罗氟司特对大鼠缺血/再灌注引起的肾损伤具有雷诺保护作用:生化和组织学研究的证据

Rehab F. Abdel-Rahman , Marawan A. Elbaset , Hany M. Fayed , Tuba Esatbeyoglu , Sherif M. Afifi , Rehab Adel Diab
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引用次数: 0

摘要

氧化应激、炎症和细胞凋亡是造成肾缺血再灌注(I/R)损伤的主要因素。本研究旨在探讨预处理 PDE4 抑制剂罗氟司特(Rof)对肾缺血再灌注损伤的影响及其潜在机制。对 Sprague-Dawley 大鼠进行 30 分钟的单侧肾缺血,然后进行 45 分钟的再灌注。在诱导 I/R 前给大鼠注射 Rof(1.5 和 3 mg/kg)七天。研究结果表明,通过降低血尿素氮和肌酐水平,Rof能明显减轻肾脏损伤,且具有剂量依赖性。Rof 还具有抗氧化和抗炎作用,这体现在谷胱甘肽和丙二醛水平的改善以及促炎细胞因子(IL-6 和 TNF-α)的减少。此外,Rof 还阻止了 HO-1 和 Nrf2 表达的下调。这些结果表明,Rof疗法可通过其抗氧化和抗炎特性保护肾脏免受I/R诱导的损伤,为治疗肾脏I/R损伤提供了一种潜在的治疗方法。
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Reno-protective effect of Roflumilast against kidney injury induced by ischemia/reperfusion in rats: Evidence from biochemical and histological investigations

Oxidative stress, inflammation, and apoptosis are major contributors to renal ischemia/reperfusion (I/R) injury. This study aimed to investigate the effects of pretreatment with the PDE4 inhibitor roflumilast (Rof) on renal I/R and its underlying mechanisms. Sprague-Dawley rats were subjected to 30 minutes of unilateral renal ischemia followed by 45 minutes of reperfusion. Rof (1.5 and 3 mg/kg) was administered for seven days prior to I/R induction. The findings showed that Rof significantly and dose-dependently attenuated kidney damage by reducing blood urea nitrogen and creatinine levels. Rof also exhibited antioxidant and anti-inflammatory effects, as evidenced by improved glutathione and malondialdehyde levels and decreased proinflammatory cytokines (IL-6 and TNF-α). Furthermore, Rof prevented the downregulation of HO-1 and Nrf2 expression. These results suggest that Rof therapy could protect the kidneys from I/R-induced injury through its antioxidant and anti-inflammatory properties, providing a potential therapeutic approach for the management of renal I/R damage.

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