Shimizu S, Saito M, Dimitriadis F, Kinoshita Y, Shomori K, Satoh I, Satoh K
Division of Molecular Pharmacology, Department of Pathophysiological and Therapeutic Science, Tottori University School of Medicine, Yonago, Japan.
Int J Androl. 2011 Jun;34(3):268-75. doi: 10.1111/j.1365-2605.2010.01077.x.
The aim of this study was to investigate the effect of ischaemic post-conditioning (IPostC) against ischaemia-reperfusion (IR) injury on bilateral testes after unilateral testicular ischaemia in the rat. Eight-week-old male Sprague-Dawley rats were divided into control group; IR group (60 min ischaemia-24 h reperfusion); IPostC1 × 10 group (60 min ischaemia followed by one cycle of 10 sec reperfusion-10 sec ischaemia; then 24 h reperfusion); IPostC3 × 10 group (three cycles of 10 sec reperfusion-10 sec ischaemia; then 24 h reperfusion); IPostC5 × 10 group (five cycles of 10 sec reperfusion-10 sec ischaemia; then 24 h reperfusion) and IPostC3 × 30 group (three cycles of 30 sec reperfusion-30 sec ischaemia; then 24 h reperfusion). In the IR and IPostC groups, the right testicular vessels were clamped using a special vascular clip. Malondialdehyde (MDA) and myeloperoxidase (MPO) levels were measured in testicular tissue samples bilaterally. Additionally, bilateral testicular tissue samples were processed for histological evaluation including haematoxylin-eosin, 4-hydroxy-2-nonenal (4-HNE) and TdT-mediated dUTP Nick End Labelling (TUNEL) staining. The levels of MDA and MPO as well as the positive cells per seminiferous tubule in TUNEL and 4-HNE stain in bilateral testes from the IR group were significantly higher compared with the control group. IPostC3 × 30 protocol significantly ameliorated the aforesaid parameters in both testes compared with the IR group. For the first time, we have demonstrated that IPostC protects both testes after unilateral testicular ischaemia-reperfusion. IPostC3 × 30 protocol offered the most effective protection.
本研究旨在探讨缺血后处理(IPostC)对大鼠单侧睾丸缺血后双侧睾丸缺血再灌注(IR)损伤的影响。将8周龄雄性Sprague-Dawley大鼠分为对照组;IR组(60分钟缺血-24小时再灌注);IPostC1×10组(60分钟缺血后进行1个周期的10秒再灌注-10秒缺血;然后24小时再灌注);IPostC3×10组(3个周期的10秒再灌注-10秒缺血;然后24小时再灌注);IPostC5×10组(5个周期的10秒再灌注-10秒缺血;然后24小时再灌注)和IPostC3×30组(3个周期的30秒再灌注-30秒缺血;然后24小时再灌注)。在IR组和IPostC组中,使用特殊血管夹夹闭右侧睾丸血管。双侧测量睾丸组织样本中的丙二醛(MDA)和髓过氧化物酶(MPO)水平。此外,对双侧睾丸组织样本进行组织学评估,包括苏木精-伊红、4-羟基-2-壬烯醛(4-HNE)和TdT介导的dUTP缺口末端标记(TUNEL)染色。与对照组相比,IR组双侧睾丸中MDA和MPO水平以及TUNEL和4-HNE染色中每个生精小管的阳性细胞数显著更高。与IR组相比,IPostC3×30方案显著改善了双侧睾丸的上述参数。我们首次证明,IPostC可保护单侧睾丸缺血再灌注后的双侧睾丸。IPostC3×30方案提供了最有效的保护。