Rauf Abdur, Ibrahim Muhammad, Alomar Taghrid S, AlMasoud Najla, Khalil Anees Ahmed, Khan Muneeb, Khalid Ahood, Jan Muhammad Saeed, Formanowicz Dorota, Quradha Mohammed Mansour
Department of Chemistry University of Swabi Swabi, Anbar Khyber Pakhtunkhwa Pakistan.
Department of Chemistry, College of Science Princess Nourah bint Abdulrahman University Riyadh Saudi Arabia.
Food Sci Nutr. 2024 Feb 13;12(5):3483-3491. doi: 10.1002/fsn3.4017. eCollection 2024 May.
L., also known as babul, belonging to the Fabaceae family and the genus, is typically used for ornamental purposes and also as a medicinal plant found in tropical and subtropical areas. This plant is a rich source of bioactive compounds. The current study aimed to elucidate the hypoglycemic, anti-inflammatory, and neuroprotective potential of 's crude methanolic extract. The results of the in vitro antidiabetic assay revealed that methanolic extract of inhibited the enzyme α-glucosidase (IC: 33 μg mL) and α-amylase (IC: 17 μg mL) in a dose-dependent manner. While in the anticholinesterase enzyme inhibitory assay, maximum inhibition was shown by the extract against acetylcholinesterase (AChE) (637.01 μg mL) and butyrylcholinesterase (BChE) (491.98 μg mL), with the highest percent inhibition of 67.54% and 71.50% at 1000 μg mL, respectively. This inhibitory potential was lower as compared to the standard drug Galantamine that exhibited 82.43 and 89.50% inhibition at the same concentration, respectively. Moreover, the methanolic extract of also significantly inhibited the activities of cyclooxygenase 2 (COX-2) and 5-lipoxygenase (5-LOX) in a concentration-dependent manner. The percent inhibitory activity of 5-LOX and COX-2 ranged from 42.47% to 71.53% and 43.48% to 75.22%, respectively. Furthermore, in silico, in vivo, and clinical investigations must be planned to validate the above-stated bioactivities of .
L.,也被称为儿茶树,属于豆科和儿茶属,通常用于观赏,也是一种在热带和亚热带地区发现的药用植物。这种植物富含生物活性化合物。当前的研究旨在阐明L.的粗甲醇提取物的降血糖、抗炎和神经保护潜力。体外抗糖尿病试验的结果表明,L.的甲醇提取物以剂量依赖的方式抑制α-葡萄糖苷酶(IC:33μg/mL)和α-淀粉酶(IC:17μg/mL)。而在抗胆碱酯酶抑制试验中,该提取物对乙酰胆碱酯酶(AChE)(637.01μg/mL)和丁酰胆碱酯酶(BChE)(491.98μg/mL)表现出最大抑制作用,在1000μg/mL时最高抑制率分别为67.54%和71.50%。与标准药物加兰他敏相比,这种抑制潜力较低,加兰他敏在相同浓度下分别表现出82.43%和89.50%的抑制率。此外,L.的甲醇提取物还以浓度依赖的方式显著抑制环氧化酶2(COX-2)和5-脂氧合酶(5-LOX)的活性。5-LOX和COX-2的抑制活性百分比分别为42.47%至71.53%和43.48%至75.22%。此外,必须计划进行计算机模拟、体内和临床研究,以验证L.的上述生物活性。