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Reproduction (Cambridge, England)2002; 124(5); 643-648;

Measured effect of collection and cooling conditions on the motility and the water transport parameters at subzero temperatures of equine spermatozoa.

Abstract: The effects of extracellular ice and cryoprotective agents on the measured volumetric shrinkage response and the membrane permeability parameters of equine spermatozoa have been reported previously. The volumetric shrinkage data were obtained using a differential scanning calorimeter technique that was independent of cell shape. The aim of this study was to examine the effects of collection and cooling conditions on the motility and the water transport parameters at subzero temperatures of equine spermatozoa. Stallion semen samples were collected using either a commercial lubricating agent, which caused osmotic stress to the spermatozoa, or water-insoluble Vaseline( trade mark ) as the artificial vagina lubricant. In some experiments, spermatozoa were cooled at 1 degrees C min(-1) from 20 degrees C to 4 degrees C to induce cold shock. An Equitainer was used to achieve control cooling rates ( 0 degrees C. The water transport response of spermatozoa that were cold-shocked and osmotically shocked was significantly different from that of control spermatozoa (P < 0.01). Osmotic stress appeared to have an effect on the water transport response, although this effect was not significant. These results indicate that cold shock alters the behaviour of equine spermatozoa in cryopreservation protocols as a result of changes in the water transport properties of the plasma membrane. Although osmotic stress did not significantly affect water transport in equine spermatozoa, it did significantly decrease sperm motility in the extended semen samples (P < 0.01), which would, in turn, lower the quality of cold-stored or cryopreserved spermatozoa.
Publication Date: 2002-11-06 PubMed ID: 12417002
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This study evaluates the impact of collection and cooling conditions on the movement and water transport parameters of horse sperm at below freezing temperatures. The researchers describe how cold shock and osmotic stress created by certain collection procedures can significantly change the water transport responses and motility of sperm, which in turn can affect the quality of samples that are cryopreserved or cold-stored.

Overview of the Study

  • The research was prompted by previous findings regarding the effects of exterior ice and cryoprotective agents on equine sperm’s volumetric shrinkage response and membrane permeability parameters.
  • The authors sought to determine how collection and refrigeration conditions influenced the motility and water transport characteristics of equine sperm at subzero temperatures.

Methodology

  • The stallion samples used in the study were collected employing either a commercial lubricant that caused osmotic stress to the sperm or an artificial vagina lubricated with water-insoluble Vaseline.
  • For some tests, the sperm was cooled at a rate of 1 degree Celsius per minute, from 20°C to 4°C to trigger a cold shock reaction.
  • They also used an Equitainer to maintain controlled cooling rates (≤ 0.3 degrees Celsius min-1) at temperatures greater than 0 degrees Celsius.

Findings

  • The research revealed that the water transport response in sperm specimens experiencing cold shock and osmotic stress significantly varied when compared to the control samples.
  • While osmotic stress was seen to affect the water transport response, this impact was not considerable enough to be statistically significant.
  • The study also found that osmotic stress led to a noticeable decrease in the motility of extended semen specimens, which could compromise the quality of cryopreserved or cold-stored sperm.

Conclusion

  • The study concluded that cold shock changes the behaviour of equine sperm in cryopreservation procedures due to modifications in the water transport characteristics of the plasma membrane.
  • Although osmotic stress did not significantly influence equine sperm water transport, it played a significant role in decreasing sperm motility, which could then lower the quality of cold-stored or cryopreserved sperm.

Cite This Article

APA
Devireddy RV, Swanlund DJ, Alghamdi AS, Duoos LA, Troedsson MH, Bischof JC, Roberts KP. (2002). Measured effect of collection and cooling conditions on the motility and the water transport parameters at subzero temperatures of equine spermatozoa. Reproduction, 124(5), 643-648.

Publication

ISSN: 1470-1626
NlmUniqueID: 100966036
Country: England
Language: English
Volume: 124
Issue: 5
Pages: 643-648

Researcher Affiliations

Devireddy, R V
  • Department of Mechanical Engineering, University of Minnesota, Minneapolis 55455, USA.
Swanlund, D J
    Alghamdi, A S
      Duoos, L A
        Troedsson, M H T
          Bischof, J C
            Roberts, K P

              MeSH Terms

              • Animals
              • Biological Transport
              • Cell Membrane / metabolism
              • Cryopreservation / methods
              • Cryopreservation / veterinary
              • Horses
              • Lubrication
              • Male
              • Semen Preservation / methods
              • Semen Preservation / veterinary
              • Specimen Handling
              • Sperm Motility
              • Spermatozoa / physiology
              • Water / metabolism

              Citations

              This article has been cited 4 times.
              1. Johnson S, Hall C, Das S, Devireddy R. Freezing of Solute-Laden Aqueous Solutions: Kinetics of Crystallization and Heat- and Mass-Transfer-Limited Model.. Bioengineering (Basel) 2022 Oct 10;9(10).
                doi: 10.3390/bioengineering9100540pubmed: 36290508google scholar: lookup
              2. Ros-Santaella JL, Domínguez-Rebolledo AE, Garde JJ. Sperm flagellum volume determines freezability in red deer spermatozoa.. PLoS One 2014;9(11):e112382.
                doi: 10.1371/journal.pone.0112382pubmed: 25380133google scholar: lookup
              3. Wolkers WF, Balasubramanian SK, Ongstad EL, Zec HC, Bischof JC. Effects of freezing on membranes and proteins in LNCaP prostate tumor cells.. Biochim Biophys Acta 2007 Mar;1768(3):728-36.
                doi: 10.1016/j.bbamem.2006.12.007pubmed: 17239814google scholar: lookup
              4. Thirumala S, Huang C, Dong Q, Tiersch TR, Devireddy RV. A theoretically estimated optimal cooling rate for the cryopreservation of sperm cells from a live-bearing fish, the green swordtail Xiphophorus helleri.. Theriogenology 2005 Jun;63(9):2395-415.