Optimization of sperm cryopreservation protocol for Basa catfish (Pangasius bocourti).

Cryobiology

College of Food Science and Technology, Guangdong Ocean University (Yangjiang Campus), Yangjiang, 529500, China. Electronic address:

Published: June 2023

AI Article Synopsis

  • The study focused on optimizing sperm cryopreservation for Basa catfish, exploring factors like cryoprotectants, thawing conditions, and storage times.
  • The best results were found using 10% propylene glycol as a cryoprotectant, and thawing at 30-40°C significantly increased sperm motility post-thaw.
  • The research concluded that optimized pre-freezing and thawing conditions allow for successful cryopreservation, enabling effective artificial reproduction without significant differences in fertilization rates compared to fresh sperm.

Article Abstract

The aim of this study was to optimize a sperm cryopreservation protocol for Basa catfish (Pangasius bocourti). Key factors for the efficiency of cryopreservation, including cryoprotectants, thawing conditions, equilibration times, dilution ratios and freezing methods, were investigated. The suitable time for post-thaw storage as well as pre-freezing cool storage was also examined. Five cryoprotectants (dimethyl sulfoxide, MeSO; dimethylformamide, DMF; ethylene glycol, EG; propylene glycol, PG; N-methylacetamide, MA) at different final concentrations (5, 10 and 15%) were tested, 10% PG provided the best cryoprotective effect. Thawing temperature at 30-40 °C yielded significantly higher post-thaw motility than 20, 25, 50 or 60 °C. No obvious effect on sperm motility was detected either in equilibrated or thawed samples during a 2-h equilibration. Regarding dilution ratio (semen/cryomedium, v/v), percentage of motile spermatozoa was significantly higher at ratios of 2:1, 1:1 and 1:3 than those with higher ratios (1:5, 1:7 and 1:9). Thawed sperm was sensitive to post-thaw storage, but no reduction in motility was detected within 30 min. Further evaluation of the effective pre-freezing storage time indicated that sperm in diluted form had more advantage in maintaining its freezability, which could be chilled for 24 h before freezing without compromising post-thaw sperm motility. P. bocourti sperm could be successfully cryopreserved with both a programmable freezer and the floating frame technique (frozen 5 or 7 cm above the surface of liquid nitrogen). Cryopreserved sperm (77.5 ± 5.1%) fertilization was not significantly different from fresh sperm (80.9 ± 4.7%) at the ratio of 2 × 10 spermatozoa per egg. Our results provided more detailed suitable conditions for P. bocourti sperm cryopreservation than previous studies. Standardizing the cryopreservation protocol and storage time would be helpful in facilitating artificial reproduction in this species.

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http://dx.doi.org/10.1016/j.cryobiol.2023.04.001DOI Listing

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