| dc.description.abstract | Omrani, Hasan, Mohammad Reza Alipour, Fereshteh Farajdokht, Hadi Ebrahimi, Mehran Mesgari Abbasi, and Gisou Mohaddes. Effects of chronic ghrelin treatment on hypoxia-induced brain oxidative stress and inflammation in a rat normobaric chronic hypoxia model. High Alt Med Biol. 18:145-151, 2017. Aim: This study aimed to evaluate the probable antioxidant effects of ghrelin in the brain and serum and its effect on tumor necrosis factor-alpha (TNF-) levels in the brain in a model of chronic systemic hypoxia in rats. Methods: Systemic hypoxia was induced by a normobaric hypoxic chamber (O-2 11%) for ten days. Adult male Wistar rats were divided into control (C), chronic ghrelin (80g/kg/10 days) (Ghr), chronic hypoxia (CH), and CH and ghrelin (80g/kg/ip/10 days) (CH + Gh) groups. The activity of superoxide dismutase (SOD), glutathione peroxidase (GPx), catalase (CAT), and malondialdehyde (MDA), total antioxidant capacity, and TNF- levels were assessed in the serum and brain tissue. Results: Our results showed that chronic ghrelin administration attenuated the CH-increased oxidative stress by decreasing MDA levels in the serum and brain tissue. Moreover, ghrelin enhanced the antioxidant defense against hypoxia-induced oxidative stress in the serum and brain tissue. Brain TNF- levels in CH did not change significantly; however, ghrelin significantly (p<0.001) decreased it. Conclusion: These results indicated that ghrelin promoted antioxidative and anti-inflammatory defense under chronic exposure to hypoxia. Therefore, ghrelin might be used as a potential therapy in normobaric hypoxia and oxidative stress induced by CH. | |
