Semen reactive oxygen species levels are correlated with erectile function among chronic prostatitis/chronic pelvic pain syndrome patients
Chronic Prostatitis/Chronic Pelvic Pain Syndrome (CP/CPPS) is often associated with erectile dysfunction (ED). However, the underlying pathophysiological mechanisms of ED occurrence are still unclear in patients with CP/CPPS. The aim of the study was to investigate superoxide anion (O 2 • − ) and to...
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Published in | International journal of impotence research Vol. 30; no. 6; pp. 335 - 341 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.11.2018
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
ISSN | 0955-9930 1476-5489 1476-5489 |
DOI | 10.1038/s41443-018-0047-1 |
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Summary: | Chronic Prostatitis/Chronic Pelvic Pain Syndrome (CP/CPPS) is often associated with erectile dysfunction (ED). However, the underlying pathophysiological mechanisms of ED occurrence are still unclear in patients with CP/CPPS. The aim of the study was to investigate superoxide anion (O
2
•
−
) and total reactive oxygen species (ROS) production in semen of men with category IIIA CP/CPPS and their association with ED. This prospective study included 33 men with category IIIA CP/CPPS. Control group consisted of 13 healthy men. Total ROS and O
2
•
−
production were assayed by luminol and lucigenin-dependent chemiluminescence (CL) methods, respectively. ED was evaluated using the IIEF-5 questionnaire. Patients with CP/CPPS had significantly higher seminal total ROS and O
2
•
−
levels than healthy control subjects (2.9 ± 0.5 relative light unit (RLU) vs. 2.4 ± 0.2 RLU,
p
< 0.001; luminol-dependent CL and 2.5 ± 0.4 RLU vs. 2.3 ± 0.2 RLU,
p
= 0.02; lucigenin-dependent CL, respectively). Seminal O
2
•
−
and ROS levels were negatively correlated with IIEF-5 scores (
r
= −0.556,
r
= −0.536;
p
< 0.001, respectively). These results may suggest O
2
•
−
/ROS overproduction could be one of the important mechanisms in the etiology of ED development in CP/CPPS patients. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 0955-9930 1476-5489 1476-5489 |
DOI: | 10.1038/s41443-018-0047-1 |