a Department of Sport Physiology, Faculty of Sport Sciences, Shahid Rajaee Teacher Training University, PO box 16875-163, Tehran, Iran.
b NeuroBiology Research Center, Shahid Beheshti University of Medical Sciences, PO box 19615-1178, Tehran, Iran.
Appl Physiol Nutr Metab. 2018 Jan;43(1):45-53. doi: 10.1139/apnm-2017-0313. Epub 2017 Aug 30.
This study aimed to investigate the effect of exercise and nitric oxide synthase (NOS) inhibition on memory, anxiety, and protein levels of brain-derived neurotrophic factor (BDNF) and P70S6 kinase (P70S6K). Twenty-month-old rats were divided into 6 groups: a control group, 2 groups treated with l-nitro-arginine methyl ester (L-NAME) (25 or 100 mg/kg) for 63 days, 2 groups treated with L-NAME (25 or 100 mg/kg) for 63 days plus 2 months of exercise, and 1 group treated with exercise. Behavioral tests were conducted to determine the anxiolytic and memory-improving role of exercise and NOS inhibition. BDNF, P70S6K, and cleaved caspase-3 protein levels in the hippocampus and prefrontal cortex were evaluated by Western blotting. Exercise and L-NAME (25 mg/kg) or their combination had an anxiolytic effect and improved spatial memory in old rats compared with the control or exercised group, respectively. Exercise and treatment with a low dose of L-NAME (25 mg/kg) each increased BDNF and P70S6K in the hippocampus and prefrontal cortex compared with levels in control rats. In comparison with exercise alone, co-treatment with exercise and a low dose of L-NAME (25 mg/kg) also increased BDNF and P70S6K in the hippocampus. The neuronal level of cleaved caspase-3 was reduced in the L-NAME (25 mg/kg) + exercise group compared with the exercised group. The L-NAME (100 mg/kg) + exercise treatment had no positive behavioral or molecular effects compared with exercise alone. The protective role of NOS inhibition and aerobic exercise against aging is probably modulated via BDNF and P70S6K in the brain.
本研究旨在探讨运动和一氧化氮合酶(NOS)抑制对记忆、焦虑以及脑源性神经营养因子(BDNF)和 P70S6 激酶(P70S6K)蛋白水平的影响。将 20 月龄大鼠分为 6 组:对照组、2 组给予 L-硝基精氨酸甲酯(L-NAME)(25 或 100mg/kg)处理 63 天、2 组给予 L-NAME(25 或 100mg/kg)处理 63 天加 2 个月运动、1 组给予运动。通过行为测试确定运动和 NOS 抑制对焦虑和记忆改善的作用。通过 Western blot 评估海马体和前额叶皮质中 BDNF、P70S6K 和裂解的半胱天冬酶-3 蛋白水平。与对照组或运动组相比,运动和 L-NAME(25mg/kg)或两者的组合对老年大鼠具有抗焦虑作用并改善空间记忆。与对照组相比,运动和低剂量 L-NAME(25mg/kg)处理均可增加海马体和前额叶皮质中的 BDNF 和 P70S6K。与单独运动相比,运动和低剂量 L-NAME(25mg/kg)联合治疗还增加了海马体中的 BDNF 和 P70S6K。与运动组相比,L-NAME(25mg/kg)+运动组中神经元裂解的半胱天冬酶-3 水平降低。与单独运动相比,L-NAME(100mg/kg)+运动治疗在行为和分子方面没有积极作用。NOS 抑制和有氧运动对衰老的保护作用可能通过大脑中的 BDNF 和 P70S6K 来调节。