Dokucu Ali Ihsan, Ozturk Hulya, Ozturk Hayrettin, Tuncer Mehmet Cudi, Yilmaz Fahri
Department of Pediatric Surgery, Sisli Etfal Training and Research Hospital, Istanbul, Turkey.
Int Urol Nephrol. 2009;41(1):101-8. doi: 10.1007/s11255-008-9460-6. Epub 2008 Sep 12.
This study was designed to determine the effect of molsidomine (MO), a precursor of nitric oxide (NO) donor, on hypoxia inducible factor alpha (HIF-1alpha) and Sonic hedgehog (Shh) levels considered to be involved in the development of testes ischemia/reperfusion (I-R) injury. Torsions were created by rotating ipsilateral testes 720 degrees in a clockwise direction for 6 h and 1-h detorsion of the testis was performed. A sham operation was performed in group 1 (control, n = 7). In group 2 (I-R/Untreated, n = 7), following 6 h of unilateral testicular torsion, 1-h detorsion of the testis was performed. No drug was given. In group 3 (I-R/MO), after performing the same surgical procedure as in group 2, a NO donor MO was given at the starting time of reperfusion. In group 4 (I-R/L-NAME), after performing the same surgical procedure as in group 2, L-NAME was given at the starting time of reperfusion. Testes malondialdehyde (MDA) levels were determined as well as examining the testes histologically. Treatment of rats with MO produced a significant reduction in the levels of MDA and histopathological score compared to testes I-R groups. The Sonic hedgehog (Shh) expression in the basement membrane of the tubuli seminiferi, and sertoli and germinal cells in testicular tissue, were greatly increased in the I-R/MO group compared to groups 1, 2 and 4. Additionally, the HIF-1alpha expression in the interstitial spaces in testicular tissue were greatly increased in the I-R/MO group. The results suggest that MO has a protective effect against ischemia/reperfusion injury in rat testes and may affect Shh and HIF-1alpha signaling pathway.
本研究旨在确定一氧化氮(NO)供体前体吗多明(MO)对缺氧诱导因子α(HIF-1α)和音猬因子(Shh)水平的影响,这些因子被认为与睾丸缺血/再灌注(I-R)损伤的发生发展有关。通过将同侧睾丸顺时针旋转720度6小时造成扭转,并进行1小时的睾丸扭转复位。第1组(对照组,n = 7)进行假手术。第2组(I-R/未治疗组,n = 7),单侧睾丸扭转6小时后,进行1小时的睾丸扭转复位,未给予药物。第3组(I-R/MO组),在进行与第2组相同的手术操作后,于再灌注开始时给予NO供体MO。第4组(I-R/L-NAME组),在进行与第2组相同的手术操作后,于再灌注开始时给予L-NAME。测定睾丸丙二醛(MDA)水平,并对睾丸进行组织学检查。与睾丸I-R组相比,用MO治疗大鼠可使MDA水平和组织病理学评分显著降低。与第1、2和4组相比,I-R/MO组睾丸组织中曲细精管基底膜、支持细胞和生殖细胞中的音猬因子(Shh)表达显著增加。此外,I-R/MO组睾丸组织间质中的HIF-1α表达也显著增加。结果表明,MO对大鼠睾丸缺血/再灌注损伤具有保护作用,可能影响Shh和HIF-1α信号通路。