Survival of several species, along with preservation of the genetic pool is only viable if we can guarantee its conservation throughout time. Canine semen cryopreservation consists on chilling and freezing techniques. Dog semen possesses certain resilience to chilling procedures, which cannot assure long-term gamete preservation. Freezing methods induce a decrease of quality. To overcome this, several extenders to protect spermatozoa have been studied and methods were developed to evaluate both quality and induced damage to the sperm cell by cryopreservation. Yet, it is still difficult to differentiate objectively “good” from “bad” freezers, when both were selected from start as adequate for freezing. In daily practice setting thresholds is often challenging, especially when defining the minimum values to accept semen for freezing. The main objective of this work was to study cold treatment induced alterations in the sperm cell, using conventional semen analysis, along with computerized analysis. A molecular protein study was also conducted, once molecular markers may provide an increase value in the study of the intrinsic mechanisms of canine sperm sensitivity to cryopreservation.
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Survival of several species, along with preservation of the genetic pool is only viable if we can guarantee its conservation throughout time. Canine semen cryopreservation consists on chilling and freezing techniques. Dog semen possesses certain resilience to chilling procedures, which cannot assure long-term gamete preservation. Freezing methods induce a decrease of quality. To overcome this, several extenders to protect spermatozoa have been studied and methods were developed to evaluate both quality and induced damage to the sperm cell by cryopreservation. Yet, it is still difficult to differentiate objectively “good” from “bad” freezers, when both were selected from start as adequate for freezing. In daily practice setting thresholds is often challenging, especially when defining the minimum values to accept semen for freezing. The main objective of this work was to study cold treatment induced alterations in the sperm cell, using conventional semen analysis, along with computerized analysis. A molecular protein study was also conducted, once molecular markers may provide an increase value in the study of the intrinsic mechanisms of canine sperm sensitivity to cryopreservation.
Paulo Alexandre Paulos Borges, graduated in the University of Trás-os-Montes e Alto Douro (UTAD), Vila Real, Portugal. ECAR Resident and actual consultant at CERCA (Centre d’Etudes en Reproduction des Carnivores) at the National Veterinary School of Maisons-Alfort (ENVA), Paris, France.
Les informations fournies dans la section « A propos du livre » peuvent faire référence à une autre édition de ce titre.
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Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Survival of several species, along with preservation of the genetic pool is only viable if we can guarantee its conservation throughout time. Canine semen cryopreservation consists on chilling and freezing techniques. Dog semen possesses certain resilience to chilling procedures, which cannot assure long-term gamete preservation. Freezing methods induce a decrease of quality. To overcome this, several extenders to protect spermatozoa have been studied and methods were developed to evaluate both quality and induced damage to the sperm cell by cryopreservation. Yet, it is still difficult to differentiate objectively 'good' from 'bad' freezers, when both were selected from start as adequate for freezing. In daily practice setting thresholds is often challenging, especially when defining the minimum values to accept semen for freezing. The main objective of this work was to study cold treatment induced alterations in the sperm cell, using conventional semen analysis, along with computerized analysis. A molecular protein study was also conducted, once molecular markers may provide an increase value in the study of the intrinsic mechanisms of canine sperm sensitivity to cryopreservation. N° de réf. du vendeur 9783659624735
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Taschenbuch. Etat : Neu. This item is printed on demand - Print on Demand Titel. Neuware -Survival of several species, along with preservation of the genetic pool is only viable if we can guarantee its conservation throughout time. Canine semen cryopreservation consists on chilling and freezing techniques. Dog semen possesses certain resilience to chilling procedures, which cannot assure long-term gamete preservation. Freezing methods induce a decrease of quality. To overcome this, several extenders to protect spermatozoa have been studied and methods were developed to evaluate both quality and induced damage to the sperm cell by cryopreservation. Yet, it is still difficult to differentiate objectively 'good' from 'bad' freezers, when both were selected from start as adequate for freezing. In daily practice setting thresholds is often challenging, especially when defining the minimum values to accept semen for freezing. The main objective of this work was to study cold treatment induced alterations in the sperm cell, using conventional semen analysis, along with computerized analysis. A molecular protein study was also conducted, once molecular markers may provide an increase value in the study of the intrinsic mechanisms of canine sperm sensitivity to cryopreservation.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 80 pp. Englisch. N° de réf. du vendeur 9783659624735
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Taschenbuch. Etat : Neu. Comparison of canine sperm quality under different temperature storage | Paulo Borges (u. a.) | Taschenbuch | 80 S. | Englisch | 2014 | LAP LAMBERT Academic Publishing | EAN 9783659624735 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu. N° de réf. du vendeur 104995896
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