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
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.
Anahtar Kelimeler
- Scopus
- 19
- OpenAlex
- 12
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Maulida, Siti | |
| dc.contributor.author | Eriani, Kartini | |
| dc.contributor.author | Fadli, Nur | |
| dc.contributor.author | Siti-Azizah, Mohd N. | |
| dc.contributor.author | Kocabas, Filiz K. | |
| dc.contributor.author | Kocabas, Mehmet | |
| dc.contributor.author | Wilkes, Martin | |
| dc.contributor.author | Handayani, Luvi S. | |
| dc.contributor.author | Rahayu, Sri R. | |
| dc.contributor.author | Muchlisin, Zainal A. | |
| dc.date.accessioned | 2026-10-28T14:54:26.020566153Z | |
| dc.date.available | 2026-10-28T14:54:26.020566153Z | |
| dc.date.issued | 2024 | |
| dc.description.abstract | 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. | |
| dc.description.sponsorship | Ministry of Education, Culture, Research, and Technology of Republic of Indonesia | |
| dc.identifier.articlenumber | 104851 | |
| dc.identifier.doi | 10.1016/j.cryobiol.2024.104851 | |
| dc.identifier.eissn | 1090-2392 | |
| dc.identifier.issn | 0011-2240 | |
| dc.identifier.pmid | 38237749 | |
| dc.identifier.scopus | 2-s2.0-85182788436 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/munzur/1640 | |
| dc.identifier.volume | 114 | |
| dc.identifier.wos | WOS:001167999700001 | |
| dc.language.iso | en | |
| dc.publisher | Academic Press Inc. | |
| dc.relation.ispartof | Cryobiology | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.subject | DMSO | |
| dc.subject | DNA integrity | |
| dc.subject | Glucose base | |
| dc.subject | Glutathione | |
| dc.subject | Myo-inositol | |
| dc.subject.other | alpha-Tocopherol | |
| dc.subject.other | Animals | |
| dc.subject.other | Antioxidants | |
| dc.subject.other | Ascorbic Acid | |
| dc.subject.other | beta Carotene | |
| dc.subject.other | Cryopreservation | |
| dc.subject.other | DNA | |
| dc.subject.other | Glucose | |
| dc.subject.other | Glutathione | |
| dc.subject.other | Inositol | |
| dc.subject.other | Male | |
| dc.subject.other | Perches | |
| dc.subject.other | Semen | |
| dc.subject.other | Semen Preservation | |
| dc.subject.other | Sperm Motility | |
| dc.subject.other | Spermatozoa | |
| dc.subject.other | alpha tocopherol | |
| dc.subject.other | butylcresol | |
| dc.subject.other | cryoprotective agent | |
| dc.subject.other | dimethyl sulfoxide | |
| dc.subject.other | immunoglobulin Y | |
| dc.subject.other | antioxidant | |
| dc.subject.other | Anabas testudineus | |
| dc.subject.other | animal cell | |
| dc.subject.other | animal experiment | |
| dc.subject.other | antioxidant assay | |
| dc.subject.other | Article | |
| dc.subject.other | concentration (parameter) | |
| dc.subject.other | controlled study | |
| dc.subject.other | dilution | |
| dc.subject.other | DNA determination | |
| dc.subject.other | DNA fragmentation | |
| dc.subject.other | DNA integrity | |
| dc.subject.other | DNA replication | |
| dc.subject.other | economic aspect | |
| dc.subject.other | egg yolk | |
| dc.subject.other | genetic parameters | |
| dc.subject.other | nonhuman | |
| dc.subject.other | sample | |
| dc.subject.other | sperm | |
| dc.subject.other | sperm quality | |
| dc.subject.other | sperm viability | |
| dc.subject.other | spermatozoon motility | |
| dc.subject.other | animal | |
| dc.subject.other | perch | |
| dc.subject.other | procedures | |
| dc.subject.other | sperm preservation | |
| dc.subject.other | spermatozoon | |
| dc.subject.other | veterinary medicine | |
| dc.title | 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 | |
| dc.type | Article | |
| rdl.citation.openalex | 12 | |
| rdl.citation.scopus | 19 | |
| rdl.department | Graduate School of Mathematics and Applied Sciences, Universitas Syiah Kuala, Banda Aceh, 23111, Indonesia | |
| rdl.department | Department of Aquaculture, Faculty of Marine and Fisheries, Universitas Syiah Kuala, Banda Aceh, 23111, Indonesia | |
| rdl.department | Department of Biology, Faculty of Mathematics and Natural Sciences, Universitas Syiah Kuala, Banda Aceh, 23111, Indonesia | |
| rdl.department | Institute of Climate Adaptation and Marine Biotechnology, Universiti Malaysia Terengganu, Kuala Terengganu, Malaysia | |
| rdl.department | Faculty of Fisheries, Munzur University, Turkey | |
| rdl.department | Department of Wildlife Ecology and Management, Karadeniz Technical University, Turkey | |
| rdl.department | School of Life Sciences, University of Essex, Colchester, UK | |
| rdl.oa.status | closed | |
| rdl.scopus.quartile | Q2 | |
| rdl.sdg | SDG02 | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | PUBMED |

