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      Freezing and thawing alter chromatin stability of ejaculated human spermatozoa: fluorescence acridine orange staining and Feulgen-DNA cytophotometric studies.

      Gamete research
      Acridine Orange, diagnostic use, Adult, Chromatin, abnormalities, Cytophotometry, methods, DNA, analysis, Freezing, Humans, Male, Spermatozoa, Staining and Labeling

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          Abstract

          Cryopreservation and freezing-thawing effects on the fertilizing ability of human spermatozoa commonly are evaluated by post-thaw motility. Various studies have depicted the ultrastructural changes caused by freezing-thawing, yet the chromatin alterations have been studied very limitedly. Our aim was to determine the extent to which freezing-thawing alters the chromatin of human spermatozoa, using two analytical methods: acridine orange staining and Feulgen-DNA cytophotometric studies. Both methods revealed a dramatic effect of freezing-thawing on sperm chromatin: the native DNA content decreased as did the Feulgen-DNA content, and sperm surface area was reduced. These results indicate an effect on DNA, diminished accessibility for Feulgen, and a decrease in nuclear surface area and prompt us to hypothesize a relationship between an "overcondensation" state for sperm chromatin after freezing-thawing and a lower conception rate for human semen after cryostorage.

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          Author and article information

          Journal
          2465984
          10.1002/mrd.1120210107

          Chemistry
          Acridine Orange,diagnostic use,Adult,Chromatin,abnormalities,Cytophotometry,methods,DNA,analysis,Freezing,Humans,Male,Spermatozoa,Staining and Labeling

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