Ovarian and Prostate Cancer Research Trust Laboratory, University of Surrey Technology Centre, 10 Nugent Road, Guildford, Surrey, UK.
Curr Drug Targets. 2011 Mar 1;12(3):288-301. doi: 10.2174/138945011794815347.
Inflammation is a natural response of living organisms to the presence of internal and external substances which are recognized by the host as being "non-self" or "foreign invader". It is also a cascade leading to the healing of damaged tissue. Uncontrolled inflammation often results in chronic diseases such as arthritis, autoimmune disorder, cancer, dementia, diabetic, neurodegeneration and vascular disease. The list keeps growing due to the increasing numbers of identified molecular markers that are associated with inflammatory genes or transcription factors. Among various transcription factors, nuclear factor kappa B (NF-kB) is the master switch for proinflammatory genes and transactivates arachidonic acid pathway enzymes when activated. Through evolution, plants have developed vast classes of compounds to fight inflammation. Most of them belong to the chemical group of alkaloids, coumarins, flavonoids, polyphenols and terpenoids. This review article presents and discusses results obtained from literature search on recent findings in plant-derived compounds, which exhibit anti-inflammatory activity in rheumatoid arthritis, allergy and asthma via the suppression of the arachidonic acid pathway. IC(50)s of the compounds obtained from the literature are thus tabulated into six groups of inhibitors based on the enzyme target of phospholipase A2, cyclooxygenase 1 and 2, 5-, 12- and 15-lipoxygenase. Modulation of Th1/Th2 cytokines and histamine/mucus release by some of these enzyme inhibitors are also briefly discussed.
炎症是生物体对被宿主识别为“非自身”或“外来入侵者”的内外部物质的自然反应。它也是导致受损组织愈合的级联反应。失控的炎症通常会导致关节炎、自身免疫性疾病、癌症、痴呆、糖尿病、神经退行性疾病和血管疾病等慢性疾病。由于与炎症基因或转录因子相关的鉴定分子标志物数量不断增加,这个清单还在不断增加。在各种转录因子中,核因子 kappa B(NF-kB)是促炎基因的主开关,当被激活时,它会转激活花生四烯酸途径的酶。植物通过进化产生了大量的化合物来对抗炎症。它们中的大多数属于生物碱、香豆素、类黄酮、多酚和萜类化合物等化学基团。本文综述了植物源性化合物在类风湿关节炎、过敏和哮喘中的抗炎活性的最新研究结果,这些结果通过抑制花生四烯酸途径来展示。因此,根据文献中获得的化合物对磷脂酶 A2、环加氧酶 1 和 2、5-、12-和 15-脂氧合酶的酶靶标,将 IC50 值列成了六组抑制剂。还简要讨论了其中一些酶抑制剂对 Th1/Th2 细胞因子和组胺/黏液释放的调节作用。