Le Duc Dat, Jang Young Su, Truong Vinhquang, Yu Soojung, Dinh Thientam, Lee Mina
College of Pharmacy and Research Institute of Life and Pharmaceutical Sciences, Sunchon National University, 255 Jungangno, Suncheon 57922, Jeonnam, Republic of Korea.
Nano Bio Research Center, Jeonnam Bio Foundation, Jangseong 57248, Jeonnam, Republic of Korea.
Antioxidants (Basel). 2024 Oct 14;13(10):1235. doi: 10.3390/antiox13101235.
Acyl-quinic acids (AQAs), present in various plants with many health benefits, are regarded as therapeutic agents in the prevention and treatment of chronic and cardiovascular diseases. The molecular network-guided identification of ten AQA compounds, two new ( and ) and eight known compounds, were isolated from L. f. by using a newly applied extraction method. Their structures were determined through spectroscopic means, reaction mixtures, and modified Mosher and PGME techniques. These compounds were assessed for their anti-inflammatory and antioxidant capabilities. Notably, compounds , , , , , and exhibited notable DPPH radical scavenging activity. In LPS-induced HT-29 cells, compounds - significantly inhibited IL-8 production. Furthermore, compounds - and markedly suppressed NO production, while compounds - effectively inhibited IL-6 production in LPS-induced RAW264.7 cells. Western blot analyses revealed that compounds -, and reduced iNOS and COX-2 expression, and compounds -, , and also diminished the expression levels of p38 MAPK phosphorylation. Docking studies demonstrated the active compounds' binding affinity with the IL-8, iNOS, COX-2, and p38 MAPK proteins through interactions with essential amino acids within the binding pockets of complexes. The findings suggest that compounds , , , , , and , and compounds -, and , hold promise as potential therapeutic agents for treating antioxidative and inflammatory diseases, respectively.
酰基奎宁酸(AQAs)存在于多种植物中,具有诸多健康益处,被视为预防和治疗慢性疾病及心血管疾病的治疗剂。通过一种新应用的提取方法,从光果甘草中分离出了在分子网络引导下鉴定出的10种AQAs化合物,其中2种为新化合物(和),8种为已知化合物。通过光谱手段、反应混合物以及改良的莫舍尔和PGME技术确定了它们的结构。对这些化合物的抗炎和抗氧化能力进行了评估。值得注意的是,化合物、、、、、表现出显著的DPPH自由基清除活性。在脂多糖诱导的HT - 29细胞中,化合物 - 显著抑制白细胞介素 - 8(IL - 8)的产生。此外,化合物 - 和显著抑制一氧化氮(NO)的产生,而化合物 - 在脂多糖诱导的RAW264.7细胞中有效抑制白细胞介素 - 6(IL - 6)的产生。蛋白质免疫印迹分析表明,化合物 - 、和降低了诱导型一氧化氮合酶(iNOS)和环氧化酶 - 2(COX - 2)的表达,化合物 - 、、和也降低了p38丝裂原活化蛋白激酶(p38 MAPK)磷酸化的表达水平。对接研究表明,活性化合物通过与复合物结合口袋内的必需氨基酸相互作用,与IL - 8、iNOS、COX - 2和p38 MAPK蛋白具有结合亲和力。研究结果表明,化合物、、、、、和,以及化合物 - 、和,分别有望成为治疗抗氧化和炎症性疾病的潜在治疗剂。