da Silva Schmitz Izaviany, Schaffer Larissa Finger, Busanello Alcindo, de Freitas Catiuscia Molz, Fachinetto Roselei, Peroza Luis Ricardo
Curso de Biomedicina, Universidade Franciscana (UFN), Santa Maria, Rio Grande do Sul, Brazil.
Programa de Pós-Graduação em Farmacologia, Universidade Federal de Santa Maria (UFSM), Santa Maria, Rio Grande do Sul, Brazil.
Mol Biol Rep. 2019 Apr;46(2):2285-2292. doi: 10.1007/s11033-019-04684-z. Epub 2019 Feb 12.
Oxidative stress occurs due to an imbalance between antioxidant defenses and pro-oxidant agents in brain. This condition has been associated to the pathogenesis of several brain diseases; therefore, increasing the use of compounds that exert antioxidant activity. Thus, the objective of this study was to evaluate, in vitro, the effect of isoflavones in: (1) lipid peroxidation, catalase activity and thiol groups in the presence of pro-oxidants: sodium nitroprusside or Fe/EDTA complex in rat brain homogenates; (2) the activity of the enzyme monoamine oxidase (MAO). As a result, the isoflavones reduced lipid peroxidation in a manner dependent on the concentration and protected against the reduction of catalase activity as well as the induced thiol oxidation in brain tissue. In addition, isoflavones inhibited MAO activity (MAO-A and MAO-B). Taken together, our results showed that isoflavones avoided oxidative stress and decreased the MAO activity, suggesting a promissory use in the treatment of neurodegenerative diseases.
氧化应激是由于大脑中抗氧化防御系统与促氧化剂之间的失衡而发生的。这种情况与几种脑部疾病的发病机制有关;因此,具有抗氧化活性的化合物的使用日益增加。因此,本研究的目的是在体外评估异黄酮在以下方面的作用:(1)在存在促氧化剂(硝普钠或铁/乙二胺四乙酸复合物)的情况下,大鼠脑匀浆中的脂质过氧化、过氧化氢酶活性和巯基;(2)单胺氧化酶(MAO)的活性。结果,异黄酮以浓度依赖性方式减少脂质过氧化,并防止脑组织中过氧化氢酶活性的降低以及诱导的巯基氧化。此外,异黄酮抑制MAO活性(MAO-A和MAO-B)。综上所述,我们的结果表明异黄酮可避免氧化应激并降低MAO活性,提示其在神经退行性疾病治疗中具有潜在应用价值。