Antiinflammatory efficacy of n-Hexadecanoic acid from a mangrove plant Excoecaria agallocha L. through in silico, in vitro and in vivo

Ramamoorthy Purushothaman, Ganapathy Vishnuram, Thirugnanasambandam Ramanathan
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Abstract

The various parts of Excoecaria agallocha L. have been scientifically evaluated for their role in inflammatory reactions. This study aimed to validate the potent anti-inflammatory efficacy of n-Hexadecanoic acid (HDA) isolated from Excoecaria agallocha using in silico, in vitro, and in vivo approaches. GC-MS and NMR analyses were employed for compound identification, revealing 30 phytochemical constituents. Molecular docking studies demonstrated strong inhibitory interactions between HDA and key inflammatory mediators, cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2). In vitro, assays confirmed a dose-dependent anti-inflammatory response, including protein denaturation, hypotonicity-induced hemolysis, and heat-induced hemolysis tests. Furthermore, in vivo evaluation using a carrageenan-induced Wistar rat model showed significant attenuation of paw edema in HDA-treated groups compared to the control. These findings collectively establish the potent anti-inflammatory properties of n-Hexadecanoic acid and its potential as a therapeutic candidate for inflammation-related disorders.
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红树植物刺槐正十六酸在体内、体外和硅体内的抗炎作用
沉香露的各个部分在炎症反应中的作用已被科学地评估。本研究旨在通过硅片、体外和体内实验验证从沉香表皮菌中分离的正十六酸(HDA)的有效抗炎作用。采用GC-MS和NMR对化合物进行鉴定,共鉴定出30种植物化学成分。分子对接研究表明,HDA与关键炎症介质环氧化酶-1 (COX-1)和环氧化酶-2 (COX-2)具有较强的抑制相互作用。体外实验证实了剂量依赖性抗炎反应,包括蛋白变性、低张力诱导溶血和热诱导溶血试验。此外,使用卡拉胶诱导的Wistar大鼠模型进行的体内评估显示,与对照组相比,hda治疗组的足部水肿明显减轻。这些发现共同确立了正十六酸的有效抗炎特性及其作为炎症相关疾病治疗候选药物的潜力。
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