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Reproduction in Domestic Animals - Facultad de Ciencias Veterinarias

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16 t h International Congress on Animal <strong>Reproduction</strong><br />

104 Poster Abstracts<br />

area and disturbed uter<strong>in</strong>e hemodynamics at the mesometrial<br />

attachment.<br />

P229<br />

Effect of prote<strong>in</strong> source <strong>in</strong> stallion semen diluent on the<br />

motility, acrosome <strong>in</strong>tegrity and morphology of sperm<br />

Gibb, Z 1 *, Morris, L 2 , Grupen, C 1 , Evans, G 1 , Maxwell, C 1<br />

1Faculty of Veter<strong>in</strong>ary Science, The University of Sydney, Sydney, Australia;<br />

2EquiBreed Ltd., Cambridge, New Zealand<br />

Introduction Most stallion semen diluents utilise skim milk to<br />

provi<strong>de</strong> protective prote<strong>in</strong>s for sperm. However, milk based diluents<br />

impe<strong>de</strong> sperm motility assessments and reduce the effectiveness of<br />

sta<strong>in</strong><strong>in</strong>g procedures used to process sperm for flow cytometric sort<strong>in</strong>g.<br />

In addition, the variable prote<strong>in</strong> levels and the presence of<br />

uni<strong>de</strong>ntified toxic products <strong>in</strong> milk may vary results. Therefore, a<br />

more precisely <strong>de</strong>f<strong>in</strong>ed diluent prote<strong>in</strong> composition is nee<strong>de</strong>d. The<br />

aim of this study was to ascerta<strong>in</strong> the optimal source of prote<strong>in</strong> <strong>in</strong> a<br />

traditional stallion semen diluent, Kenney’s Modified Tyro<strong>de</strong>’s 1<br />

(KMT) Medium, for handl<strong>in</strong>g and process<strong>in</strong>g stallion sperm prior to<br />

flow cytometric sex-sort<strong>in</strong>g.<br />

Methods and Materials Two ejaculates were collected from each of<br />

three Standardbred stallions. Each ejaculate was diluted <strong>in</strong> traditional<br />

KMT that conta<strong>in</strong>ed skim milk or KMT without skim milk and<br />

supplemented with 0.25mg per ml of either bov<strong>in</strong>e serum album<strong>in</strong><br />

(BSA), β-lactoglobul<strong>in</strong>, glyc<strong>in</strong>e or fetal bov<strong>in</strong>e serum (FBS). Diluted<br />

semen samples were <strong>in</strong>cubated at 34ºC or 5ºC. Subjective motility,<br />

acrosome <strong>in</strong>tegrity and morphology were assessed over a 24 h period.<br />

Results and Discussion After <strong>in</strong>cubation for 3 h at 34ºC, there was no<br />

significant difference between the diluents for total motility,<br />

progressive motility or acrosome status of spermatozoa. After<br />

<strong>in</strong>cubation for 24 h at 34ºC <strong>in</strong> KMT, there was a lower <strong>in</strong>ci<strong>de</strong>nce of<br />

sperm tail abnormalities compared with the other diluents (9.3 vs.<br />

23.2 – 24.5 %; p

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