Sazzad Nasim, Fahad Fowzul Islam, Sakib Shahenur Alam, Tayab Mohammed Abu, Hanif Md Abu, Reza A S M Ali, Islam Mohammad Nazmul, Capasso Raffaele
Department of Pharmacy, International Islamic University Chittagong, Chittagong, 4318, Bangladesh.
Department of Pharmacy, Jahangirnagar University, Savar, Dhaka 1342, Bangladesh.
Heliyon. 2024 Sep 26;10(19):e38541. doi: 10.1016/j.heliyon.2024.e38541. eCollection 2024 Oct 15.
is a common tropical seacoast flowering plant from the family of Fabaceae which is reported as bay bean and coastal jack bean; has a wide range of therapeutic and nutraceutical properties.
The present research aims to explore some pharmacological insights of the methanol extract of leaves (MECR) and its chloroform fraction (CFCR) and n-hexane fraction (NFCR) through and approaches.
Different fractions of were subjected to ferric reduction assay and total phenolic and flavonoid content assay to explore their antioxidant potential. The anti-inflammatory activity was assessed on the hypotonic-induced human erythrocyte-lysis model, while the protein denaturation method was applied for screening anti-arthritis properties of plant extract; and the cytotoxic activity was evaluated by brine shrimp lethality bioassay. In the in-silico study, molecular docking, pass prediction and ADME/T, analysis was used to investigate anti-arthritic, anti-inflammatory, antioxidant and cytotoxic potency of five selected compounds of . Finally, the quantum chemical density functional test analysis was applied to investigate the chemical and physical properties of those compounds.
All the soluble organic extracts of demonstrated moderate toxicity with strong antioxidants potential, in which MECR manifested the peak level of scavenging activity (2.49) on ferric reduction assay. MECR, CFCR & NFCR significantly protected lysis of human erythrocyte membrane induced by hypotonic solution, whereas MECR and CFCR were exhibited partially equal inhibitory activity. The anti-arthritis assay, MECR, NFCR and CFCR showed strongly significant (p˂0.001) inhibitory potency at 500 μg/mL & 1000 μg/mL concentrations. The molecular docking simulations revealed strong binding of all compounds to specific receptors, with Rutin showing the highest biological reactivity followed by Daucosterol, β-Sitosterol, Stigmasterol, and Guanidine. All the compounds showed favorable reactivity patterns, with O and H atoms poised for nucleophilic and electrophilic attacks in chemical density functional calculations.
The recent investigation suggests that could have the potential source of antioxidant, anti-inflammatory, anti-arthritis and cytotoxic activity prompting further investigation into their mechanisms.
是豆科常见的热带海岸开花植物,被报道为海豆和海滨刀豆;具有广泛的治疗和营养保健特性。
本研究旨在通过体外和计算机模拟方法探索叶甲醇提取物(MECR)及其氯仿馏分(CFCR)和正己烷馏分(NFCR)的一些药理见解。
对的不同馏分进行铁还原测定以及总酚和黄酮含量测定,以探索其抗氧化潜力。在低渗诱导的人红细胞裂解模型上评估抗炎活性,同时采用蛋白质变性方法筛选植物提取物的抗关节炎特性;并通过卤虫致死生物测定法评估细胞毒性活性。在计算机模拟研究中,使用分子对接、通路预测和ADME/T分析来研究的五种选定化合物的抗关节炎、抗炎、抗氧化和细胞毒性效力。最后,应用量子化学密度泛函测试分析来研究这些化合物的化学和物理性质。
的所有可溶性有机提取物均表现出中等毒性和强大的抗氧化潜力,其中MECR在铁还原测定中表现出最高的清除活性峰值(2.49)。MECR、CFCR和NFCR显著保护低渗溶液诱导的人红细胞膜裂解,而MECR和CFCR表现出部分相等的抑制活性。在抗关节炎试验中,MECR、NFCR和CFCR在500μg/mL和1000μg/mL浓度下显示出极强的抑制效力(p˂0.001)。分子对接模拟显示所有化合物与特定受体有强结合,芦丁显示出最高的生物反应性,其次是胡萝卜苷、β-谷甾醇、豆甾醇和胍。所有化合物均显示出良好的反应模式,在化学密度泛函计算中,O和H原子准备好进行亲核和亲电攻击。
最近的研究表明,可能是抗氧化、抗炎、抗关节炎和细胞毒性活性的潜在来源,促使对其作用机制进行进一步研究。