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

dc.contributor.authorKoca, Recep Hakkı
dc.contributor.authorGüngör, İbrahim Halil
dc.contributor.authorCihangiroğlu, Aslıhan Çakır
dc.contributor.authorAcısu, Tutku Can
dc.contributor.authorBadıllı, Nida
dc.contributor.authorAkarsu, Serkan Ali
dc.contributor.authorKaya, Şeyma Özer
dc.contributor.authorKaya, Emre
dc.contributor.authorTürk, Gaffari
dc.contributor.authorSönmez, Mustafa
dc.contributor.authorGür, Seyfettin
dc.date.accessioned2025-07-08T05:32:38Z
dc.date.available2025-07-08T05:32:38Z
dc.date.issued2025-07
dc.departmentFakülteler, Veteriner Fakültesi, Klinik Bilimler Bölümü
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 µM mitoTEMPO with 3% glycerol, 1 µM mitoTEMPO with 5% glycerol, 5 µM mitoTEMPO with 3% glycerol and 5 µM 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 µM 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.identifier.doi10.1002/vms3.70406
dc.identifier.issue4
dc.identifier.other40587514
dc.identifier.pmid40587514
dc.identifier.scopus2-s2.0-105009862191
dc.identifier.scopusqualityN/A
dc.identifier.urihttps://doi.org/10.1002/vms3.70406
dc.identifier.urihttps://hdl.handle.net/20.500.12604/8751
dc.identifier.volume11
dc.identifier.wosWOS:001519874200001
dc.identifier.wosqualityQ2
dc.indekslendigikaynakPubMed
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.institutionauthorCihangiroğlu, Aslıhan Çakır
dc.language.isoen
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectDNA fragmentation
dc.subjectcryopreservation
dc.subjectmitoTEMPO
dc.subjectram
dc.subjectsemen
dc.subjectDNA fragmentation
dc.subjectcryopreservation
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.typeOther

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