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Supplementing post‐wash asthenozoospermic human spermatozoa with coenzyme Q10 for 1 hr in vitro improves sperm motility, but not oxidative stress
Author(s) -
Boonsimma Keathisak,
Ngeamvijawat Jiraporn,
Sukcharoen Nares,
Boonla Chanchai
Publication year - 2020
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/and.13818
Subject(s) - asthenozoospermia , andrology , semen , coenzyme q10 , sperm motility , sperm , motility , oxidative stress , biology , semen analysis , percoll , male infertility , endocrinology , in vitro , biochemistry , infertility , medicine , pregnancy , microbiology and biotechnology , genetics
We investigated the effect of supplementing post‐wash asthenozoospermic spermatozoa with coenzyme Q10 (CoQ10) in vitro, which may reduce oxidative stress and improve sperm motility. Semen samples were collected from 39 men with asthenozoospermia, and their spermatozoa were isolated by two‐layer Percoll density‐gradient centrifugation. Kinetic parameters of the isolated spermatozoa (baseline before intervention) were determined immediately by computer‐aided semen analysis. Total anti‐oxidant capacity and protein carbonyl levels, as markers of oxidative stress, were also measured in the baseline spermatozoa. The baseline spermatozoa suspension was divided equally into two portions, one for CoQ10 supplementation (50 µg/ml for 1 hr) and the other as an un‐supplemented vehicle control. The total motility of the CoQ10‐supplemented spermatozoa was significantly higher than in the control ( p  = .009) and progressive motility tended to be higher ( p =  .053). Immotile sperm concentration in the CoQ10‐supplemented spermatozoa was significantly lower than in both the baseline ( p  = .026) and control ( p  = .009). Total anti‐oxidant capacity and protein carbonyl levels between the baseline, CoQ10‐supplemented and control spermatozoa were not significantly different. Our data suggest that CoQ10 treatment reactivated sperm motility. We propose short‐term supplementation of post‐wash asthenozoospermic spermatozoa with CoQ10 before intrauterine insemination.

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