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Implications of different hypothermic preservation conditions on boar sperm quality during storage: Evaluation in sperm-rich fraction and whole ejaculate

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dc.contributor.author Grudzinska, Paulina
dc.contributor.author Luongo, Chiara
dc.contributor.author Quintero-Moreno, Armando
dc.contributor.author García-Vázquez, Francisco-Alberto
dc.date.accessioned 2026-03-06T14:11:34Z
dc.date.available 2026-03-06T14:11:34Z
dc.date.issued 2025-12
dc.identifier.citation Grudzinska P, Luongo C, Quintero-Moreno A, García-Vázquez FA. Implications of different hypothermic preservation conditions on boar sperm quality during storage: Evaluation in sperm-rich fraction and whole ejaculate. Research in Veterinary Science. diciembre de 2025;197:105936. doi:10.1016/j.rvsc.2025.105936
dc.identifier.issn 0034-5288
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/24696
dc.description.abstract Low-temperature storage of boar semen is a promising alternative to antibiotics in artificial insemination (AI), helping reduce antimicrobial resistance. However, optimal handling protocols remain undefined, especially with the increasing use of semi-automatic collection systems that collect the whole ejaculate (WE) instead of just the sperm-rich fraction (SRF). This study assessed the impact of different temperature conditions on sperm functionality using both SRF and WE samples. Semen doses were refrigerated under four protocols: A) 15 °C for 4 days (15-group); B) 5 °C for 4 days (5-group); C) 5 °C for 2 days then 15 °C until day 4 (5/15-group); D) 15 °C for 2 days then 5 °C until day 4 (15/5-group). Sperm motility, kinematic parameters, plasma membrane and acrosome integrity, and mitochondrial activity were evaluated on days 0, 2, and 4. Thermal stress tests (heat and cold), sperm metabolism (OCR, and ECAR), and IVF outcomes (in WE samples) were assessed on day 4. Sperm quality was slightly affected by storage at 5 °C and by temperature shifts (5/15 °C and 15/5 °C), though values remained within optimal ranges. Thermal stress responses were similar across groups, and quality differences observed during storage disappeared after stress exposure. No significant differences in sperm metabolism were found. While the 15/5-group showed higher penetration rates, all treatments supported IVF. In conclusion, 5 °C storage, alone or combined with 15 °C, preserves sperm function supporting its practical application in AI regardless of ejaculate fraction.
dc.language.iso eng
dc.publisher ELSEVIER SCI LTD
dc.rights Atribución/Reconocimiento 4.0 Internacional
dc.rights.uri https://creativecommons.org/licenses/by/4.0/deed.es
dc.subject.mesh Animals
dc.subject.mesh Male
dc.subject.mesh Semen Preservation/veterinary/methods
dc.subject.mesh Spermatozoa/physiology
dc.subject.mesh Semen Analysis/veterinary
dc.subject.mesh Swine/physiology
dc.subject.mesh Sperm Motility
dc.subject.mesh Cold Temperature
dc.subject.mesh Cryopreservation/veterinary
dc.title Implications of different hypothermic preservation conditions on boar sperm quality during storage: Evaluation in sperm-rich fraction and whole ejaculate
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 41109156
dc.relation.publisherversion https://linkinghub.elsevier.com/retrieve/pii/S0034528825004102
dc.type.version info:eu-repo/semantics/publishedVersion
dc.identifier.doi 10.1016/j.rvsc.2025.105936
dc.journal.title Research in Veterinary Science
dc.identifier.essn 1532-2661


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