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Egg yolk plasma can replace egg yolk in stallion freezing extenders
Authors:E Pillet  G DuchampF Batellier  V BeaumalM Anton  S DeshercesE Schmitt  M Magistrini
Institution:a INRA, UMR85 Physiologie de la Reproduction et des Comportements, F-37380 Nouzilly, France; CNRS, F-37380 Nouzilly, France; Université de Tours, F-37041 Tours, France; Haras Nationaux, F-37380 Nouzilly, France
b INRA, UE992 Unité pluri-espèces d'expérimentation animale en physiologie de la reproduction et des comportements, F-37380 Nouzilly, France
c Institut Français du Cheval et de l'Equitation, Haras National de Blois, 69 Avenue Maunoury, BP 14309, F-41043 Blois Cedex, France
d INRA UR 1628 BIA, Interfaces and Dispersed Systems Team, BP 71627, F-44316 Nantes, France
e IMV-Technologies, Department Research and Development, 61302 L'Aigle, France
Abstract:Hen egg yolk is normally used as a cryoprotective agent in semen freezing extenders, but its use has sanitary and practical disadvantages. Moreover the protection afforded by egg yolk has not yet been completely elucidated. The objective of this study was to compare the egg yolk plasma fraction to whole egg yolk in stallion freezing extender. Plasma contains mainly Low Density Lipoproteins (LDL), which are widely presumed to be the cryoprotective agent in egg yolk. Plasma can be produced on an industrial scale, sterilised by gamma-irradiation and incorporated in a ready-to-use extender (our ultimate objective). Plasma samples were subjected to different doses of gamma-irradiation (3, 5, 10 kGy) without dramatic chemical changes that may affect their cryoprotective properties. Stallion semen was frozen with whole egg yolk as a control and with sterilised egg yolk plasma. A fertility trial was conducted on a total of 70 mares' cycles. Fertility per cycle was 60% after insemination of semen frozen in our control extender containing egg yolk (EY), compared to 69% for the extender containing sterilised egg yolk plasma (EYP) (P > 0.05). Post-thaw motility and membrane integrity of spermatozoa were also analysed. Motility parameters were not significantly different between extenders except for the variable VAP (for EY versus EYP, VAP: 63 μm.s−1 versus 59 μm.s−1, a, b: P < 0.001; PROG: 41% versus 39%, RAP30: 56% versus 54%; RAP40: 51% versus 48%, P > 0.05). Membrane integrity was better preserved in EY than in EYP but the difference between extenders was small (P < 0.05). Our results demonstrated that sterilised egg yolk plasma has the potential to replace egg yolk in stallion freezing extender. This experiment led to the development of a ready-to-use extender called INRA-Freeze® (IMV-Technologies, France).
Keywords:Egg yolk plasma  LDL  Cryopreservation  Spermatozoa  Equine
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