Mingori Moara Rodrigues, Heimfarth Luana, Ferreira Charles Francisco, Gomes Henrique Mautone, Moresco Karla Suzana, Delgado Jeferson, Roncato Sabrina, Zeidán-Chuliá Fares, Gelain Daniel Pens, Moreira José Cláudio Fonseca
Programa de Pós-Graduação em Ciências Biológicas: Bioquímica, Instituto de Ciências Básicas da Saúde (ICBS), Universidade Federal do Rio Grande do Sul (UFRGS), Rua Ramiro Barcelos 2600 Anexo, Porto Alegre, RS, 90035-000, Brazil.
Laboratório de Estresse Oxidativo, Departamento de Bioquímica, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, RS, Brazil.
Neurochem Res. 2017 Aug;42(8):2257-2273. doi: 10.1007/s11064-017-2238-4. Epub 2017 Mar 27.
During aging, there is a marked decline in the antioxidant capacity of brain tissue, leading to a gradual loss of the antioxidant/oxidant balance, which causes oxidative damage. The effects of Paullinia cupana Mart. extract, which is described as being rich in caffeine and many polyphenol compounds, on the central nervous system have not been extensively investigated. The aim of this study was to therefore investigate the effect of a commercial guarana extract (CGE) on cognitive function, oxidative stress, and brain homeostasis proteins related to cognitive injury and senescence in middle age, male Wistar rats. Animals were randomly assigned to a group according to their treatment (saline, CGE, or caffeine). Solutions were administered daily by oral gavage for 6 months. Open field and novel object recognition tasks were performed before and after treatment. Biochemical analyses were carried out on the hippocampus and striatum. Our open field data showed an increase in exploratory activity and a decrease in anxiety-like behavior with caffeine but not with the CGE treatment. In the CGE-treated group, catalase activity decreased in the hippocampus and increased in the striatum. Analyses of the hippocampus and striatum indicate that CGE and/or caffeine altered some of the analyzed parameters in a tissue-specific manner. Our data suggest that CGE intake does not improve cognitive development, but modifies the oxidative stress machinery and neurodegenerative-signaling pathway, inhibiting pro-survival pathway molecules in the hippocampus and striatum. This may contribute to the development of unfavorable microenvironments in the brain and neurodegenerative disorders.
在衰老过程中,脑组织的抗氧化能力显著下降,导致抗氧化剂/氧化剂平衡逐渐丧失,从而引起氧化损伤。巴西可可(Paullinia cupana Mart.)提取物富含咖啡因和多种多酚化合物,但其对中枢神经系统的影响尚未得到广泛研究。因此,本研究的目的是调查一种商业瓜拉那提取物(CGE)对中年雄性Wistar大鼠认知功能、氧化应激以及与认知损伤和衰老相关的脑稳态蛋白的影响。根据治疗方法(生理盐水、CGE或咖啡因)将动物随机分组。通过口服灌胃每天给药溶液,持续6个月。在治疗前后进行旷场试验和新物体识别任务。对海马体和纹状体进行生化分析。我们的旷场试验数据显示,咖啡因可增加探索活动并减少焦虑样行为,但CGE治疗则无此效果。在CGE治疗组中,海马体中的过氧化氢酶活性降低,而纹状体中的过氧化氢酶活性增加。对海马体和纹状体的分析表明,CGE和/或咖啡因以组织特异性方式改变了一些分析参数。我们的数据表明,摄入CGE并不能改善认知发育,但会改变氧化应激机制和神经退行性信号通路,抑制海马体和纹状体中的促生存通路分子。这可能有助于大脑中不利微环境的形成和神经退行性疾病的发展。