Cargando…

Fertility of frozen-thawed stallion semen cannot be predicted by the currently used laboratory methods

The aim of the project was to use current simple and practical laboratory tests and compare results with the foaling rates of mares inseminated with commercially produced frozen semen. In Exp. 1, semen was tested from 27 and in Exp. 2 from 23 stallions; 19 stallions participated in both experiments....

Descripción completa

Detalles Bibliográficos
Autores principales: Kuisma, P, Andersson, M, Koskinen, E, Katila, T
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1564023/
https://www.ncbi.nlm.nih.gov/pubmed/16987393
http://dx.doi.org/10.1186/1751-0147-48-14
_version_ 1782129535690473472
author Kuisma, P
Andersson, M
Koskinen, E
Katila, T
author_facet Kuisma, P
Andersson, M
Koskinen, E
Katila, T
author_sort Kuisma, P
collection PubMed
description The aim of the project was to use current simple and practical laboratory tests and compare results with the foaling rates of mares inseminated with commercially produced frozen semen. In Exp. 1, semen was tested from 27 and in Exp. 2 from 23 stallions; 19 stallions participated in both experiments. The mean number of mares per stallion in both experiments was 37 (min. 7, max. 121). Sperm morphology was assessed and bacterial culture performed once per stallion. In Exp. 1, progressive motility after 0, 1, 2, 3, and 4 h of incubation using light microscopy, motility characteristics measured with an automatic sperm analyzer, plasma membrane integrity using carboxyfluorescein diacetate/propidium iodide (CFDA/PI) staining and light microscopy, plasma membrane integrity using PI staining and a fluorometer, plasma membrane integrity using a resazurin reduction test, and sperm concentration were evaluated. In Exp. 2, the same tests as in Exp. 1 and a hypo-osmotic swelling test (HOST) using both light microscopy and a fluorometer were performed immediately after thawing and after a 3-h incubation. Statistical analysis was done separately to all stallions and to those having ≥ 20 mares; in addition, stallions with foaling rates < 60 or ≥ 60% were compared. In Exp. 1, progressive motility for all stallions after a 2 – 4-h incubation correlated with the foaling rate (correlation coefficients 0.39 – 0.51), (p < 0.05). In stallions with > 20 mares, the artificial insemination dose showed a correlation coefficient of -0.58 (p < 0.05). In Exp. 2, the HOST immediately after thawing showed a negative correlation with foaling rate (p < 0.05). No single test was consistently reliable for predicting the fertilizing capacity of semen, since the 2 experiments yielded conflicting results, although the same stallions sometimes participated in both. This shows the difficulty of frozen semen quality control in commercially produced stallion semen, and on the other hand, the difficulty of conducting fertility trials in horses.
format Text
id pubmed-1564023
institution National Center for Biotechnology Information
language English
publishDate 2006
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-15640232006-09-12 Fertility of frozen-thawed stallion semen cannot be predicted by the currently used laboratory methods Kuisma, P Andersson, M Koskinen, E Katila, T Acta Vet Scand Research The aim of the project was to use current simple and practical laboratory tests and compare results with the foaling rates of mares inseminated with commercially produced frozen semen. In Exp. 1, semen was tested from 27 and in Exp. 2 from 23 stallions; 19 stallions participated in both experiments. The mean number of mares per stallion in both experiments was 37 (min. 7, max. 121). Sperm morphology was assessed and bacterial culture performed once per stallion. In Exp. 1, progressive motility after 0, 1, 2, 3, and 4 h of incubation using light microscopy, motility characteristics measured with an automatic sperm analyzer, plasma membrane integrity using carboxyfluorescein diacetate/propidium iodide (CFDA/PI) staining and light microscopy, plasma membrane integrity using PI staining and a fluorometer, plasma membrane integrity using a resazurin reduction test, and sperm concentration were evaluated. In Exp. 2, the same tests as in Exp. 1 and a hypo-osmotic swelling test (HOST) using both light microscopy and a fluorometer were performed immediately after thawing and after a 3-h incubation. Statistical analysis was done separately to all stallions and to those having ≥ 20 mares; in addition, stallions with foaling rates < 60 or ≥ 60% were compared. In Exp. 1, progressive motility for all stallions after a 2 – 4-h incubation correlated with the foaling rate (correlation coefficients 0.39 – 0.51), (p < 0.05). In stallions with > 20 mares, the artificial insemination dose showed a correlation coefficient of -0.58 (p < 0.05). In Exp. 2, the HOST immediately after thawing showed a negative correlation with foaling rate (p < 0.05). No single test was consistently reliable for predicting the fertilizing capacity of semen, since the 2 experiments yielded conflicting results, although the same stallions sometimes participated in both. This shows the difficulty of frozen semen quality control in commercially produced stallion semen, and on the other hand, the difficulty of conducting fertility trials in horses. BioMed Central 2006-08-17 /pmc/articles/PMC1564023/ /pubmed/16987393 http://dx.doi.org/10.1186/1751-0147-48-14 Text en Copyright © 2006 Kuisma et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Kuisma, P
Andersson, M
Koskinen, E
Katila, T
Fertility of frozen-thawed stallion semen cannot be predicted by the currently used laboratory methods
title Fertility of frozen-thawed stallion semen cannot be predicted by the currently used laboratory methods
title_full Fertility of frozen-thawed stallion semen cannot be predicted by the currently used laboratory methods
title_fullStr Fertility of frozen-thawed stallion semen cannot be predicted by the currently used laboratory methods
title_full_unstemmed Fertility of frozen-thawed stallion semen cannot be predicted by the currently used laboratory methods
title_short Fertility of frozen-thawed stallion semen cannot be predicted by the currently used laboratory methods
title_sort fertility of frozen-thawed stallion semen cannot be predicted by the currently used laboratory methods
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1564023/
https://www.ncbi.nlm.nih.gov/pubmed/16987393
http://dx.doi.org/10.1186/1751-0147-48-14
work_keys_str_mv AT kuismap fertilityoffrozenthawedstallionsemencannotbepredictedbythecurrentlyusedlaboratorymethods
AT anderssonm fertilityoffrozenthawedstallionsemencannotbepredictedbythecurrentlyusedlaboratorymethods
AT koskinene fertilityoffrozenthawedstallionsemencannotbepredictedbythecurrentlyusedlaboratorymethods
AT katilat fertilityoffrozenthawedstallionsemencannotbepredictedbythecurrentlyusedlaboratorymethods