Cryopreservation of boar semen. II: Effect of cooling rate and duration of freezing point plateau on boar semen frozen in mini- and maxi-straws and plastic bags
- PMID: 1818504
- PMCID: PMC8127895
- DOI: 10.1186/BF03546945
Cryopreservation of boar semen. II: Effect of cooling rate and duration of freezing point plateau on boar semen frozen in mini- and maxi-straws and plastic bags
Abstract
The post-thaw motility and the acrosome integrity of semen from 4 boars frozen with a programmable freezing machine, in mini (0.25 ml) and maxi (5 ml) plastic straws and in 10 x 5 cm Teflon FEP-plastic bags (0.12 mm thick, 5 ml), were compared. The freezing of the semen was monitored by way of thermo-couples placed in the straws and the bags. Three freezing programmes were used, namely A: from +5 degrees C, at a rate of 3 degrees C/min, to -6 degrees C, held for 1 min at -6 degrees C, and followed by a cooling rate of 20 degrees C/min to -100 degrees C; B: a similar curve except that there was no holding time at -6 degrees C and that the cooling rate was 30 degrees C/min, and C: from +5 degrees C to -100 degrees C, with a cooling rate of 35 degrees C/min, followed by storage in liquid N2. Despite the freezing curve assayed, both the mini-straws and the bags depicted much shorter freezing point plateaus as compared to the maxi-straws. Post-thaw sperm motility as well as the amount of normal apical ridges were equally significantly higher when semen was frozen in mini-straws or in bags than in maxi-straws. Significant differences in these post-thawing parameters were obtained between the freezing curves used. The stepwise freezing procedure A appeared as the best alternative for boar semen, considering this in vitro evaluation.
Spermiemotilitet och akrosommorfologi efter djupfrysning-upptining undersöktes hos spermier från fyra gaitar som frysts med hjälp av en programmerbar frysmaskin i ministrån (0,25 ml), maxistrån (5 ml) och plastpåsar (5ml, 10 × 5 cm) tilverkade av 0,12 mm tjock Teflon FEP-film. Frysningsförloppet studerades med hjälp av “termocouples”, som placerais i strån och plastpåsar. Följande 3 frysprogram användes: A- från 5° C till −6° C med 3° C/min, uppehåll under en minut vid −6°C, från −6°C till −100° C med 20° C/min; B− likartad frysningsförlopp, men inget uppehåll vid −6°C och 30° C/min från −6°C till -100° C; C-från 5°C till −100° C med 35° C/min, åtföljt av nedsänkning i flytande kväve. Trots fryskurvans utseende, hade båda ministrån och påsar kortare fryspunktplatåer än maxistrån. Såväl upptiningsmotiliteten som akrosommorfologin var signifikant bättre hos spermier som frysts i ministrån och plastpåsar jämfört med maxistrån. Signifikanta skillnader påvisades ocksá mellan de 3 frysprogrammen. Frysprogram A lämpade sig bäst för galtspermier att döma av resultaten från in vitro testerna efter djupfrysningupptining.
Similar articles
-
Cryopreservation of boar semen in mini- and maxi-straws.Zentralbl Veterinarmed A. 1990 Oct;37(9):651-8. doi: 10.1111/j.1439-0442.1990.tb00958.x. Zentralbl Veterinarmed A. 1990. PMID: 2127970
-
Cryo-scanning electron microscopy discloses differences in dehydration of frozen boar semen stored in large containers.Reprod Domest Anim. 2009 Feb;44(1):62-8. doi: 10.1111/j.1439-0531.2007.00994.x. Epub 2008 Jul 28. Reprod Domest Anim. 2009. PMID: 18673328
-
In vivo fertilizing capacity of deep frozen boar semen packaged in plastic bags and maxi-straws.Zentralbl Veterinarmed A. 1991 May;38(4):281-6. doi: 10.1111/j.1439-0442.1991.tb01014.x. Zentralbl Veterinarmed A. 1991. PMID: 1907787
-
Cryopreservation of boar semen: equilibrium freezing in the cryomicroscope and in straws.Theriogenology. 2005 Jan 15;63(2):383-95. doi: 10.1016/j.theriogenology.2004.09.019. Theriogenology. 2005. PMID: 15626406 Review.
-
Fundamentals and recent development in cryopreservation of bull and boar semen.Vet Q. 1997 Sep;19(3):135-8. doi: 10.1080/01652176.1997.9694758. Vet Q. 1997. PMID: 9323856 Review.
Cited by
-
Effect of n-3 fatty acids and α-tocopherol on post-thaw parameters and fatty acid composition of bovine sperm.J Assist Reprod Genet. 2012 Oct;29(10):1051-6. doi: 10.1007/s10815-012-9834-7. Epub 2012 Aug 7. J Assist Reprod Genet. 2012. PMID: 22869241 Free PMC article.
-
Revisiting the Injury Mechanism of Goat Sperm Caused by the Cryopreservation Process from a Perspective of Sperm Metabolite Profiles.Int J Mol Sci. 2024 Aug 22;25(16):9112. doi: 10.3390/ijms25169112. Int J Mol Sci. 2024. PMID: 39201798 Free PMC article.
-
Cryopreservation of boar semen. III: Ultrastructure of boar spermatozoa frozen ultra-rapidly at various stages of conventional freezing and thawing.Acta Vet Scand. 1991;32(4):463-71. doi: 10.1186/BF03546946. Acta Vet Scand. 1991. PMID: 1818505 Free PMC article.
References
-
- Bwanga CO, Einarsson S, Rodriguez-Martinez H. Deep freezing of boar semen in plastic bags and straws. Reprod. Dom. Anim. 1991;26:117–125. doi: 10.1111/j.1439-0531.1991.tb01528.x. - DOI
-
- Courtens JL, Paquignon M: Ultrastructure of fresh, frozen and frozen-thawed spermatozoa of the boar. In: Johnson LA, Larsson K (Eds.): Deep Freezing of Boar Semen. Swedish Univ. of Agric. Sci., Uppsala 1985, 61–87.
-
- de Leeuw FE, Colenbrander B, Verkleij AJ: Cooling and freezing injury to the plasma membrane of boar spermatozoa. Proc. 2nd Int. Conf. Boar Semen Preserv., Beltsville 1990 A7: 27.
-
- Einarsson S: Studies on the composition of epididymal content and semen in the boar. Acta vet. scand. 1971, Suppl. 36. - PubMed
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources