Literature DB >> 11780916

Detection of DNA damage in response to cooling injury in equine spermatozoa using single-cell gel electrophoresis.

Jennifer J Linfor1, Stuart A Meyers.   

Abstract

Single-cell gel electrophoresis (SCGE), or comet assay, has the ability to detect damage at the single cell level and has not been reported for equine sperm. The ability to detect nuclear damage at the single cell level could aid in the advancement of protocols for optimal semen preservation. The goals of these experiments were to adapt this assay for use with equine sperm and to utilize the assay for determining the integrity of equine sperm DNA following treatments with storage at various decreased temperatures (-20 degrees C and 5 degrees C). Results from experiments in which sperm were frozen (-20 degrees C) in the absence of cryoprotectants revealed that significantly more cells with fragmented tails of DNA, or comets, occurred among those exposed to 1, 3, and 5 freeze-thaw cycles (65% +/- 6%, 76% +/- 11%, 92% +/- 6%, respectively) compared with fresh, untreated sperm (19% +/- 16%, P < .05). In addition DNA damage was different (P < .05) between the three freeze-thaw treatments. Sensitivity of SCGE on equine sperm was further tested with known ratios of frozen-thawed and fresh cells. The amount of detectable DNA damage was positively correlated with the percentage of cryo-damaged cells in each treatment (r2 = 0.92, P < .05). Potential damage as a result of cooled storage was also investigated and results revealed that sperm stored for 48 hours (at 5 degrees C) had a higher percentage of comets than that of fresh sperm (63% +/- 13.9% and 28% +/- 15.6%, respectively, P < .05). The percentage of viable sperm also decreased linearly over time and was inversely correlated with percent of comets (r2 = 0.805, P < .001). Detection of sublethal and/or uncompensable fertility factors in semen, such as DNA fragmentation, could be useful for detecting male differences in semen for cooling or cryopreservation potential and could provide a tool for monitoring and preserving fertility for individual stallions.

Entities:  

Mesh:

Year:  2002        PMID: 11780916     DOI: 10.1002/j.1939-4640.2002.tb02603.x

Source DB:  PubMed          Journal:  J Androl        ISSN: 0196-3635


  4 in total

1.  Mutant mice derived by ICSI of evaporatively dried spermatozoa exhibit expected phenotype.

Authors:  Ming-Wen Li; Brian Baridon; Amanda Trainor; Esi Djan; Amanda Koehne; Stephen M Griffey; John D Biggers; Mehmet Toner; K C Kent Lloyd
Journal:  Reproduction       Date:  2012-01-24       Impact factor: 3.906

2.  Cryomacroscopy of vitrification, Part II: Experimental observations and analysis of fracture formation in vitrified VS55 and DP6.

Authors:  Paul S Steif; Matthew Palastro; Chen-Rei Wan; Simona Baicu; Michael J Taylor; Yoed Rabin
Journal:  Cell Preserv Technol       Date:  2005-09

3.  Methods for cryopreservation of guinea fowl sperm.

Authors:  Éva Váradi; Barbara Végi; Krisztina Liptói; Judit Barna
Journal:  PLoS One       Date:  2013-04-29       Impact factor: 3.240

4.  The effect of two pre-cryopreservation single layer colloidal centrifugation protocols in combination with different freezing extenders on the fragmentation dynamics of thawed equine sperm DNA.

Authors:  Luna Gutiérrez-Cepeda; Alvaro Fernández; Francisco Crespo; Miguel Ángel Ramírez; Jaime Gosálvez; Consuelo Serres
Journal:  Acta Vet Scand       Date:  2012-12-05       Impact factor: 1.695

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.