Title of article :
Advances in cryopreservation of stallion semen in modified INRA82
Author/Authors :
O. and Vidament، نويسنده , , M and Yvon، نويسنده , , J.M and Couty، نويسنده , , I and Arnaud، نويسنده , , G and Nguekam-Feugang، نويسنده , , J. de la Noue، نويسنده , , P and Cottron، نويسنده , , S and Le Tellier، نويسنده , , A and Noel، نويسنده , , F and Palmer، نويسنده , , E and Magistrini، نويسنده , , M، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2001
Pages :
18
From page :
201
To page :
218
Abstract :
In the procedure used in this paper, semen was first diluted in INRA82+2% egg yolk (E1) at 37 °C. Before or after cooling to 4 °C, semen was centrifuged and diluted in E1+2.5% glycerol (E2). Cooled semen was frozen in 0.5-ml straws. Straws were thawed at 37 °C for 30 s. For fertility trials, frozen ejaculates were used only if total post-thaw motility was above 35%. Most mares were inseminated two times before ovulation with 400×106 total spermatozoa every 24 h. This paper presents post-thaw motility (CASA) and fertility results obtained when some steps of the procedure were evaluated. the first three jets of ejaculate before the centrifugation did not improve post-thaw motility compared to use of the whole semen (25% versus 25%, 2 stallions×12 ejaculates, P>0.80). When the first dilution was performed in E2 at 22 °C instead of in E1 at 37 °C, motility was slightly improved (38% versus 36%, n>283 ejaculates per group, P<0.04) but fertility was similar (51% versus 58%, n>196 cycles per group, P>0.10). Coating the spermatozoa with 0.5, 1, 2, 4 and 8 mM of Concanavalin A resulted in unchanged post-thaw motility (6 stallions×3 ejaculates, P>0.05). The extender E2 was modified or supplemented with different substances. Increasing egg yolk concentration from 2 to 4% (v/v) did not increase post-thaw motility (42% versus 34%, 6 stallions×2 ejaculates, P>0.05). Different glycerol concentrations (range: 1.7–3.7%) had no significant effect on post-thaw motility even though 2.4–2.8% resulted in a nonsignificant higher motility (7 stallions×2 ejaculates, P>0.05). Glutamine at 50 mM in E2 improved post-thaw motility compared with no glutamine (49% versus 46%, n>584 ejaculates per group, P<0.0001) but not fertility (53% versus 54%, n>451 cycles per group, P>0.80). Thawing at 75 °C for 10 s slightly increased motility after 120 min at 37 °C (6 stallions×1 ejaculate, P<0.05) but no effect on per-cycle fertility was noted (32% (19 cycles) versus 41% (17 cycles), P>0.50). When post-thaw dilution was performed using a fixed molarity multi-step system (25 mOsm per step) from various osmolarities (900–690 mOsm) to 365 mOsm, motility was unaffected compared with dilution in one step (36% versus 38%, 6 stallions×1 ejaculate, P>0.20).
Keywords :
stallion , Spermatozoa , Cryopreservation , Glycerol , Glutamine , Osmotic injury , thawing
Journal title :
Animal Reproduction Science
Serial Year :
2001
Journal title :
Animal Reproduction Science
Record number :
1907132
Link To Document :
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