Representative Office Richter Gedeon Serbia, Belgrade, Serbia.
University of Kragujevac, Faculty of Medical Sciences, Department of Pharmacy, Kragujevac, Serbia.
Oxid Med Cell Longev. 2020 Feb 10;2020:6361703. doi: 10.1155/2020/6361703. eCollection 2020.
Taken into consideration that oxidative stress response after preconditioning with phosphodiesterase inhibitors (PDEIs) and moderate physical activity has still not been clarified, the aim of this study was to assess the effects of PDEIs alone or in combination with physical activity, on systemic redox status. The study was carried out on 96 male rats classified into two groups. The first group included animals exposed only to pharmacological preconditioning (PreC) maneuver (sedentary control (CTRL, 1 ml/day saline, = 12), nicardipine (6 mg/kg/day of NIC, = 12), vinpocetine (10 mg/kg/day of VIN, = 12), and nimodipine (NIM 10 mg/kg/day of, = 12). The second included animals exposed to preconditioning with moderate-intensity training (MIT) on treadmill for 8 weeks. After 5 weeks from the start of training, the animals were divided into four subgroups depending on the medication to be used for pharmacological PreC: moderate-intensity training (MIT+ 1 ml/day saline, = 12), nicardipine (MIT+ 6 mg/kg/day of NIC, = 12), vinpocetine (MIT+ 10 mg/kg/day of VIN, = 12), and nimodipine (MIT+ 10 mg/kg/day of NIM, = 12). After three weeks of pharmacological preconditioning, the animals were sacrificed. The following oxidative stress parameters were measured spectrophotometrically: nitrites (NO ), superoxide anion radical (O ), hydrogen peroxide (HO), index of lipid peroxidation (TBARS), superoxide dismutase (SOD), catalase (CAT), and reduced glutathione (GSH). Our results showed that PDE1 and MIT preconditioning decreased the release of prooxidants and improved the activity of antioxidant enzymes thus preventing systemic oxidative stress.
考虑到磷酸二酯酶抑制剂 (PDEIs) 和适度体力活动预处理后的氧化应激反应尚未阐明,本研究旨在评估 PDEIs 单独或与体力活动联合使用对全身氧化还原状态的影响。该研究在 96 只雄性大鼠上进行,分为两组。第一组包括仅接受药物预处理 (PreC) 操作的动物(久坐对照 (CTRL,1 ml/天盐水, = 12)、尼卡地平 (6 mg/kg/天 NIC, = 12)、长春西汀 (10 mg/kg/天 VIN, = 12) 和尼莫地平(NIM 10 mg/kg/天, = 12)。第二组包括在跑步机上进行 8 周中等强度训练 (MIT) 的动物。训练开始后 5 周,根据用于药物预处理的药物将动物分为四个亚组:中等强度训练 (MIT+1 ml/天盐水, = 12)、尼卡地平 (MIT+6 mg/kg/天 NIC, = 12)、长春西汀 (MIT+10 mg/kg/天 VIN, = 12) 和尼莫地平(MIT+10 mg/kg/天 NIM, = 12)。药物预处理三周后,处死动物。采用分光光度法测定以下氧化应激参数:亚硝酸盐 (NO 2-)、超氧阴离子自由基 (O 2-)、过氧化氢 (HO 2-)、脂质过氧化指数 (TBARS)、超氧化物歧化酶 (SOD)、过氧化氢酶 (CAT) 和还原型谷胱甘肽 (GSH)。我们的结果表明,PDE1 和 MIT 预处理可减少促氧化剂的释放并提高抗氧化酶的活性,从而防止全身氧化应激。