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莫达非尼对大鼠随意皮瓣模型中皮瓣存活的保护作用:三磷酸腺苷敏感性钾通道和一氧化氮通路的作用。

Protective effect of modafinil on skin flap survival in the experimental random-pattern skin flap model in rats: The role of ATP-sensitive potassium channels and nitric oxide pathway.

机构信息

Experimental Medicine Research Center, Tehran University of Medical Sciences, Tehran, Iran; Department of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.

Department of Surgery, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

J Plast Reconstr Aesthet Surg. 2021 Jun;74(6):1346-1354. doi: 10.1016/j.bjps.2020.10.084. Epub 2020 Nov 10.

Abstract

BACKGROUND

The brain-stimulating agent modafinil acts through nitric oxide (NO) and adenosine triphosphate (ATP)-sensitive potassium (K) channels, involved in the skin flap survival (SFS). The main aim of this study was to investigate the efficacy of modafinil on SFS in rats through the involvement of NO pathway and K channels.

METHODS

Using controlled experiment study design, we enrolled a sample of Wistar male rats. Different doses of modafinil (10, 25, 50, and 100 mg/kg) were injected intraperitoneally (i.p.) before the surgery. L-NAME (non-selective nitric oxide synthase [NOS] inhibitor), aminoguanidine (inducible NOS inhibitor), and 7-nitroindazole (neuronal NOS inhibitor) were administered prior to modafinil. The role of K channels was determined by coadministering glibenclamide (K channel blocker) or cromakalim (K channel opener) with modafinil. The predictor variables were administration of different doses of modafinil, and the coadministration of modafinil with L-NAME, aminoguanidine, 7-nitroindazole, glibenclamide, and cromakalim. The main outcome variables included the percentage of necrotic area (PNA) in flap tissues, histopathological results, vascular endothelial growth factor (VEGF) immunohistochemical (IHC) staining, and nitrite concentrations. Appropriate statistics were computed considering p-value ≤ 0.05 significant.

RESULTS

Modafinil 25 mg/kg was the most effective dose (PNA: 26 [95% CI: 19-33]) vs. control (PNA: 81 [95% CI: 71-92]) (p< 0.001). All NOS inhibitors significantly reversed the protective effect of modafinil (p< 0.001). Non-effective dose of cromakalim had a synergistic effect with the sub-effective dose of modafinil (10 mg/kg), while glibenclamide reversed the effect of modafinil 25 mg/kg (p< 0.001).

CONCLUSIONS

Modafinil increases SFS mediated by NO pathway and K channels, which could therefore be a target to improve SFS.

摘要

背景

刺激大脑的药物莫达非尼通过一氧化氮(NO)和三磷酸腺苷(ATP)敏感的钾(K)通道起作用,这些通道与皮瓣存活(SFS)有关。本研究的主要目的是通过涉及 NO 途径和 K 通道来研究莫达非尼对大鼠 SFS 的疗效。

方法

采用对照实验研究设计,我们招募了一组 Wistar 雄性大鼠。莫达非尼(10、25、50 和 100mg/kg)以不同剂量腹腔内(i.p.)注射,在手术前给药。L-NAME(非选择性一氧化氮合酶[NOS]抑制剂)、氨基胍(诱导型 NOS 抑制剂)和 7-硝基吲唑(神经元型 NOS 抑制剂)在给予莫达非尼之前给予。通过与莫达非尼共同给予格列本脲(K 通道阻滞剂)或克罗卡林(K 通道开放剂)来确定 K 通道的作用。预测变量是给予不同剂量的莫达非尼,以及莫达非尼与 L-NAME、氨基胍、7-硝基吲唑、格列本脲和克罗卡林共同给药。主要的结果变量包括皮瓣组织中坏死面积的百分比(PNA)、组织病理学结果、血管内皮生长因子(VEGF)免疫组织化学(IHC)染色和亚硝酸盐浓度。考虑到 p 值≤0.05 有统计学意义,计算了适当的统计数据。

结果

莫达非尼 25mg/kg 是最有效的剂量(PNA:26 [95%CI:19-33]),与对照组(PNA:81 [95%CI:71-92])相比(p<0.001)。所有 NOS 抑制剂均显著逆转了莫达非尼的保护作用(p<0.001)。非有效剂量的克罗卡林与莫达非尼的亚有效剂量(10mg/kg)具有协同作用,而格列本脲逆转了莫达非尼 25mg/kg 的作用(p<0.001)。

结论

莫达非尼通过 NO 途径和 K 通道增加 SFS,因此可以成为改善 SFS 的靶点。

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