- II — Technologies de Conservation des Ressources Génétiques Animales et Végétales / Technologies of Conservation for Animal and Plant Genetic Resources
- Open access
- Published:
Cholesterol/phospholipid ratio in sperm of several domestic species does not directly predict sperm fitness for cryopreservation
Le rapport cholestérol/phospholipide dans le sperme de diverses espèces domestiques n’est pas un indicateur direct de l’aptitude à la congélation du sperme
Genetics Selection Evolution volume 33, Article number: S61 (2001)
Abstract
Sperm cryopreservation is used for preservation and diffusion of genetic diversity and genetic progress. One approach to improve cryopreservation is to identify and control the cellular parameters responsible for intrinsic sperm fitness for cryopreservation. The aim of this study was to determine if a relationship exists between sperm cholesterol/phospholipid molar ratio (CHO/PL) and sperm fitness for cryopreservation. CHO/PL in goat and boar semen were respectively 0.281 ± 0.048 (n = 112) and 0.375 ± 0.043 (n = 47). CHO/PL of washed stallion spermatozoa was 0.541 ± 0.072 (n = 17). In stallion spermatozoa and goat semen, CHO/PL and sperm motility after thawing were negatively correlated, although the significance of this relation fluctuated between ejaculates (stallion) and between months of collection (goat). In boar, mobility parameters after thawing were not related to CHO/PL, but a positive correlation was noted between CHO/PL and the percentage of spermatozoa alive and normal 120 min after thawing. No relationship was found between blood plasma cholesterol (goat: 1160 nmol.mL−1 ± 186; boar: 1410 nmol.mL−1 ± 200) or seminal plasma cholesterol (boar sperm rich fraction: 104 nmol.mL−1 ±52) and sperm CHO/PL. To conclude, sperm CHO/PL is not a direct indicator of sperm fitness for cryopreservation. However, as supported by the observed correlation, it could not be ruled out that CHO/PL is involved in the cryopreservation success.
Résumé
La congélation du sperme est utilisée pour la conservation et la diffusion de la diversité et du progrès génétique. Une approche permettant d’améliorer la qualité du sperme congelé est d’identifier et de contrôler les paramètres cellulaires impliqués dans l’aptitude intrinsèque du sperme à la congélation. Le but de la présente étude était de déterminer si une relation existait entre le rapport molaire cholestérol/phospholipide (CHO/PL) du sperme et son aptitude à la congélation. Le rapport CHO/PL de la semence de bouc et de verrat était de 0.281±0.048 (n = 112) et 0.375±0.043 (n = 47) respectivement. Le rapport CHO/PL des spermatozoïdes lavés d’étalon était 0.541 ±0.072 (n = 17). Pour les spermatozoïdes d’étalon et la semence de bouc, une corrélation négative a été trouvée entre ce rapport et les paramètres de mobilité des spermatozoïdes après décongélation bien que la signification statistique de cette relation soit fluctuante entre éjaculats (étalon) et entre les mois de collecte (bouc). Chez le verrat, les paramètres de mobilité après décongélation n’ont pu être corrélés au rapport CHO/PL, mais une corrélation positive est apparue entre le rapport CHO/PL et le pourcentage de spermatozoïdes vivants normaux 120 min après la décongélation. Aucune relation n’a été trouvée entre le cholestérol du plasma sanguin (bouc: 1160 nmol.mL−1 ± 186; verrat: 1410 nmol.mL−1 ± 200) ou du plasma séminal de la fraction riche de la semence (verrat: 104 nmol.mL−1 ± 52) et le rapport CHO/PL. En conclusion, le rapport CHO/PL n’est pas un indicateur direct de l’aptitude d’une semence à la congélation. Cependant, les corrélations observées ne permettent pas d’exclure que le rapport CHO/PL est impliqué dans le succès de la congélation.
References
Ansah G.A., Buckland R.B., Genetic variation in fowl semen cholesterol and phospholipid levels and the relationship of these lipids with fertility of frozen-thawed and fresh semen, Poult. Sci. 61 (1982) 623–637.
Arienti G., Carlini E., De Cosmo A.M., Di Profio P., Palmerini C.A., Prostasome-like particles in stallion semen, Biol. Reprod. 59 (1998) 309–13.
Bishop M.N.H., Campbell R.C., Hanckock J.L., Semen characteristics and fertility in the bull, J. Agri. Sci. 44 (1954) 227.
Bligh E.G., Dyer W.J., A rapid method of total lipid extraction and purification, Can. J. Biochem. Physiol. 37 (1959) 911–917.
Cerolini S, Maldjian A., Gliozzi T., Pizzi F., Surai P., Noble R., Relationship between lipid composition and viability of boar spermatozoa after freezing/thawing, IV International Conference on Boar Semen Preservation, Beltsville, Maryland, USA 8–11 August 1999.
Corteel J.M., Viabilité des spermatozoides de bouc conservés congelés avec ou sans leur plasma seminal, effet du glucose, Ann. Biol. Bioch. Biophys. 14 (1974) 741–745.
Drobnis E.Z., Crowe L.M., Berger T., Anchordoguy T.J., Overstreet J.W., Crowe J.H., Cold shock damage is due to lipid phase transitions in cell membranes: a demonstration using sperm as a model, J. Exp. Zool. 265 (1993) 432–437.
Goffaux M., L’examen approfondi des anomalies de la semence de taureau, Elev. Insem. 244 (1991) 3–14.
Hammerstedt R.H., Graham E.F., Nolan J.P., Cryopreservation of mammalian sperm: What we ask them to survive, J. Androl. 11 (1990) 73–88.
Iborra A., Companyo M., Martinez P., Morros A., Cholesterol efflux promotes acrosome reaction in goat spermatozoa, Biol. Reprod. 62 (2000) 378–383.
Komarek R.J., Pickett B.W., Gibson E.W., Jensen R.G., Lipids of porcine spermatozoa, seminal plasma and gel, J. Reprod. Fertil. 9 (1965) 131–136.
Labbe C, Maisse G., Influence of rainbow trout thermal acclimation on sperm cryopreservation: Relation to change in the lipid composition of the plasma membrane, Aquaculture 145 (1996) 281–294.
Parks J.E., Hammerstedt R.H., Developmental changes occurring in the lipids of ram epididymal spermatozoa plasma membrane, Biol. Reprod. 32 (1985) 653–668.
Parks J.E., Lynch D.V., Lipid composition and thermotropic phase behavior of boar, bull, stallion, and rooster sperm membranes, Cryobiology 29 (1992) 255–266.
Pursel V.G., Johnson L.A., Freezing of boar spermatozoa: Fertilizing capacity with concentrated semen and a new thawing procedure, J. Anim. Sci. 40 (1975) 99–102.
Quinn P.J., A lipid-phase separation model of low-temperature damage to biological membranes, Cryobiology 22 (1985) 128–146.
Quinn P.J., White I.G., Phospholipid and cholesterol content of epididymal and ejaculated ram spermatozoa and seminal plasma in relation to cold shock, Aust. J. Biol. Sci. 20 (1967) 1205–1215.
Rana A.P., Majumder G.C., Misra S., Ghosh A., Lipid changes of goat sperm plasma membrane during epididymal maturation, Biochim. Biophys. Acta 1061 (1991) 185–196.
Rouser B., Siakotos A., Fleischer S., Quantitative analysis of phospholipids by thin layer chromatography and phosphorus analysis spots, Lipids 1 (1966) 85–86.
Vidament M., Bourgeois C., Noue P., Magistrini M., Centrifugation and addition of glycerol at 22 °C improve frozen stallion semen motility and fertility, Cryobiology 35 (1997) 354.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
About this article
Cite this article
Labbé, C., Bussière, JF., Guillouet, P. et al. Cholesterol/phospholipid ratio in sperm of several domestic species does not directly predict sperm fitness for cryopreservation. Genet Sel Evol 33 (Suppl 1), S61 (2001). https://doi.org/10.1186/BF03500873
Published:
DOI: https://doi.org/10.1186/BF03500873