Research Unit of Macromolecular Biochemistry and Genetics, Faculty of Sciences of Gafsa, 2112, Gafsa, Tunisia.
Laboratoire d'Ecologie, de Biologie et de Physiologie des Organismes Aquatiques, LR18ES41, Faculté des Sciences de Tunis, Université Tunis EL Manar, 2092, Tunis, Tunisia.
Inflammopharmacology. 2021 Apr;29(2):467-481. doi: 10.1007/s10787-021-00791-1. Epub 2021 Feb 26.
The aim of the current work was to study the phytochemical variability among Schinus terebinthifolius (STE) and Schinus molle (SME) fruit extracts. The in vitro antioxidant, antihemolytic, antidiabetic, and macromolecule damage protective activities, as well as, the in vivo anti-inflammatory and antinociceptive capacities were assessed. Using the HPLC-ESI-QTOF/MS analysis, the chemical profile of fruit extract varied between S. terebinthifolius (30 compounds) and S. molle (16 compounds). The major compound was masazino-flavanone (5774.98 and 1177.65 μg/g sample for STE and SME, respectively). The investigations highlighted significant antioxidant proprieties when using ABTS radical (IC; 0.12 and 0.14 mg/ml for STE and SME, respectively), superoxide (IC; 0.17 and 0.22 mg/ml for STE and SME, respectively) and hydrogen peroxide (IC; 014 and 0.17 mg/ml for STE and SME, respectively). In addition, STE and SME proved preventive effects against HO-induced hemolysis (IC; 0.22 and 0.14 mg/ml for STE and SME, respectively). The in vitro antidiabetic effect revealed that STE and SME exhibited important inhibitory effects against α-amylase (IC; 0.13 and 0.19 mg/ml for STE and SME, respectively) and α-glycosidase (IC; 0.21 and 0.18 mg/ml for STE and SME, respectively) when compared with acarbose. Furthermore, the extracts showed potent inhibitory activity against AAPH-induced plasmid DNA damage, and protein oxidation. In vivo study revealed that STE and SME presented interesting antinociceptive and anti-inflammatory capacities. All observed effects highlighted the potential application of Schinus fruit extract in food and pharmaceutical industries against ROS-induced damage.
本研究旨在研究灌丛山榄(STE)和软毛山榄(SME)果实提取物的植物化学成分变化。评估了其体外抗氧化、抗溶血、抗糖尿病、大分子损伤保护活性,以及体内抗炎和镇痛作用。通过 HPLC-ESI-QTOF/MS 分析,果实提取物的化学成分在 STE(30 种化合物)和 SME(16 种化合物)之间存在差异。主要化合物为马萨佐诺黄酮(STE 和 SME 中分别为 5774.98 和 1177.65μg/g 样品)。研究结果表明,STE 和 SME 在使用 ABTS 自由基(IC;STE 和 SME 分别为 0.12 和 0.14mg/ml)、超氧自由基(IC;STE 和 SME 分别为 0.17 和 0.22mg/ml)和过氧化氢(IC;STE 和 SME 分别为 0.14 和 0.17mg/ml)时具有显著的抗氧化性能。此外,STE 和 SME 对 HO 诱导的溶血具有预防作用(IC;STE 和 SME 分别为 0.22 和 0.14mg/ml)。体外抗糖尿病作用表明,与阿卡波糖相比,STE 和 SME 对α-淀粉酶(IC;STE 和 SME 分别为 0.13 和 0.19mg/ml)和α-糖苷酶(IC;STE 和 SME 分别为 0.21 和 0.18mg/ml)具有重要的抑制作用。此外,提取物对 AAPH 诱导的质粒 DNA 损伤和蛋白质氧化具有较强的抑制活性。体内研究表明,STE 和 SME 具有较好的镇痛和抗炎作用。所有观察到的作用都强调了灌丛山榄果实提取物在食品和制药工业中对抗 ROS 诱导损伤的潜在应用。