Title of article :
Gene banking of the neotropical fish Leporinus obtusidens (Valenciennes, 1836): A protocol to freeze its sperm in the field
Author/Authors :
Taitson، نويسنده , , P.F. and Chami، نويسنده , , Cristina E. and Godinho، نويسنده , , H.P.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Pages :
9
From page :
283
To page :
291
Abstract :
A practical sperm cryopreservation protocol using a dry-shipper and a diluent of simple composition is described for the neotropical fish Leporinus obtusidens (Valenciennes, 1836). The cooling rate of the dry-shipper and its period of useful time, established under laboratory conditions, were respectively 25.7–30.8 °C/min (between 0 and −60 °C) and 9 days after charging. Sperm donors were selected on the basis of their hyperemic genital papilla and the ability to ooze milt under gentle manual pressure, during the reproductive months of November to January. Milt volume (1.3 ± 0.3 mL; n = 9 fish), fresh sperm motility rate (93.3 ± 2.5%; n = 6 fish), and sperm concentration (10.9 ± 3.0 × 109 spermatozoa/mL of milt) were obtained. The sperm cryopreservation experiments were conducted with the following cryoprotectants (all at 10%, before mixing with milt): dimethyl sulphoxide (DMSO; n = 10 fish), methanol (n = 6 fish), propanediol (n = 6 fish) and ethylene glycol (n = 5 fish). Glucose (5%) and henʹs egg yolk (10%) made up the diluents containing DMSO, ethylene glycol or propanediol. Milk powder (10%) replaced henʹs egg yolk in the diluent containing methanol. Distilled water (up to 100%) completed the diluent solutions. Milt freezing (in 0.5-mL straws) was performed in the dry-shipper after 1:5 (milt:diluent) dilution. Thawed sperm cryopreserved in DMSO-containing diluent and activated by 119 mM NaHCO3 gave the highest motility rate (62 ± 14%). The fertilizing capacity of L. obtusidens sperm was tested using the combination of DMSO-containing diluent as the cryoprotectant and 119 mM NaHCO3 as the activating solution. Oocytes were obtained from artificial spawning and fertilized with different proportions of spermatozoa. The greatest rate of fertilization (74%) occurred when the ratio of about 112,000 motile spermatozoa:oocyte was used. Thus, a protocol to freeze L. obtusidens sperm can be elaborated as follows. Milt (<1.5 mL fish−1) was readily available only in November to January; a simple solution, composed of 10% DMSO (concentration before adding milt), 5% glucose, and 10% hen yolk egg, in distilled water, was used as sperm diluent; cooling rate of 25–30 °C/min, yielded in a portable dry-shipper, was adequate to freeze diluted milt (1:5; milt:diluent), in 5-mL straws; about 112,000 thawed motile spermatozoa:oocyte activated by 119 mM NaHCO3 assured a fertilization rate of 74%.
Keywords :
Leporinus obtusidens , Sperm cryopreservation , Neotropical fish , Fish gene banking
Journal title :
Animal Reproduction Science
Serial Year :
2008
Journal title :
Animal Reproduction Science
Record number :
1909986
Link To Document :
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