Exercise training with concomitant nitric oxide synthase inhibition improved anxiogenic behavior, spatial cognition, and BDNF/P70S6 kinase activation in 20-month-old rats

Author:

Salehpour Mojtaba1,Khodagholi Fariba2,Zeinaddini Meymand Arman3,Nourshahi Maryam4,Ashabi Ghorbangol5

Affiliation:

1. Department of Sport Physiology, Faculty of Sport Sciences, Shahid Rajaee Teacher Training University, PO box 16875-163, Tehran, Iran.

2. NeuroBiology Research Center, Shahid Beheshti University of Medical Sciences, PO box 19615-1178, Tehran, Iran.

3. Neuroscience Research Center, Shahid Beheshti University of Medical Sciences, PO box 19615-1178, Tehran, Iran.

4. Department of Sport Physiology, Faculty of Physical Education and Sport Sciences, Shahid Beheshti University, PO box 19839-6113, Tehran, Iran.

5. Department of Physiology, Faculty of Medicine, Tehran University of Medical Sciences, PO box 141761-3151, Tehran, Iran.

Abstract

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.

Publisher

Canadian Science Publishing

Subject

Physiology (medical),Nutrition and Dietetics,Physiology,General Medicine,Endocrinology, Diabetes and Metabolism

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