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From the Institute of Human Genetics, Polish Academy of Sciences, Poznan, Poland.
| Correspondence to: Dr Maciej Kurpisz, Professor, Institute of Human Genetics, Polish Academy of Sciences, Strzeszynska 32, 60-479 Poznan, Poland (e-mail: kurpimac{at}man.poznan.pl). |
), used singly or in combinations, were
analyzed. WBCs were isolated from the whole heparinized blood using a density
gradient technique (Histopaque 1.077). Spermatozoa were isolated from semen
samples with normal sperm parameters by both the swim-up technique (swim-up
fraction) and by a discontinuous Percoll gradient centrifugation (90% and 47%
Percoll fractions). Peroxidative damage to sperm membrane lipids was assessed
by determining the concentration of malondialdehyde (MDA) in lysates of
spermatozoa using high-performance liquid chromatography (HPLC). There were no
statistically significant differences in MDA concentrations between sperm
fractions incubated with cytokines and respective controls (spermatozoa
alone). In spermatozoa isolated by the swim-up technique, the MDA level was
significantly higher only after incubation with IL-6 and IL-8 plus WBCs when
compared to sperm incubated with leukocytes alone (0.62 ± 0.21
µmol/L and 0.42 ± 0.22 µmol/L, respectively; P <
.05). In spermatozoa recovered from the 47% Percoll, only a combination of
IL-12 and IL-18 used together with WBCs was linked with a significant increase
in MDA concentration (from 0.41 ± 0.13 µmol/L to 0.65 ± 0.19
µmol/L; P < .05). The results obtained suggest that cytokines
produced during the inflammatory process intensify the level of oxidative
stress caused by leukocytes, which may have serious consequences for sperm
membrane integrity.
Key words: Semen inflammation, peroxidative damage
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