Premium
Lipid peroxidation in human spermatozoa and maintenance of progressive sperm motility
Author(s) -
Engel S.,
Schreiner Th.,
Petzoldt R.
Publication year - 1999
Publication title -
andrologia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.633
H-Index - 59
eISSN - 1439-0272
pISSN - 0303-4569
DOI - 10.1111/j.1439-0272.1999.tb02837.x
Subject(s) - tbars , motility , incubation , lipid peroxidation , thiobarbituric acid , sperm motility , andrology , chemistry , sperm , biochemistry , endocrinology , biology , antioxidant , medicine , microbiology and biotechnology
Summary. Washed and deep frozen spermatozoa of 46 patients from an infertility clinic were separated into 3 different groups depending on their progressive motility (expressed as the sperm motile efficiency index according to Ishii et al. , 1977), determined 0 and 3 h after liquefaction, and were examined for their lipid peroxidation (LPO) potential by means of the thiobarbituric acid assay. Spontaneous and iron‐catalysed generation (after 15, 30 and 60 min incubation) of thiobarbituric acid‐reactive substances (TBARS) was measured spectrophotometrically. Spontaneous LPO revealed the highest generation of TBARS in the group of spermatozoa with initially normal progressive motility and decreased maintenance of progressive motility after 3 h of aerobic incubation. Iron‐catalysed LPO generally revealed the highest amounts of TBARS after 60 min, especially in the aforementioned group with decreased motility maintenance. The differences between this group and the two other groups were highly significant. Consequently, spermatozoa with initially normal progressive motility but decreased maintenance of motility, generated higher amounts of stable LPO products than others, which suggests that loss of motility under aerobic incubation seems to be the consequence of enhanced LPO processes.