Optimizing Cryopreservation: The Effect of MitoTEMPO and Glycerol Ratios on Ram Semen Quality After Freezing and Thawing

dc.contributor.authorKoca, Recep Hakki
dc.contributor.authorGungor, Ibrahim Halil
dc.contributor.authorCihangiroglu, Aslihan cakir
dc.contributor.authorAcisu, Tutku Can
dc.contributor.authorBadilli, Nida
dc.contributor.authorAkarsu, Serkan Ali
dc.contributor.authorGur, Seyfettin
dc.date.accessioned2026-08-12T17:26:55Z
dc.date.issued2025
dc.departmentFırat Üniversitesi
dc.description.abstractBackground: MitoTEMPO is an important mitochondrial targeted and ROS scavenging antioxidant. It is often used as antiviral, anticancer and immunomodulator agents. In addition, there are studies proving its positive effect on sperm after thawing. Objectives: The aim of our study was to determine the effects of mitoTEMPO addition, which has strong antioxidant and cryoprotective properties in different glycerol ratios, on motility, kinematics, sperm quality and oxidative stress in spermatozoa after freezing and thawing. Materials and Methods: Semen was collected from seven rams twice a week for 3 weeks. The semen samples were pooled and extended using standard protocol. Experimental groups were formed (1 mu M mitoTEMPO with 3% glycerol, 1 mu M mitoTEMPO with 5% glycerol, 5 mu M mitoTEMPO with 3% glycerol and 5 mu M mitoTEMPO with 5% glycerol) and without (control with 3% glycerol and control with 5% glycerol) mitoTEMPO and they were frozen in mini straws. In this study, motility, kinematic parameters, plasma membrane integrity, mitochondrial membrane potential, acrosome integrity, viability, DNA fragmentation and oxidative stress parameters were determined. Results: The increases in total motility, increases in plasma membrane integrity ratio, decreases in MDA level and decreases in DNA damage ratio in mitoTEMPO groups were statistically significant (p < 0.05). Conclusion: Post-thawed sperm, the addition of 1 M mitoTEMPO to the 3% glycerol extender preserved the integrity of the spermatozoon membrane, increased total motility, prevented DNA damage and oxidative stress, and increased the rate of sperm with intact acrosome.
dc.description.sponsorshipScientific and Technological Research Council of Turkey [120O011]
dc.description.sponsorshipThis study was supported by The Scientific and Technological Research Council of Turkey, Grant no: 120O011.
dc.identifier.doi10.1002/vms3.70406
dc.identifier.issn2053-1095
dc.identifier.issue4
dc.identifier.orcid0000-0002-0882-937X
dc.identifier.orcid0000-0002-7445-3091
dc.identifier.orcid0000-0003-4450-6540
dc.identifier.orcid0000-0002-1740-8016
dc.identifier.pmid40587514
dc.identifier.scopus2-s2.0-105009862191
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1002/vms3.70406
dc.identifier.urihttps://hdl.handle.net/11508/55015
dc.identifier.volume11
dc.identifier.wosWOS:001519874200001
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofVeterinary Medicine and Science
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260511
dc.subjectcryopreservation
dc.subjectDNA fragmentation
dc.subjectmitoTEMPO
dc.subjectram
dc.subjectsemen
dc.titleOptimizing Cryopreservation: The Effect of MitoTEMPO and Glycerol Ratios on Ram Semen Quality After Freezing and Thawing
dc.typeArticle

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