Department of Chemistry, Vassar College, Poughkeepsie, NY 12604, USA.
Facultad de Farmacia y Bioquímica, Universidad Nacional San Luis Gonzaga, Ica 11004, Peru.
Int J Mol Sci. 2023 Jun 28;24(13):10750. doi: 10.3390/ijms241310750.
The relationship between oxidative stress and inflammation is well known, and exogenous antioxidants, primarily phytochemical natural products, may assist the body's endogenous defense systems in preventing diseases due to excessive inflammation. In this study, we evaluated the antioxidant properties of ethnomedicines from Peru that exhibit anti-inflammatory activity by measuring the superoxide scavenging activity of ethanol extracts of aerial parts using hydrodynamic voltammetry at a rotating ring-disk electrode (RRDE). The chemical compositions of these extracts are known and the interactions of three methide-quinone compounds found in with caspase-1 were analyzed using computational docking studies. Caspase-1 is a critical enzyme triggered during the activation of the inflammasome and its actions are associated with excessive release of cytokines. The most important amino acid involved in active site caspase-1 inhibition is Arg341 and, through docking calculations, we see that this amino acid is stabilized by interactions with the three potential methide-quinone inhibitors, hydroxytingenone, tingenone, and pristimerin. These findings were also confirmed after more rigorous molecular dynamics calculations. It is worth noting that, in these three compounds, the methide-quinone carbonyl oxygen is the preferred hydrogen bond acceptor site, although tingenone's other carbonyl group also shows a similar binding energy preference. The results of these calculations and cyclovoltammetry studies support the effectiveness and use of anti-inflammatory ethnopharmacological ethanol extract of (L'Héritier) DC.
氧化应激和炎症之间的关系是众所周知的,外源性抗氧化剂,主要是植物化学天然产物,可能有助于身体的内源性防御系统预防因过度炎症而导致的疾病。在这项研究中,我们评估了具有抗炎活性的秘鲁民族医学的抗氧化特性,方法是使用旋转环盘电极(RRDE)在流体动力学伏安法下测量空中部分乙醇提取物对超氧化物的清除活性。这些提取物的化学成分是已知的,并且使用计算对接研究分析了在与半胱天冬酶-1相互作用的三种甲酰醌化合物。半胱天冬酶-1是在炎症小体激活过程中触发的关键酶,其作用与细胞因子的过度释放有关。在活性位点半胱天冬酶-1抑制中涉及的最重要的氨基酸是 Arg341,并且通过对接计算,我们看到该氨基酸通过与三个潜在的甲酰醌抑制剂羟基续随子醌、续随子醌和普瑞司他汀的相互作用而稳定。在更严格的分子动力学计算之后,也证实了这些发现。值得注意的是,在这三种化合物中,甲酰醌羰基氧是首选的氢键接受位点,尽管续随子醌的另一个羰基也表现出类似的结合能偏好。这些计算和循环伏安法研究的结果支持抗炎民族药理学乙醇提取物的有效性和使用(L'Héritier)DC。