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Microencapsulated rrBNGF as an alternative ovulation induction method in rabbits

dc.contributor.authorQuiroga Del Río, Carmen Alejandra
dc.contributor.authorGimeno Martos, Silvia
dc.contributor.authorLorenzo, Pedro L.
dc.contributor.authorArias Álvarez, María
dc.contributor.authorRebollar, Pilar G.
dc.contributor.authorGarcía García, Rosa M.
dc.date.accessioned2025-03-17T16:35:43Z
dc.date.available2025-03-17T16:35:43Z
dc.date.issued2025
dc.descriptionAuthors’ contributions: ACQ, PGR, MAA and RMGG conceived and designed the study. RMGG, MAA, PGR and PL took part in funding acquisition. ACQ wrote the frst draft of the manuscript, and PGR and RMGG shaped the manuscript. ACQ, SGM, PGR and RMGG contributed to experimental collection of data. All authors contributed ideas and substantively revised the manuscript. All authors have read and agreed to the published version of the manuscript.
dc.description.abstractBackground Rabbits are an induced-ovulatory species such that exogenous hormone factors are needed to induce ovulation. Traditionally, intramuscular injections of gonadotropin-releasing hormone (GnRH) analogues are given at the time of artifcial insemination (AI). To avoid the need for injections, the intravaginal delivery of molecules naturally present in seminal plasma has been explored. Here, we examined the possibility of using nerve growth factor (NGF) microencapsulated with chitosan to induce ovulation. First, the biological activity of these NGF microcapsules was assessed in pheochromocytoma of rat adrenal medulla cell (PC12) cultures, along with their efects on semen. Next, we examined the ability of the intravaginal NGF-chitosan delivery system administered at AI (NGFch0) or 30 min before AI (NGFch-30) to elicit ovulation. To this end, progesterone concentrations on Day 7 post AI, pregnancy rates and prolifcacy (kits born alive and stillbirths per doe) were determined in nulliparous and multiparous rabbit does and then compared amongst treatments: intravaginal NGFch-0 and NGFch-30, intramuscular injection of GnRH analogue, intravaginal empty-catheter (C-e) or intravaginal semen-containing catheter (C-s). Results NGF-chitosan promoted similar PC12 diferentiation to free NGF without impairing cell viability. The presence of the NGF-containing microcapsules did not interfere with semen motility, viability or capacitation status. In our in vivo experiments, nulliparous rabbits showed similar rates of ovulating females across treatments (GnRH 90%, NGFch-30 100%, NGFch-0 66.7%, C-e 83.3%), yet higher pregnancy rates were observed in response to GnRH and NGFch-30 (90% and 100%, respectively) than to NGFch-0 (60%). Prolifcacy results in these does were similar across treatments. In multiparous does, GnRH treatment gave rise to the highest rate of ovulating female and pregnancy rates (100 and 90%, respectively). In contrast, the NGF-chitosan groups showed the lowest ovulating female and pregnancy rates (NGFch-30 50% and 25%, NGFch-0 41.7% and 21%, respectively). An intermediate ovulatory response was obtained in does stimulated with the catheter (C-e 70%, C-s 57.1%), and a pregnancy rate of 20% was obtained if the catheter contained diluted semen (C-s). Conclusions Intravaginal NGF-chitosan administered 30 min before AI induced ovulation at a similar rate to GnRH injection in nulliparous, but not multiparous, rabbit females. A better receptivity status of nulliparous females could be a determining factor for this response. However, mechanical stimulation gave rise to a high ovulation rate, so this could be masking or, in some cases, directly replacing the NGF-chitosan efect
dc.description.departmentDepto. de Producción Animal
dc.description.departmentSección Deptal. de Fisiología (Veterinaria)
dc.description.facultyFac. de Veterinaria
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Ciencia, Innovación y Universidades( España)
dc.description.sponsorshipFondo Europeo de Desarrollo Regional (FEDER)
dc.description.sponsorshipUniversidad Complutense de Madrid
dc.description.statuspub
dc.identifier.citationQuiroga, A. C., Gimeno-Martos, S., Lorenzo, P. L., Arias Álvarez, M., G Rebollar, P., & García-García, R. M. (2025). Microencapsulated rrBNGF as an alternative ovulation induction method in rabbits. BMC veterinary research, 21(1), 133. https://doi.org/10.1186/s12917-025-04547-9
dc.identifier.doi10.1186/s12917-025-04547-9
dc.identifier.essn1746-6148
dc.identifier.officialurlhttps://doi.org/10.1186/s12917-025-04547-9
dc.identifier.pmid40025466
dc.identifier.urihttps://hdl.handle.net/20.500.14352/118833
dc.issue.number133
dc.journal.titleBMC Veterinary Research
dc.language.isoeng
dc.page.final14
dc.page.initial1
dc.publisherBioMed Central
dc.relation.projectIDRTI2018-094404-B
dc.relation.projectIDPID2022-138070B
dc.relation.projectID920249
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.cdu636.082.4
dc.subject.keywordChitosan
dc.subject.keywordFertility
dc.subject.keywordNGF
dc.subject.keywordOvulation
dc.subject.keywordPC12 cells
dc.subject.keywordProgesterone
dc.subject.keywordProlificacy
dc.subject.keywordRabbit
dc.subject.keywordSemen
dc.subject.ucmProducción animal
dc.subject.unesco3104 Producción Animal
dc.titleMicroencapsulated rrBNGF as an alternative ovulation induction method in rabbits
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number21(1)
dspace.entity.typePublication
relation.isAuthorOfPublication472ec48e-6ad9-4cfa-944c-4723459e7ba3
relation.isAuthorOfPublicationf0970140-e003-4813-ba43-d0b7a70fb614
relation.isAuthorOfPublication.latestForDiscovery472ec48e-6ad9-4cfa-944c-4723459e7ba3

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Microencapsulated rrBNGF as an alternative ovulation induction method in rabbits

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