Cryopreservation of sperm in Grey mullet Mugil cephalus (Linnaeus, 1758)
Autor: | Natesan Munuswamy, Ramachandran Balamurugan |
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Rok vydání: | 2017 |
Předmět: |
Male
Cryoprotectant Biology Cryopreservation Dimethylacetamide law.invention chemistry.chemical_compound Endocrinology Food Animals law Freezing Botany Glycerol Animals Sperm motility Chromatography Mugil Extender Fishes 0402 animal and dairy science 04 agricultural and veterinary sciences General Medicine biology.organism_classification Spermatozoa 040201 dairy & animal science Sperm chemistry Sperm Motility 040102 fisheries 0401 agriculture forestry and fisheries Animal Science and Zoology Semen Preservation |
Zdroj: | Animal Reproduction Science. 185:205-213 |
ISSN: | 0378-4320 |
Popis: | The aim of this study was to document the effects of cryopreservation on sperm motility and viability in Grey mullet Mugil cephalus . Cryopreservation of sperm was attempted by using two extenders ringer solution for marine fish (RSMF) and V2 extender (V2E) and cryoprotectants dimethylacetamide (DMA), dimethylsulfoxide (DMSO), ethylene glycol (EG), glycerol (GLY), propylene glycol (PG) and methanol (MeOH). Cryoprotectants were assessed at different concentrations individually as well as in combination with varying equilibration times (10 and 30 min). For optimization of freezing rate, four freezing protocols (−5, −10, −20 and −30 °C/min) were evaluated. After achieving final temperature, samples were plunged in liquid nitrogen (−196 °C) and stored for a week. Samples were subsequently thawed in a water bath at 30 °C for assessment of sperm motility and viability. Results indicated that cryomedium constituting of V2E extender + 10% glycerol with a dilution ratio of 1:1 (sperm: cryomedium) at an equilibration time of 5 to- 10 min and freezing rate of −20 °C/min was more desirable compared with other factors that were assessed. Use of this protocol resulted in retaining the greatest sperm motility grade 3.0 ± 0.0 (50%–80% sperm movement, fast swimming) and 48.19 ± 3.12% of sperm viability. The results of the present study, therefore, provide base-line data for establishing a protocol for sperm cryopreservation in M.cephalus . Further studies are, however, required for optimization of most suitable sperm cryopreservation protocol. |
Databáze: | OpenAIRE |
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