Literature DB >> 11245263

Quality control of refrigerated and cryopreserved semen using computer-assisted sperm analysis (CASA), viable staining and standardized fertilization in African catfish (Clarias gariepinus).

E Rurangwa1, F A Volckaert, G Huyskens, D E Kime, F Ollevier.   

Abstract

A new integrated approach including computer-assisted sperm analysis (CASA), viability staining and fertilization was used to study the quality of cryodiluents used in fish sperm cryopreservation. As an example the sperm quality of an African catfish, Clarias gariepinus (Burchell, 1822), was assessed by its fertilizing ability, motility and viability at day 0 (fresh), after 2 days' storage at 4 degreesC and after 2 days, 5 months and 10 months frozen at -196 degreesC using solutions containing dimethyl sulphoxide (DMSO) or glycerol as permeating cryoprotectants. Four of the best freezing solutions were used, namely, Steyn's extender (S1, S4) and Mounib's extender (M3, M4) associating 10% hen's egg yolk. Progressive sperm movement measured by CASA and expressed by the straight line velocity (VSL), the average path velocity (VAP) and the curvilinear velocity (VCL) was highly correlated with hatching rates obtained from fertilization using minimal sperm:egg ratios. After 2 days, the motility of spermatozoa frozen with DMSO and 10% egg yolk had deteriorated less than that of spermatozoa stored at 4 degreesC. Post-thaw hatching rates reflected the post-thaw sperm viability, which was cryodiluent dependent: 14.9+/-2.0% (S4), 17.0+/-4.2% (S1), 25.9+/-3.7% (M4) and 52.1+/-3.4% (M3) after 5 months of cryopreservation. The percent motility of 10-months-frozen spermatozoa was high in M3 (70.7+/-11.4%) and M4 (64.0+/-2.0%) cryoprotected sperm when measured between 5 and 20 sec after activation, but decreased rapidly to 24.3+/-8.3% (M3) and 23.0+/-9.0% (M4) between 21 and 35 sec after activation. Mounib's extender (M3, M4) provided the best cryoprotection to the spermatozoa for all post-thaw sperm quality measurements and at all freezing durations. Sperm motility was positively related to fertility. Our method will make it possible to develop even better extenders and cryoprotectants.

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Year:  2001        PMID: 11245263     DOI: 10.1016/s0093-691x(01)00441-1

Source DB:  PubMed          Journal:  Theriogenology        ISSN: 0093-691X            Impact factor:   2.740


  6 in total

1.  Fish Sperm Assessment Using Software and Cooling Devices.

Authors:  Carina Caldeira; Carles Soler
Journal:  J Vis Exp       Date:  2018-07-28       Impact factor: 1.355

2.  In vitro antioxidant enzyme activity and sperm motility at different temperatures in sterlet Acipenser ruthenus and rainbow trout Oncorhynchus mykiss.

Authors:  Hadiseh Dadras; Viktoriya Dzyuba; Amin Golpour; Miaomiao Xin; Borys Dzyuba
Journal:  Fish Physiol Biochem       Date:  2019-07-08       Impact factor: 2.794

3.  In vivo and in vitro aging of common carp Cyprinus carpio sperm after multiple hormonal application and stripping of males.

Authors:  Songpei Zhang; Yu Cheng; Zuzana Linhartová; Vladimíra Rodinová; Nururshopa Eskander Shazada; Qing Wu; Otomar Linhart
Journal:  Fish Physiol Biochem       Date:  2022-08-17       Impact factor: 3.014

4.  Proteomic characterization of fresh spermatozoa and supernatant after cryopreservation in relation to freezability of carp (Cyprinus carpio L) semen.

Authors:  Mariola A Dietrich; Andrzej Ciereszko
Journal:  PLoS One       Date:  2018-03-22       Impact factor: 3.240

5.  Effects of Cryoprotectants and Diluents on the Cryopreservation of Spermatozoa from Far Eastern Catfish, Silurus asotus.

Authors:  Hyun Woo Gil; Tae Ho Lee; In-Seok Park
Journal:  Dev Reprod       Date:  2017-03-31

6.  Cryobanking of aquatic species.

Authors:  Sonia Martínez-Páramo; Ákos Horváth; Catherine Labbé; Tiantian Zhang; Vanesa Robles; Paz Herráez; Marc Suquet; Serean Adams; Ana Viveiros; Terrence R Tiersch; Elsa Cabrita
Journal:  Aquaculture       Date:  2016-06-01       Impact factor: 4.242

  6 in total

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