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  • Acrosin  (1)
  • Acrosomal membrane stability/disturbances  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Archives of dermatological research 273 (1982), S. 273-285 
    ISSN: 1432-069X
    Keywords: Acrosin ; Acrosome ; Acid extraction ; Snap freezing ; Physicochemical methods ; Zymogen activation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Washed human spermatozoa were subjected to different physicochemical methods, followed by acid extraction of the sperm acrosomes to dissolve acrosin. The acrosin activity of the sperm pellet and the supernatant was determined by benzoyl arginine ethyl ester/alcohol dehydrogenase (BAEE/ADH) assay to calculate the total acrosin activity in m U/106 spermatozoa. Membrane-active and zymogen-activating agents increased the total acrosin activity 50%–200% compared to acid extraction alone. Similar results were obtained by osmotic shock, sonication and treatment with glass beads. Snap freezing of unprotected spermatozoa in liquid nitrogen yielded a fivefold increase in total acrosin activity, thus demonstrating that this is the method of choice for optimal acrosin extraction. The possibility is discussed as to whether acrosomal membrane alterations with improved solubilization of membranebound acrosin and/or conformational changes and/or zymogen activation are responsible for the considerable increase observed in acrosin activity.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Archives of dermatological research 282 (1990), S. 335-342 
    ISSN: 1432-069X
    Keywords: Acrosin active, non-zymogen ; Proacrosin ; Acrosomal membrane stability/disturbances ; Fertility/sterility
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A spectrophotometric assay is described which, due to improved extraction conditions, allows quantitative determination of enzymatically active, non-zymogen acrosin, proacrosin and total acrosin activity from human sperm acrosomes. Acrosomal proteinase activity is assessed by acid extraction of the sperm pellet and the suspension medium before and after snap-freezing, followed by zymogen autoactivation. Release of acrosin from the acrosome can be used as a sensitive biochemical marker to characterize acrosomal membrane stability, severe disturbance of which may be the cause of impaired male fertility. Acrosin activities in different populations of semen specimens are reported and compared to data available in the literature. Different degrees of acrosomal membrane alterations are observed in men with oligozoospermia, teratozoospermia and polyzoospermia. Particularly in oligozoospermia, a significant increase of active, nonzymogen acrosin points to severe acrosomal membrane alterations and, in addition, to a premature activation of proacrosin, which may impair fertilization in certain individuals. Finally, acrosin activity is shown to be significantly influenced by the time of sexual abstinence. It is concluded that determination of acrosin may be a useful indicator of the fertility potential in men.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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