Elmaidomy Abeer H, Abdelmohsen Usama Ramadan, Alsenani Faisal, Aly Hanan F, Eldin Shams Shams Gamal, Younis Eman A, Ahmed Kawkab A, Sayed Ahmed M, Owis Asmaa I, Afifi Naglaa, El Amir Dalia
Department of Pharmacognosy, Faculty of Pharmacy, Beni-Suef University Beni-Suef 62514 Egypt.
Department of Pharmacognosy, Faculty of Pharmacy, Minia University Minia 61519 Egypt
RSC Adv. 2022 Apr 19;12(19):11769-11785. doi: 10.1039/d2ra01340a. eCollection 2022 Apr 13.
Linn. (Tamarind, F. Fabaceae) is one of the most widely consumed fruits in the world. A crude extract and different fractions of (using -hexane, dichloromethane, ethyl acetate, and -butanol) were evaluated with respect to their DPPH scavenging and AchE inhibition activities. The results showed that the dichloromethane and ethyl acetate fractions showed the highest antioxidant activities, with 84.78 and 86.96% DPPH scavenging at 0.10 μg mL. The -hexane, dichloromethane, and ethyl acetate fractions inhibited AchE activity in a dose-dependent manner, and the -hexane fraction showed the highest inhibition at 20 μg mL. The results were confirmed by using -hexane, dichloromethane, and ethyl acetate fractions to regress the neurodegenerative features of Alzheimer's dementia in an aluminum-intoxicated rat model. Phytochemical investigations of those three fractions afforded two new diphenyl ether derivative compounds 1-2, along with five known ones (3-7). The structures of the isolated compounds were confirmed 1D and 2D NMR and HRESIMS analyses. The isolated compounds were subjected to extensive -based investigations to putatively highlight the most probable compounds responsible for the anti-Alzheimer activity of . Inverse docking studies followed by molecular dynamics simulation (MDS) and binding free energy (Δ) investigations suggested that both compounds 1 and 2 could be promising AchE inhibitors. The results presented in this study may provide potential dietary supplements for the management of Alzheimer's disease.
罗望子(罗望子,豆科)是世界上消费最为广泛的水果之一。对罗望子的粗提物以及不同萃取部位(使用正己烷、二氯甲烷、乙酸乙酯和正丁醇)进行了二苯基苦味酰基自由基(DPPH)清除能力和乙酰胆碱酯酶(AchE)抑制活性的评估。结果表明,二氯甲烷和乙酸乙酯部位表现出最高的抗氧化活性,在0.10μg/mL时DPPH清除率分别为84.78%和86.96%。正己烷、二氯甲烷和乙酸乙酯部位均以剂量依赖方式抑制AchE活性,正己烷部位在20μg/mL时表现出最高抑制率。通过使用正己烷、二氯甲烷和乙酸乙酯部位对铝中毒大鼠模型中阿尔茨海默病的神经退行性特征进行回归分析,证实了上述结果。对这三个部位进行植物化学研究,得到了两种新的二苯醚衍生物化合物1 - 2,以及五种已知化合物(3 - 7)。通过一维和二维核磁共振以及高分辨电喷雾电离质谱分析确定了分离得到化合物的结构。对分离得到的化合物进行了广泛的基于配体的研究,以推测出最有可能是罗望子抗阿尔茨海默病活性原因的化合物。反向对接研究,随后进行分子动力学模拟(MDS)和结合自由能(Δ)研究表明,化合物1和2都可能是有前景的AchE抑制剂。本研究所得结果可能为阿尔茨海默病的管理提供潜在的膳食补充剂。