Proceedings of the 5th International Symposium on EQUINE ...
Proceedings of the 5th International Symposium on EQUINE ...
Proceedings of the 5th International Symposium on EQUINE ...
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Havemeyer Foundati<strong>on</strong> M<strong>on</strong>ograph Series No. 3Experiment 3: The effect <str<strong>on</strong>g>of</str<strong>on</strong>g> temperature <strong>on</strong>cumulus morphologyCumulus oocyte complexes were recovered fromfollicles within 2 h <str<strong>on</strong>g>of</str<strong>on</strong>g> exteriorisati<strong>on</strong>. The follicleshad been stored at 20–30ºC (n=34) and 35–37ºC(n=40).Experiment 4: The effect <str<strong>on</strong>g>of</str<strong>on</strong>g> time <strong>on</strong> cumulusmorphologyCumulus oocyte complexes (n=298) were left infollicles kept at 35–37ºC for varying lengths <str<strong>on</strong>g>of</str<strong>on</strong>g>time ranging from 0–1, 1–2, 2–3, 3–4, 4–6, 6–8and 8–10 h.STATISTICALANALYSISThe effects <str<strong>on</strong>g>of</str<strong>on</strong>g> temperature and time <strong>on</strong> oocytechromatin c<strong>on</strong>figurati<strong>on</strong> and cumulus morphologywere analysed by a Chi-square test or a Fisher testin case <str<strong>on</strong>g>of</str<strong>on</strong>g> small sample numbers. The nullhypo<str<strong>on</strong>g>the</str<strong>on</strong>g>sis <str<strong>on</strong>g>of</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> statistical test assumed that <str<strong>on</strong>g>the</str<strong>on</strong>g>rewas no difference. A P-value <str<strong>on</strong>g>of</str<strong>on</strong>g> 0.05 or less wasc<strong>on</strong>sidered significant.RESULTSExperiment 1: The effect <str<strong>on</strong>g>of</str<strong>on</strong>g> temperature <strong>on</strong>chromatin c<strong>on</strong>figurati<strong>on</strong>Storing ovaries at ei<str<strong>on</strong>g>the</str<strong>on</strong>g>r 20–30ºC or 35–37ºC didnot affect (P>0.05) chromatin c<strong>on</strong>figurati<strong>on</strong> inoocytes that were fixed within 3 h <str<strong>on</strong>g>of</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> ovaryleaving <str<strong>on</strong>g>the</str<strong>on</strong>g> animal. In <str<strong>on</strong>g>the</str<strong>on</strong>g> 20–30ºC group, 64.3%<str<strong>on</strong>g>of</str<strong>on</strong>g> oocytes were LCC and 35.7% were CC,whereas in <str<strong>on</strong>g>the</str<strong>on</strong>g> 35–37ºC group, 1.7% were FN,78% were LCC and 20.3% were CC.Experiment 2: The effect <str<strong>on</strong>g>of</str<strong>on</strong>g> time <strong>on</strong> chromatinc<strong>on</strong>figurati<strong>on</strong>There was no difference (P>0.1) in oocytechromatin c<strong>on</strong>figurati<strong>on</strong> within <str<strong>on</strong>g>the</str<strong>on</strong>g> first 6 h <str<strong>on</strong>g>of</str<strong>on</strong>g>storage in <str<strong>on</strong>g>the</str<strong>on</strong>g> follicle. The c<strong>on</strong>figurati<strong>on</strong>s startedto change from 4 h <strong>on</strong>wards, but were notsignificantly affected until after 6 h. There was adifference in distributi<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> chromatinc<strong>on</strong>figurati<strong>on</strong>s between 0–6 and 6–12 h (P 0.1). The major changes between 0–6 h and6–12 h were detected in <str<strong>on</strong>g>the</str<strong>on</strong>g> FN c<strong>on</strong>figurati<strong>on</strong> (P