Effect of type and concentration of antioxidant on sperm motility, viability, and DNA integrity of climbing perch Anabas testudineus Bloch, 1792 (Pisces: Anabantidae) post-cryopreservation

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Özet

Sperm quality is preserved through the crucial involvement of antioxidants, which play a vital role in minimizing the occurrence of reactive oxygen species (ROS) during the cryopreservation process. The suitability of the type and concentration of antioxidants are species-dependent, and this study is crucial in order to improve the quality of the climbing perch sperm post-cryopreservation. Therefore, this study aimed to determine the best type and concentration of antioxidants for cryopreservation of climbing perch Anabas testudineus sperm. To achieve this, 6 types of antioxidants, namely, ascorbic acid, beta-carotene, glutathione, butylated hydroxytoluene (BHT), myo-inositol, and alpha-tocopherol, with inclusion of a control were tested in 3 replications at three concentration levels of 0 mg/L (control), 20 mg/L, 40 mg/L, and 60 mg/L. Sperm was diluted in a glucose-base extender at a ratio of 1:60 (sperm: glucose base), then 10 % DMSO and 5 % egg yolk was added before cryopreservation for two weeks. The results showed that the type and concentration of antioxidants had a significant effect on the motility and viability of cryopreserved climbing perch sperm (P < 0.05), where the best results for ascorbic acid, beta-carotene, glutathione, myo-inositol, and alpha-tocopherol were obtained at a concentration of 60 mg/L, while BHT was at a concentration of 20 mg/L. The best results for glutathione, myo-inositol, and alpha-tocopherol were significantly different from other treatments, while the best results for ascorbic acid and beta-carotene (60 mg/L) were not significantly different from the 40 mg/L concentration, while the best results for BHT were not significantly different from the control treatments. Therefore, the best concentration of glutathione, myo-inositol, and alpha-tocopherol was 60 mg/L, while for ascorbic acid and beta-carotene it was 40 mg/L, and BHT was not recommended. DNA integrity analysis indicated the absence of fragmentation in all samples, including fresh, control, and treated sperm. Based on practical and economic considerations, myo-inositol at 60 mg/L was recommended for cryopreservation of climbing perch A. testudineus sperm.

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dc.contributor.authorMaulida, Siti
dc.contributor.authorEriani, Kartini
dc.contributor.authorFadli, Nur
dc.contributor.authorSiti-Azizah, Mohd N.
dc.contributor.authorKocabas, Filiz K.
dc.contributor.authorKocabas, Mehmet
dc.contributor.authorWilkes, Martin
dc.contributor.authorHandayani, Luvi S.
dc.contributor.authorRahayu, Sri R.
dc.contributor.authorMuchlisin, Zainal A.
dc.date.accessioned2026-10-28T14:54:26.020566153Z
dc.date.available2026-10-28T14:54:26.020566153Z
dc.date.issued2024
dc.description.abstractSperm quality is preserved through the crucial involvement of antioxidants, which play a vital role in minimizing the occurrence of reactive oxygen species (ROS) during the cryopreservation process. The suitability of the type and concentration of antioxidants are species-dependent, and this study is crucial in order to improve the quality of the climbing perch sperm post-cryopreservation. Therefore, this study aimed to determine the best type and concentration of antioxidants for cryopreservation of climbing perch Anabas testudineus sperm. To achieve this, 6 types of antioxidants, namely, ascorbic acid, beta-carotene, glutathione, butylated hydroxytoluene (BHT), myo-inositol, and alpha-tocopherol, with inclusion of a control were tested in 3 replications at three concentration levels of 0 mg/L (control), 20 mg/L, 40 mg/L, and 60 mg/L. Sperm was diluted in a glucose-base extender at a ratio of 1:60 (sperm: glucose base), then 10 % DMSO and 5 % egg yolk was added before cryopreservation for two weeks. The results showed that the type and concentration of antioxidants had a significant effect on the motility and viability of cryopreserved climbing perch sperm (P < 0.05), where the best results for ascorbic acid, beta-carotene, glutathione, myo-inositol, and alpha-tocopherol were obtained at a concentration of 60 mg/L, while BHT was at a concentration of 20 mg/L. The best results for glutathione, myo-inositol, and alpha-tocopherol were significantly different from other treatments, while the best results for ascorbic acid and beta-carotene (60 mg/L) were not significantly different from the 40 mg/L concentration, while the best results for BHT were not significantly different from the control treatments. Therefore, the best concentration of glutathione, myo-inositol, and alpha-tocopherol was 60 mg/L, while for ascorbic acid and beta-carotene it was 40 mg/L, and BHT was not recommended. DNA integrity analysis indicated the absence of fragmentation in all samples, including fresh, control, and treated sperm. Based on practical and economic considerations, myo-inositol at 60 mg/L was recommended for cryopreservation of climbing perch A. testudineus sperm.
dc.description.sponsorshipMinistry of Education, Culture, Research, and Technology of Republic of Indonesia
dc.identifier.articlenumber104851
dc.identifier.doi10.1016/j.cryobiol.2024.104851
dc.identifier.eissn1090-2392
dc.identifier.issn0011-2240
dc.identifier.pmid38237749
dc.identifier.scopus2-s2.0-85182788436
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/munzur/1640
dc.identifier.volume114
dc.identifier.wosWOS:001167999700001
dc.language.isoen
dc.publisherAcademic Press Inc.
dc.relation.ispartofCryobiology
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectDMSO
dc.subjectDNA integrity
dc.subjectGlucose base
dc.subjectGlutathione
dc.subjectMyo-inositol
dc.subject.otheralpha-Tocopherol
dc.subject.otherAnimals
dc.subject.otherAntioxidants
dc.subject.otherAscorbic Acid
dc.subject.otherbeta Carotene
dc.subject.otherCryopreservation
dc.subject.otherDNA
dc.subject.otherGlucose
dc.subject.otherGlutathione
dc.subject.otherInositol
dc.subject.otherMale
dc.subject.otherPerches
dc.subject.otherSemen
dc.subject.otherSemen Preservation
dc.subject.otherSperm Motility
dc.subject.otherSpermatozoa
dc.subject.otheralpha tocopherol
dc.subject.otherbutylcresol
dc.subject.othercryoprotective agent
dc.subject.otherdimethyl sulfoxide
dc.subject.otherimmunoglobulin Y
dc.subject.otherantioxidant
dc.subject.otherAnabas testudineus
dc.subject.otheranimal cell
dc.subject.otheranimal experiment
dc.subject.otherantioxidant assay
dc.subject.otherArticle
dc.subject.otherconcentration (parameter)
dc.subject.othercontrolled study
dc.subject.otherdilution
dc.subject.otherDNA determination
dc.subject.otherDNA fragmentation
dc.subject.otherDNA integrity
dc.subject.otherDNA replication
dc.subject.othereconomic aspect
dc.subject.otheregg yolk
dc.subject.othergenetic parameters
dc.subject.othernonhuman
dc.subject.othersample
dc.subject.othersperm
dc.subject.othersperm quality
dc.subject.othersperm viability
dc.subject.otherspermatozoon motility
dc.subject.otheranimal
dc.subject.otherperch
dc.subject.otherprocedures
dc.subject.othersperm preservation
dc.subject.otherspermatozoon
dc.subject.otherveterinary medicine
dc.titleEffect of type and concentration of antioxidant on sperm motility, viability, and DNA integrity of climbing perch Anabas testudineus Bloch, 1792 (Pisces: Anabantidae) post-cryopreservation
dc.typeArticle
rdl.citation.openalex12
rdl.citation.scopus19
rdl.departmentGraduate School of Mathematics and Applied Sciences, Universitas Syiah Kuala, Banda Aceh, 23111, Indonesia
rdl.departmentDepartment of Aquaculture, Faculty of Marine and Fisheries, Universitas Syiah Kuala, Banda Aceh, 23111, Indonesia
rdl.departmentDepartment of Biology, Faculty of Mathematics and Natural Sciences, Universitas Syiah Kuala, Banda Aceh, 23111, Indonesia
rdl.departmentInstitute of Climate Adaptation and Marine Biotechnology, Universiti Malaysia Terengganu, Kuala Terengganu, Malaysia
rdl.departmentFaculty of Fisheries, Munzur University, Turkey
rdl.departmentDepartment of Wildlife Ecology and Management, Karadeniz Technical University, Turkey
rdl.departmentSchool of Life Sciences, University of Essex, Colchester, UK
rdl.oa.statusclosed
rdl.scopus.quartileQ2
rdl.sdgSDG02
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED