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Comparative evaluation of DNA integrity using sperm chromatin structure assay and Sperm-Ovis-Halomax during in vitro capacitation of cryopreserved ram spermatozoa.

Patricia Peris-FrauManuel Álvarez-RodriguezAlicia Martín-MaestroMaría Iniesta-CuerdaIrene Sánchez-AjofrínJosé Julián GardeHeriberto Rodriguez-MartinezMaría Del Rocío Fernández-Santos
Published in: Reproduction in domestic animals = Zuchthygiene (2020)
This study aimed to compare the ability of sperm chromatin structure assay (SCSA® ) and Sperm-Ovis-Halomax® to detect DNA fragmentation in frozen-thawed ram spermatozoa incubated under capacitating conditions in synthetic oviductal fluid (SOF) supplemented with oestrous sheep serum (SOF-ESS) at multiple time points (0-240 min). Incubation in SOF-ESS had no significant effects on SCSA® parameters while the percentage of spermatozoa with fragmented DNA measured by Sperm-Ovis-Halomax® increased after 180 min of incubation. In addition, no correlation or agreement was found between the techniques, suggesting that SCSA® and Sperm-Ovis-Halomax® may quantify different types of DNA damage in ram spermatozoa under these experimental conditions.
Keyphrases
  • dna damage
  • circulating tumor
  • single molecule
  • cell free
  • transcription factor
  • high throughput
  • genome wide
  • dna repair
  • mesenchymal stem cells
  • pregnant women
  • circulating tumor cells
  • umbilical cord