Pharmacy Discipline, Life Science School, Khulna University, Khulna, Bangladesh.
Department of Pharmacy, Faculty of Life Science, Bangabandhu Sheikh Mujibur Rahman Science & Technology University, Gopalganj, Bangladesh.
Phytother Res. 2019 Oct;33(10):2585-2608. doi: 10.1002/ptr.6428. Epub 2019 Aug 1.
Traditionally, sesame oil (SO) has been used as a popular food and medicine. The review aims to summarize the antioxidant and antiinflammatory effects of SO and its identified compounds as well as further fatty acid profiling and molecular docking study to correlate the interaction of its identified constituents with cyclooxygenase-2 (COX-2). For this, a literature study was made using Google Scholar, Pubmed, and SciFinder databases. Literature study demonstrated that SO has potential antioxidant and antiinflammatory effects in various test systems, including humans, animals, and cultured cells through various pathways such as inhibition of COX, nonenzymatic defense mechanism, inhibition of proinflammatory cytokines, NF-kB or mitogen-activated protein kinase signaling, and prostaglandin synthesis pathway. Fatty acid analysis of SO using gas chromatography identified known nine fatty acids. In silico study revealed that sesamin, sesaminol, sesamolin, stigmasterol, Δ5-avenasterol, and Δ7-avenasterol (-9.6 to -10.7 kcal/mol) were the most efficient ligand for interaction and binding with COX-2. The known fatty acid also showed binding efficiency with COX-2 to some extent (-6.0 to -8.4 kcal/mol). In summary, it is evident that SO may be one of promising traditional medicines that we could use in the prevention and management of diseases associated with oxidative stress and inflammation.
传统上,芝麻油(SO)一直被用作流行的食品和药物。本综述旨在总结 SO 及其鉴定化合物的抗氧化和抗炎作用,以及进一步的脂肪酸分析和分子对接研究,以关联其鉴定成分与环氧化酶-2(COX-2)的相互作用。为此,使用 Google Scholar、Pubmed 和 SciFinder 数据库进行了文献研究。文献研究表明,SO 通过抑制 COX、非酶防御机制、抑制促炎细胞因子、NF-κB 或丝裂原活化蛋白激酶信号通路以及前列腺素合成途径等各种途径,在各种测试系统中具有潜在的抗氧化和抗炎作用,包括人类、动物和培养细胞。使用气相色谱法对 SO 的脂肪酸分析鉴定出已知的 9 种脂肪酸。计算机模拟研究表明,芝麻素、芝麻林酚、芝麻脂素、豆甾醇、Δ5-菜油甾醇和Δ7-菜油甾醇(-9.6 至-10.7 kcal/mol)是与 COX-2 相互作用和结合的最有效配体。已知的脂肪酸也在一定程度上显示出与 COX-2 的结合效率(-6.0 至-8.4 kcal/mol)。综上所述,很明显,SO 可能是我们可以在预防和管理与氧化应激和炎症相关的疾病中使用的有前途的传统药物之一。