沙芬可改善睾丸扭转-扭转模型大鼠睾丸缺血-再灌注损伤。

Revista internacional de andrologia Pub Date : 2024-12-01 Epub Date: 2024-12-30 DOI:10.22514/j.androl.2024.028
Si-Ming Wei, Yu-Min Huang
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引用次数: 0

摘要

背景:睾丸扭转-扭转损伤是一种常见的由活性氧过量引起的缺血-再灌注损伤。活性氧可能通过调节基因表达影响细胞分化。热休克蛋白70-2 (HSP70-2)基因在睾丸中的表达对精子发生至关重要。番红花醛是从藏红花中分离得到的主要生物活性成分,具有较强的抗氧化活性。我们目前的研究考察了safranal保护睾丸免受缺血再灌注损伤的潜在机制。方法:雄性Sprague-Dawley大鼠60只,随机分为假手术对照组、睾丸缺血再灌注组和沙非那尔治疗组。左睾丸逆时针旋转720°,维持2小时,达到睾丸缺血。扭转左睾丸反向旋转至其自然位置,形成再灌注。沙番那治疗组大鼠在再灌注开始时腹腔注射沙番那。切除睾丸,检测丙二醛(一种敏感的活性氧指标)的含量、HSP70-2蛋白的表达和睾丸生精活性。结果:与对照组相比,单侧睾丸缺血再灌注显著增加同侧睾丸丙二醛水平。显著降低了HSP70-2蛋白的表达和生精活性(p < 0.001)。此外,我们的研究发现,与睾丸缺血再灌注组相比,萨芬那治疗组同侧睾丸丙二醛水平显著降低,HSP70-2表达水平和生精功能水平显著升高(p < 0.01)。结论:红花醛通过降低活性氧水平,提高HSP70-2表达,对睾丸扭转/扭转所致的缺血再灌注损伤具有保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Safranal ameliorates testicular ischemia-reperfusion injury in testicular torsion-detorsion rat model.

Background: Testicular torsion-detorsion damage is a common ischemia-reperfusion injury brought on by an excess of reactive oxygen species. Reactive oxygen species may affect cellular differentiation by regulating gene expression. The heat shock protein 70-2 (HSP70-2) gene expression in the testis is essential for spermatogenesis. Safranal, the main bioactive ingredient isolated from Crocus sativus L., has potent antioxidant properties. Our current investigation examined the potential mechanism by which safranal could shield the testis from ischemia-reperfusion damage.

Methods: Sixty Sprague-Dawley male rats were randomly assigned into the sham-operated control group, testicular ischemia-reperfusion group, and safranal-treated group. Testicular ischemia was achieved by twisting the left testis 720° counterclockwise and maintained for two hours. Reperfusion was created by counter-rotating the torsional left testis to its natural position. Rats in the safranal-treated group received an intraperitoneal injection of safranal at the onset of reperfusion. Testes were excised to examine the quantity of malondialdehyde (a sensitive indicator of reactive oxygen species), expression of the HSP70-2 protein, and the testicular spermatogenic activity.

Results: Unilateral testicular ischemia-reperfusion significantly increased the levels of malondialdehyde in the ipsilateral testes compared to the control group. It also significantly reduced the expression of HSP70-2 protein and spermatogenic activity (p < 0.001). In addition, our investigation revealed that, in comparison to the testicular ischemia-reperfusion group, the ipsilateral testes of the safranal-treated group had significantly lower levels of malondialdehyde and had significantly higher HSP70-2 expression and levels of spermatogenic function (p < 0.01).

Conclusions: These results suggest that via lowering reactive oxygen species levels and increasing HSP70-2 expression, safranal protects against testicular torsion/detorsion-induced ischemia/reperfusion injury.

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