Effects of extender composition, cooling rate and freezing on the fertilisation viability of spermatozoa of the Pacific oyster (Crassostrea gigas)

Abstract The aim of this research was to optimise protocols for freezing spermatozoa of the Pacific oyster. All the phases of the cryopreservation procedure (choice of cryoprotectant, cooling, freezing, and thawing) were studied in relation to the species of spermatozoa to restore on thawing the mor...

Full description

Bibliographic Details
Main Authors: S. IEROPOLI, P. MASULLO, M. DO ESPIRITO SANTO, SANSONE, GIOVANNI
Other Authors: S., Ieropoli, P., Masullo, M., DO ESPIRITO SANTO, Sansone, Giovanni
Format: Article in Journal/Newspaper
Language:English
Published: 2004
Subjects:
Online Access:http://hdl.handle.net/11588/204687
_version_ 1821496441172918272
author S. IEROPOLI
P. MASULLO
M. DO ESPIRITO SANTO
SANSONE, GIOVANNI
author2 S., Ieropoli
P., Masullo
M., DO ESPIRITO SANTO
Sansone, Giovanni
author_facet S. IEROPOLI
P. MASULLO
M. DO ESPIRITO SANTO
SANSONE, GIOVANNI
author_sort S. IEROPOLI
collection IRIS Università degli Studi di Napoli Federico II
description Abstract The aim of this research was to optimise protocols for freezing spermatozoa of the Pacific oyster. All the phases of the cryopreservation procedure (choice of cryoprotectant, cooling, freezing, and thawing) were studied in relation to the species of spermatozoa to restore on thawing the morphological and physiological characteristics of fresh semen. The choice of type and concentration of cryoprotectant in which semen is incubated before freezing is fundamental for a successful cryopreservation: the cryoprotectants (dimethylsulfoxide—Me2SO, ethylene glycol—EG, propylene glycol—PG, and glycerol in concentrations between 5 and 15%) were tested for their toxicity on the semen exposed up to 30 min at +26 _C (room temperature) by evaluating its ability to fertilise and the embryo development to the regular D larval stage. The best cryoprotectants, Me2SO, EG, and PG 5, 10, and 15% respectively, were used for the pre-cooling (adaptation/cooling) tests. Two different adaptation/cooling procedures were tested: (A) from +26 _C to 0–2 _C (2.6 _C/min) and (B) at +26 _C for 15 min. Lastly, using the cryoprotectants and the adaptation procedure (B) that had given the best results in the preceding stages of the experiment, four cooling rates were tested: 6, 11, 16, and 21 _C/min. It was seen that the semen that was incubated with EG 10%, adapted at +26 _C for 15 min, and then cooled at a rate of 6 _C/min showed a percentage of regular D larvae on thawing comparable to that of fresh semen (p > 0.05).
format Article in Journal/Newspaper
genre Crassostrea gigas
Pacific oyster
genre_facet Crassostrea gigas
Pacific oyster
geographic Pacific
geographic_facet Pacific
id ftunivnapoliiris:oai:www.iris.unina.it:11588/204687
institution Open Polar
language English
op_collection_id ftunivnapoliiris
op_relation volume:49
firstpage:250
lastpage:257
journal:CRYOBIOLOGY
http://hdl.handle.net/11588/204687
op_rights info:eu-repo/semantics/closedAccess
publishDate 2004
record_format openpolar
spelling ftunivnapoliiris:oai:www.iris.unina.it:11588/204687 2025-01-16T21:35:28+00:00 Effects of extender composition, cooling rate and freezing on the fertilisation viability of spermatozoa of the Pacific oyster (Crassostrea gigas) S. IEROPOLI P. MASULLO M. DO ESPIRITO SANTO SANSONE, GIOVANNI S., Ieropoli P., Masullo M., DO ESPIRITO SANTO Sansone, Giovanni 2004 STAMPA http://hdl.handle.net/11588/204687 eng eng volume:49 firstpage:250 lastpage:257 journal:CRYOBIOLOGY http://hdl.handle.net/11588/204687 info:eu-repo/semantics/closedAccess Cryopreservation Oyster Crassostrea giga Spermatozoa info:eu-repo/semantics/article 2004 ftunivnapoliiris 2024-06-17T15:19:24Z Abstract The aim of this research was to optimise protocols for freezing spermatozoa of the Pacific oyster. All the phases of the cryopreservation procedure (choice of cryoprotectant, cooling, freezing, and thawing) were studied in relation to the species of spermatozoa to restore on thawing the morphological and physiological characteristics of fresh semen. The choice of type and concentration of cryoprotectant in which semen is incubated before freezing is fundamental for a successful cryopreservation: the cryoprotectants (dimethylsulfoxide—Me2SO, ethylene glycol—EG, propylene glycol—PG, and glycerol in concentrations between 5 and 15%) were tested for their toxicity on the semen exposed up to 30 min at +26 _C (room temperature) by evaluating its ability to fertilise and the embryo development to the regular D larval stage. The best cryoprotectants, Me2SO, EG, and PG 5, 10, and 15% respectively, were used for the pre-cooling (adaptation/cooling) tests. Two different adaptation/cooling procedures were tested: (A) from +26 _C to 0–2 _C (2.6 _C/min) and (B) at +26 _C for 15 min. Lastly, using the cryoprotectants and the adaptation procedure (B) that had given the best results in the preceding stages of the experiment, four cooling rates were tested: 6, 11, 16, and 21 _C/min. It was seen that the semen that was incubated with EG 10%, adapted at +26 _C for 15 min, and then cooled at a rate of 6 _C/min showed a percentage of regular D larvae on thawing comparable to that of fresh semen (p > 0.05). Article in Journal/Newspaper Crassostrea gigas Pacific oyster IRIS Università degli Studi di Napoli Federico II Pacific
spellingShingle Cryopreservation
Oyster
Crassostrea giga
Spermatozoa
S. IEROPOLI
P. MASULLO
M. DO ESPIRITO SANTO
SANSONE, GIOVANNI
Effects of extender composition, cooling rate and freezing on the fertilisation viability of spermatozoa of the Pacific oyster (Crassostrea gigas)
title Effects of extender composition, cooling rate and freezing on the fertilisation viability of spermatozoa of the Pacific oyster (Crassostrea gigas)
title_full Effects of extender composition, cooling rate and freezing on the fertilisation viability of spermatozoa of the Pacific oyster (Crassostrea gigas)
title_fullStr Effects of extender composition, cooling rate and freezing on the fertilisation viability of spermatozoa of the Pacific oyster (Crassostrea gigas)
title_full_unstemmed Effects of extender composition, cooling rate and freezing on the fertilisation viability of spermatozoa of the Pacific oyster (Crassostrea gigas)
title_short Effects of extender composition, cooling rate and freezing on the fertilisation viability of spermatozoa of the Pacific oyster (Crassostrea gigas)
title_sort effects of extender composition, cooling rate and freezing on the fertilisation viability of spermatozoa of the pacific oyster (crassostrea gigas)
topic Cryopreservation
Oyster
Crassostrea giga
Spermatozoa
topic_facet Cryopreservation
Oyster
Crassostrea giga
Spermatozoa
url http://hdl.handle.net/11588/204687