Department of Urology, Ondokuz Mayis University Faculty of Medicine, Samsun, Turkey.
Urology. 2010 Aug;76(2):507.e1-5. doi: 10.1016/j.urology.2010.03.074. Epub 2010 Jun 25.
We wanted to show early and late biochemical, histopathological, and apoptotic changes caused by unilateral spermatic cord torsion in ipsilateral and contralateral testicles and the effect of the poly (adenosine triphosphate-ribose) polymerase (PARP) inhibitor, nicotinamide, on these changes in early and late periods.
Forty-seven Wistar albino rats were divided into 2 major groups as early and late periods. Subsequently, each group was divided into subgroups as control, sham, torsion-detorsion (TD), TD treated with saline (TDS), and TD treated with nicotinamide (TDN). Left testicles were subjected to spermatic cord torsion for 4 hours. Thirty-minutes before detorsion, 0.2 mL saline or 10 mg/kg nicotinamide was administered intraperitoneally to the TDS and TDN groups, respectively. Bilateral orchidectomy was performed by the end of the fourth hour in early and 2 months after TD in late groups and the animals were sacrificed. Apoptosis, Johnsen Tubular Biopsy Score, and seminiferous tubule diameter (STD) were used to evaluate histopathological changes. Ischemia-reperfusion injury-related changes were assessed by levels of malondialdehyde (MDA) and total and free glutathione in serum.
There were no significant differences between groups in terms of serum MDA and total and free glutathione levels. Rats given nicotinamide had a higher number of spermatogonia in seminiferous tubules in early and late periods when compared with the untreated group (P <.05). In early and late groups, mean STD of contralateral and ipsilateral testicles were higher in rats given nicotinamide when compared with untreated groups. No significance was observed in terms of STD between early and late groups. Late groups treated with nicotinamide had less apoptosis when compared with untreated groups (P <.05).
Nicotinamide may successfully decrease ischemia-reperfusion injury in early and late periods in both testicles.
本研究旨在展示单侧精索扭转导致同侧和对侧睾丸早期和晚期生化、组织病理学和细胞凋亡变化,以及聚(腺嘌呤二核苷酸-核糖)聚合酶(PARP)抑制剂烟酰胺对这些变化的早期和晚期影响。
47 只 Wistar 白化大鼠分为早期和晚期 2 个主要组。随后,每个组又分为对照组、假手术组、扭转-复位(TD)组、TD 生理盐水处理组(TDS)和 TD 烟酰胺处理组(TDN)。左侧睾丸精索扭转 4 小时。在复位前 30 分钟,分别向 TDS 和 TDN 组大鼠腹腔内注射 0.2 mL 生理盐水或 10 mg/kg 烟酰胺。早期组在第 4 小时结束时行双侧睾丸切除术,晚期组在 TD 后 2 个月行双侧睾丸切除术,然后处死动物。采用凋亡、Johnsen 管状活检评分和生精小管直径(STD)评估组织病理学变化。通过血清丙二醛(MDA)和总、游离谷胱甘肽水平评估缺血再灌注损伤相关变化。
各组血清 MDA 及总、游离谷胱甘肽水平无显著差异。与未处理组相比,早期和晚期给予烟酰胺的大鼠生精小管内精原细胞数量更多(P<.05)。与未处理组相比,早期和晚期给予烟酰胺的大鼠对侧和同侧睾丸的平均 STD 更高(P<.05)。早期和晚期组间 STD 无显著差异。与未处理组相比,晚期给予烟酰胺的大鼠凋亡较少(P<.05)。
烟酰胺可成功减轻早期和晚期双侧睾丸的缺血再灌注损伤。