Literature DB >> 23427145

The specific response to capacitating stimuli is a sensitive indicator of chilling injury in hypothermically stored boar spermatozoa.

S Schmid1, H Henning, H Oldenhof, W F Wolkers, A M Petrunkina, D Waberski.   

Abstract

Boar spermatozoa are sensitive to storage temperatures below 15 °C. Chilling injury causes loss of motility and membrane integrity in a minority of cells, whereas the main population displays sublethal changes compromising fertility. In this study, changes of the response to capacitation conditions in hypothermically stored boar spermatozoa have been examined using a kinetic approach with well-defined test and control media. Ejaculates of seven boars were diluted in Beltsville Thawing Solution kept for 3 h at 22 °C or cooled to 17, 10 and 5 °C and stored for 24 and 96 h. At each time point, the standard sperm parameters motility and membrane integrity were evaluated. Subsequently, washed subsamples were incubated in capacitating and control medium before flow cytometric analysis of intracellular calcium content using the Fluo-3 probe and changes in phospholipid disorder using merocyanine. Kinetic changes of response parameters were monitored in viable (plasma membrane intact) cells. Chilling led to a loss of standard sperm quality traits in a minor subpopulation of cells, whereas storage length had no effect on these parameters. However, responses to incubation as determined by the loss of live cells with low intracellular calcium content showed marked changes in relation to storage conditions. The specific responsiveness to capacitation conditions decreased in close relation to storage temperature and length. In contrast, the merocyanine probe revealed to be limited to detect effects of hypothermic storage. Using Fourier transform infrared spectroscopy, no influence of chilling on membrane phase behaviour was found that might implicate decreased sperm function. In conclusion, assessment of response to capacitating media by monitoring intracellular calcium levels provides a sensitive measure for chilling injury in extended boar semen, and therefore, deserves implementation in hypothermic storage tests.
© 2013 American Society of Andrology and European Academy of Andrology.

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Year:  2013        PMID: 23427145     DOI: 10.1111/j.2047-2927.2013.00045.x

Source DB:  PubMed          Journal:  Andrology        ISSN: 2047-2919            Impact factor:   3.842


  8 in total

1.  Bisphenol A Diglycidyl Ether (BADGE) and Progesterone Do Not Induce Ca2+ Signals in Boar Sperm Cells.

Authors:  Anders Rehfeld; Noelia Mendoza; Raquel Ausejo; Niels Erik Skakkebæk
Journal:  Front Physiol       Date:  2020-07-07       Impact factor: 4.566

2.  Sperm function in vitro and fertility after antibiotic-free, hypothermic storage of liquid preserved boar semen.

Authors:  Dagmar Waberski; Anne-Marie Luther; Benita Grünther; Helen Jäkel; Heiko Henning; Charlotte Vogel; Wolfgang Peralta; Karl Fritz Weitze
Journal:  Sci Rep       Date:  2019-10-14       Impact factor: 4.379

3.  Fluorescent analysis of boar sperm capacitation process in vitro.

Authors:  Lukas Ded; Pavla Dostalova; Eva Zatecka; Andrej Dorosh; Katerina Komrskova; Jana Peknicova
Journal:  Reprod Biol Endocrinol       Date:  2019-12-19       Impact factor: 5.211

4.  Temperature limits for storage of extended boar semen from the perspective of the sperm's energy status.

Authors:  Heiko Henning; Quynh Thu Nguyen; Ulrike Wallner; Dagmar Waberski
Journal:  Front Vet Sci       Date:  2022-08-05

5.  Energy metabolic state in hypothermically stored boar spermatozoa using a revised protocol for efficient ATP extraction.

Authors:  Quynh Thu Nguyen; Ulrike Wallner; Marion Schmicke; Dagmar Waberski; Heiko Henning
Journal:  Biol Open       Date:  2016-11-15       Impact factor: 2.422

6.  Effect of long-term storage in Safe Cell+ extender on boar sperm DNA integrity and other key sperm parameters.

Authors:  Wiesław Bielas; Wojciech Niżański; Agnieszka Partyka; Anna Rząsa; Ryszard Mordak
Journal:  Acta Vet Scand       Date:  2017-09-11       Impact factor: 1.695

7.  Determination of a cooling-rate frame for antibiotic-free preservation of boar semen at 5°C.

Authors:  Aline F L Paschoal; Anne-Marie Luther; Helen Jäkel; Kathi Scheinpflug; Kristin Mühldorfer; Fernando P Bortolozzo; Dagmar Waberski
Journal:  PLoS One       Date:  2020-06-09       Impact factor: 3.240

8.  Integrity of Sperm Cell Membrane in the Semen of Crossbred and Purebred Boars during Storage at 17 °C: Heterosis Effects.

Authors:  Anna Wysokińska; Dorota Szablicka
Journal:  Animals (Basel)       Date:  2021-11-25       Impact factor: 2.752

  8 in total

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