé E., Viudes-de-Castro M.P., Vicente J.S., Rodríguez M. 2004. Use of powdered egg yolk vs. fresh egg yolk for the cryopreservation of ovine semen. Reprod. Dom. Anim., 39: 438-441. https://doi.org/10.1111/j.1439-0531.2004.00537.x

Marco-Jiménez F., Borrás S., Garcia-Dominguez X., D’Auria G., Vicente J.S., Marin C. 2020. Roles of host genetics and sperm microbiota in reproductive success in healthy rabbit. Theriogenology, 158: 416-423. https://doi.org/10.1016/j.theriogenology.2020.09.028

Mattioli S., Maranesi M., Castellini C., Dal Bosco A., Arias-Álvarez M., Lorenzo P.L., Rebollar, P.G., García-García R.M. 2021. Physiology and modulation factors of ovulation in rabbit reproduction management. World Rabbit Sci., 29: 221-229. https://doi.org/10.4995/wrs.2021.13184

Mocé E., Vicente J.S., 2009. Rabbit sperm cryopreservation: A review. Anim. Reprod. Sci. 110: 1–24. https://doi.org/10.1016/j.anireprosci.2008.08.015

Mocé E., Blanch E., Talaván A.M., Viudes-de-Castro M.P. 2014. Reducing the time rabbit sperm are held at 5 °C negatively affects their fertilizing ability after cryopreservation. Theriogenology, 82: 1049-1053. https://doi.org/10.1016/j.theriogenology.2014.07.023

Mocé E., Blanch E., Talaván A.M., Viudes-de-Castro M.P. 2015. Effect of different freezing velocities on the quality and fertilising ability of cryopreserved rabbit spermatozoa. Reprod. Fertil. Develop., 27: 846-851. https://doi.org/10.1071/RD14009

Moretti E., Capitani S., Figura N., Pammolli A., Federico M.G., Giannerini V., Collodel G. 2009. The presence of bacteria species in semen and sperm quality. J. Assist. Reprod. Genet., 26: 47-56. https://doi.org/10.1007/s10815-008-9283-5

Muiño-Blanco T., Pérez-Pé R., Cebrián-Pérez J.A. 2008. Seminal plasma proteins and sperm resistance to stress. Reprod. Dom. Anim., 43: 18-31. https://doi.org/10.1111/j.1439-0531.2008.01228.x

Munari C., Ponzio P., Alkhawagah A.R., Schiavone A., Mugnai C. 2019. Effects of an intravaginal GnRH analogue administration on rabbit reproductive parameters and welfare. Theriogenology, 125: 122-128. https://doi.org/10.1016/j.theriogenology.2018.10.024

Nagy Sz., Sinkovics Gy., Kovács A. 2002. Viability and acrosome integrity of rabbit spermatozoa processed in a gelatinsupplemented extender. Anim. Reprod. Sci., 70: 283-286. https://doi.org/10.1016/S0378-4320(01)00189-0

Nishijima K., Kitajima S., Matsuhisa F., Niimi M., Wang C.C., Fan J. 2021. Strategies for highly efficient rabbit sperm cryopreservation. Animals, 11: 1220. https://doi.org/10.3390/ani11051220

Ondruška L., Parkányi V., Rafay J., Chlebec I. 2008. Effect of LHRH analogue included in seminal dose on kindling rate a prolificacy of rabbits artificially inseminated. 9th World Rabbit Congress, 10-13 June, 2008. Verona, Italy.

Paiva L., Silva M., Carrasco R., Ratto M.H. 2022. The ovulatory and luteotropic actions of the male-derived beta-nerve growth factor in South American camelids. Animal Front., 12: 87-94. https://doi.org/10.1093/af/vfac037

Quintela L.A., Pena A.I., Vega M.D., Gullon J., Prieto M.C., Barrio M., Becerra J.J., Maseda F., Herradón P.G. 2004. Ovulation induction in rabbit does submitted to artificial insemination by adding buserelin to the seminal dose. Reprod. Nutr. Dev., 44: 79-88. https://doi.org/10.1051/rnd:2004015

Quintela L.A., Pena A.I., Vega M.D., Gullon J., Prieto C., Barrio M., Becerra J.J., Herradón P.G. 2009. Reproductive performance of rabbit does artificially inseminated via intravaginal administration of [des-gly 10, D-Ala6]-LHRH ethylamide as ovulation inductor. Reprod. Domest. Anim., 44: 829-833. https://doi.org/10.1111/j.1439-0531.2008.01095.x

Rabea E.I., Badawy M.E.T., Stevens C.V., Smagghe G., Steurbaut W. 2003. Chitosan as antimicrobial agent: Applications and mode of action. Biomacromolecules, 4: 1457-1465. https://doi.org/10.1021/bm034130m

Ratto M.H., Leduc Y.A., Valderrama X.P., van Straaten K.E., Delbaere L.T., Pierson R.A., Adams G.P. 2012. The nerve of ovulationinducing factor in semen. Proc. Natl. Acad. Sci., 109: 15042-15047. https://doi.org/10.1073/pnas.1206273109

Rebollar P.G., Dal Bosco A., Millán P., Cardinali R., Brecchia G., Sylla L., Lorenzo P.L., Castellini C. 2012. Ovulating induction methods in rabbit does: The pituitary and ovarian responses. Theriogenology, 77: 292-298. https://doi.org/10.1016/j.theriogenology.2011.07.041

Rodríguez-Martínez H. 2003. Laboratory semen assessment and prediction of fertility: still utopia?. Reprod. Dom. Anim., 38: 312-318. https://doi.org/10.1046/j.1439-0531.2003.00436.x

Rodríguez-Martínez H., Kvist U., Ernerudh J., Sanz L., Calvete J.J. 2011. Seminal plasma proteins: what role do they play? Am. J. Reprod. Immunol., 66: 11-22. https://doi.org/10.1111/j.1600-0897.2011.01033.x

Rosato M.P., Iaffaldano N. 2011. Effect of chilling temperature on the long-term survival of rabbit spermatozoa held either in a Trisbased or a jellified extender. Reprod. Dom. Anim., 46: 301-308. https://doi.org/10.1111/j.1439-0531.2010.01667.x

Rosato M.P., Iaffaldano N. 2013. Cryopreservation of rabbit semen: Comparing the effects of different cryoprotectants, cryoprotectant free vitrification, and the use of albumin plus osmoprotectants on sperm survival and fertility after standard vapor freezing and vitrification. Theriogenology, 79: 508-516. https://doi.org/10.1016/j.theriogenology.2012.11.008

Rudramurthy G.R., Swamy M.K., Sinniah U.R., Ghasemzadeh A. 2016. Nanoparticles: Alternatives against drugresistant pathogenic microbes. Molecules, 21: 836. https://doi.org/10.3390/molecules21070836

Sahariah P., Másson M. 2017. Antimicrobial chitosan and chitosan derivatives: A review of the structure-activity relationship. Biomacromolecules, 18: 3846-3868. https://doi.org/10.1021/acs.biomac.7b01058

Sánchez-Rodríguez A., Abad P., Arias-Álvarez M., Millán P., Rebollar P.G., Bautista J.M., Lorenzo P.L., García-García R.M. 2019. Recombinant rabbit beta nerve growth factor production and its biological effects on sperm and ovulation in rabbits. PLoS ONE, 14: e0223091. https://doi.org/10.1371/journal.pone.0223091

Trapani A., Lopedota A., Franco M., Cioffi N., Ieva E., García-Fuentes M., Alonso M.J. 2010. A comparative study of chitosan and chitosan/cyclodextrin nanoparticles as potential carriers for the oral delivery of small peptides. Eur. J. Pharm. Biopharm., 75: 26-32. https://doi.org/10.1016/j.ejpb.2010.01.010

Ubeda J.L., Ausejo R., Dahmani Y., Falceto M.V., Usan A., Malo C., Pérez-Martínez F.C. 2013. Adverse effects of members of the Enterobacteriaceae family on boar sperm quality. Theriogenology, 80: 565-570. https://doi.org/10.1016/j.theriogenology.2013.05.022

Vicente J.S., Lavara R., Marco-Jiménez F., Viudes-de-Castro M.P. 2008. Rabbit reproductive performance after insemination with buserelin acetate extender. Livest. Sci., 115: 153-157. https://doi.org/10.1016/j.livsci.2007.07.011

Vicente J.S., Lavara R., Marco-Jiménez F., Viudes-de-Castro M.P. 2011. Detrimental effect on availability of buserelin acetate administered in seminal doses in rabbits. Theriogenology, 76: 1120-1125. https://doi.org/10.1016/j.theriogenology.2011.05.020

Viudes-de-Castro M.P., Lavara R., Marco-Jiménez F., Cortell C., Vicente J.S. 2007. Ovulation induced by mucosa vaginal absorption of buserelin and triptorelin in rabbit. Theriogenology, 68: 1031-1036. https://doi.org/10.1016/j.theriogenology.2007.08.004

Viudes-de-Castro M.P., Mocé E., Lavara R., Marco-Jiménez F., Vicente J.S. 2014a. Aminopeptidase activity in seminal plasma and effect of dilution rate on rabbit reproductive performance after insemination with an extender supplemented with buserelin acetate. Theriogenology, 81: 1223-1228. https://doi.org/10.1016/j.theriogenology.2014.02.003

Viudes-de-Castro M.P., Lavara R., Safaa H.M., Marco-Jiménez F., Mehaisen G.M.K., Vicente J.S. 2014b. Effect of freezing extender composition and male line on semen traits and reproductive performance in rabbits. Animal 8: 765–770. https://doi.org/10.1017/ s1751731114000135.

Viudes-de-Castro M.P., Casares-Crespo L., Marco-Jiménez F., Vicente J.S. 2017. Physical effect of insemination cannula on ovulation induction in rabbit doe. AIDA, XVII Jornadas sobre Producción Animal, Zaragoza, España, 380-382.

Viudes-de-Castro M.P., Marco-Jiménez F., Vicente J.S., Marin C. 2021a. Antibacterial activity of some molecules added to rabbit semen extender as alternative to antibiotics. Animals, 11: 1178. https://doi.org/10.3390/ani11041178

Viudes-de-Castro M.P., Talaván A.G., Vicente J.S. 2021b. Evaluation of dextran for rabbit sperm cryopreservation: Effect on frozen-thawed rabbit sperm quality variables and reproductive performance. Anim. Reprod. Sci., 226: 106714. https://doi.org/10.1016/j.anireprosci.2021.106714

Watson P.F. 2000. The causes of reduced fertility with cryopreserved semen. Anim. Reprod. Sci., 60-61: 481-492. https://doi.org/10.1016/S0378-4320(00)00099-3

Zapletal D., Pavlik A. 2008. The effect of lecirelin (GnRH) dosage on the reproductive performance of nulliparous and lactating rabbit does. Anim. Reprod. Sci., 104: 306-315. https://doi.org/10.1016/j.anireprosci.2007.02.008

Zhang Y.Q., Qin Y. 2012. Reproductive performance of rabbit does by adding leuprorelin in semen to induce ovulation. In Proc.: 10th World Rabbit Congress, 3-6 September, 2012. Sharm El-Sheikh, Egypt.

Zhu Z., Fan X., Lv Y., Zhang N., Fan C., Zhang P., Zeng W. 2015. Vitamin E Analogue Improves Rabbit Sperm Quality during the Process of Cryopreservation through Its Antioxidative Action. PLoS ONE, 10: e0145383. https://doi.org/10.1371/journal.pone.0145383

Zhu Z., Ren Z., Fan X., Pan Y., Lv S., Pan C., Lei A., Zeng W. 2017a. Cysteine protects rabbit spermatozoa against reactive oxygen species-induced damages. PLoS ONE, 12: e0181110. https://doi.org/10.1371/journal.pone.0181110

Zhu Z., Fan X., Lv Y., Lin Y., Wu D., Zeng W. 2017b. Glutamine protects rabbit spermatozoa against oxidative stress via glutathione synthesis during cryopreservation. Reprod. Fertil. Dev., 29: 2183-2194. https://doi.org/10.1071/RD17020.

Zhu Z., Li,R., Lv Y., Zeng W. 2019. Melatonin protects rabbit spermatozoa from cryo-damage via decreasing oxidative stress. Cryobiology, 88: 1-8. https://doi.org/10.1016/j.cryobiol.2019.04.009

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