Francolino Rosaria, Martino Mara, Caputo Lucia, Amato Giuseppe, Chianese Giuseppina, Gargiulo Ernesto, Formisano Carmen, Romano Benedetta, Ercolano Giuseppe, Ianaro Angela, De Martino Laura, Feo Vincenzo De
Department of Pharmacy, University of Salerno, Via Giovanni Paolo II, 132, 84084 Fisciano, Italy.
Department of Pharmacy, School of Medicine and Surgery, University of Napoli Federico II, Via D. Montesano, 49, 80131 Napoli, Italy.
Antioxidants (Basel). 2023 Aug 18;12(8):1633. doi: 10.3390/antiox12081633.
L. is an aromatic evergreen plant from the Lamiaceae family. The purpose of this study was to compare the chemical profile and bioactivities of hydroalcoholic extracts derived from wild and cultivated . The chemical composition of the extracts was evaluated via LC-MS analysis, which revealed the presence of a wide range of phenolic compounds, including flavonoids, phenolic and terpenes. Both extracts showed a similar interesting antioxidant activity, probably related to their content of phenol and flavonoids. The analysis of anti-acetylcholinesterase (AChE), anti-butyrylcholinesterase (BChE), and anti-α-amylase activities showed analogous inhibition, except for AChE, in which the wild type was more active than the cultivated one. Finally, in vitro studies were performed using the J774A.1 murine macrophage cell line, to characterize the anti-inflammatory and the antioxidant effects of the extracts. As expected, pretreatment with the extracts significantly reduced the production proinflammatory cytokines and ROS through modulation of the nitric oxide pathway and the mitochondrial activity. Importantly, it is observed that the anti-inflammatory effect of the extracts was explicated through the inhibition of NF-kB and its downstream mediator COX-2. Collectively, these results demonstrated that these extracts could represent a starting point for developing novel therapeutic strategies for the treatment of inflammation-based diseases. Moreover, since no significant changes were observed in terms of composition and activity, both wild and cultivated extracts can be recommended for food and pharmaceutical purposes.
罗勒是一种唇形科的芳香常绿植物。本研究的目的是比较野生和栽培罗勒水醇提取物的化学特征和生物活性。通过液相色谱 - 质谱分析评估提取物的化学成分,结果显示存在多种酚类化合物,包括黄酮类、酚类和萜类。两种提取物均表现出相似的有趣抗氧化活性,这可能与其酚类和黄酮类含量有关。抗乙酰胆碱酯酶(AChE)、抗丁酰胆碱酯酶(BChE)和抗α -淀粉酶活性分析显示出类似的抑制作用,但AChE除外,其中野生型比栽培型更具活性。最后,使用J774A.1小鼠巨噬细胞系进行体外研究,以表征提取物的抗炎和抗氧化作用。正如预期的那样,提取物预处理通过调节一氧化氮途径和线粒体活性显著降低了促炎细胞因子和活性氧的产生。重要的是,观察到提取物的抗炎作用是通过抑制核因子κB及其下游介质环氧化酶 - 2来实现的。总体而言,这些结果表明这些提取物可能是开发基于炎症性疾病治疗的新型治疗策略的起点。此外,由于在成分和活性方面未观察到显著变化,野生和栽培罗勒提取物均可推荐用于食品和制药目的。