Anukanon Shisanupong, Saeng-Ngoen Komgrit, Ngamnon Yawanart, Rapan Ngamnetr, Seelarat Weerasak, Takolpuckdee Pannraphat, Pakvilai Nisa, Chatree Yaiprae
School of Medicine, Mae Fah Luang University, Chiang Rai 57100, Thailand.
Cancer and Immunology Research Unit (CIRU), School of Medicine, Mae Fah Luang University, Chiang Rai 57100, Thailand.
Food Chem (Oxf). 2025 Aug 25;11:100291. doi: 10.1016/j.fochms.2025.100291. eCollection 2025 Dec.
Curcuminoids are the active compounds richest in turmeric rhizomes ( L.), comprising curcumin I, demethoxycurcumin (curcumin II), and bisdemethoxycurcumin (curcumin III). This study hypothesized that particular curcumin derivatives could mitigate oxidative stress and inflammation response by targeting specific inflammatory mediators. Therefore, this study aimed to quantify the concentrations of these curcuminoid forms in local turmeric extracts from Thailand. Subsequently, the study analyzed their antioxidant properties, alongside molecular docking and dynamics simulations targeting key oxidative stress- and inflammation-related proteins. Samples were collected from three representative cultivated areas in Thailand: the eastern, southern, and northern regions. The ethanolic extracts from all samples exhibited relatively high total curcuminoid content (eastern: 15.1 %, southern: 25.9 %, and northern: 31.6 % /w in extract), as determined by high-performance liquid chromatography. Curcumin I emerged as the predominant variant, followed closely by curcumin II and III. The ethanolic extracts from the three cultural areas demonstrated significant antioxidant activity, as assessed by ORAC, FRAP, and DPPH assays. Among the three curcuminoids, curcumin III exhibited the strongest predicted binding affinities in molecular docking studies toward antioxidant and anti-inflammatory targets, including 5-LOX, NRF2, IKK1, NF-κB, and NOX4. Molecular dynamics simulations corroborated these findings, revealing that curcumin III formed the most stable complexes, particularly with IKK1, as indicated by low RMSD values (2-3 Å), and high hydrogen bond occupancy. Thus, curcumin III exhibits potential inhibition of inflammatory mediators, supporting its promise as a natural compound for antioxidant and anti-inflammatory nutraceutical development.
姜黄素类化合物是姜黄根茎(姜黄)中含量最丰富的活性化合物,包括姜黄素 I、去甲氧基姜黄素(姜黄素 II)和双去甲氧基姜黄素(姜黄素 III)。本研究假设特定的姜黄素衍生物可通过靶向特定炎症介质来减轻氧化应激和炎症反应。因此,本研究旨在量化泰国当地姜黄提取物中这些姜黄素类化合物的浓度。随后,该研究分析了它们的抗氧化特性,以及针对关键氧化应激和炎症相关蛋白的分子对接和动力学模拟。样本采集自泰国三个具有代表性的种植区:东部、南部和北部地区。通过高效液相色谱法测定,所有样本的乙醇提取物均显示出相对较高的总姜黄素类化合物含量(东部:提取物中为15.1%,南部:25.9%,北部:31.6% /w)。姜黄素 I 是主要变体,其次是姜黄素 II 和 III。通过ORAC、FRAP和DPPH测定评估,这三个种植区的乙醇提取物均表现出显著的抗氧化活性。在这三种姜黄素类化合物中,姜黄素 III 在分子对接研究中对包括5-LOX、NRF2、IKK1、NF-κB和NOX4在内的抗氧化和抗炎靶点表现出最强的预测结合亲和力。分子动力学模拟证实了这些发现,表明姜黄素 III 形成了最稳定的复合物,特别是与IKK1形成的复合物,低RMSD值(2 - 3 Å)和高氢键占有率表明了这一点。因此,姜黄素 III 具有潜在的抑制炎症介质的作用,支持其作为抗氧化和抗炎营养保健品开发的天然化合物的前景。