AI Article Synopsis

  • The study aimed to examine oxidative stress (OS) parameters in adult rats after testicular torsion and detorsion.
  • The experiment involved four groups of male Wistar rats, with variations in testicular torsion and subsequent procedures, and oxidative stress markers were assessed in both testicular tissue and plasma after 30 days.
  • Results indicated that testicular torsion and detorsion lead to increased oxidative stress markers, with significant differences noted between testis sides and groups, suggesting that ischemia/reperfusion alters the testicular tissue's oxidant-antioxidant balance.

Article Abstract

Background: The aim of this study was to determine oxidative stress (OS) parameters after testicular torsion/detorsion in adult rats.

Materials And Methods: In this experimental study, male adult Wistar rats were divided into four groups, each consisting of seven animals: group I-one hour right testicular torsion with subsequent orchiectomy, group II-one hour right testicular torsion followed by detorsion, group III-unilateral right-sided orchiectomy without previous torsion and group IV-control. After 30 days, bilateral orchiectomies were performed in rats with both testes and unilateral orchiectomies in rats with single testicles. Parameters of OS were determined in testicular tissue and in plasma.

Results: Plasma concentrations of advanced oxidation protein products (AOPP) and thiobarbituric acid reactive substances (TBARS) were higher (p<0.05 and p<0.01, respectively), whilst the plasma concentration of the total sulfhydryl (T-SH)-groups was lower (p<0.05) in group I compared to the control group. Group II had higher plasma concentrations of AOPP compared to group IV (p<0.05), as well as significantly increased TBARS and decreased T-SH-group levels compared to groups III (p<0.05 and p<0.01, respectively) and IV (p<0.01, for both parameters). There were significant differences in OS markers between the ipsilateral and contralateral testis, as well as significant correlations among levels of both plasma and tissue markers of OS.

Conclusion: The increase in TBARS levels seen throughout the experimental period indicated that OS development was caused by ischemia/reperfusion in the testicular tissue. The oxidant-antioxidant system of the testicular tissue was altered during torsion as well as detorsion.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4410030PMC
http://dx.doi.org/10.22074/ijfs.2015.4216DOI Listing

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