Goh Yu Xian, Jalil Juriyati, Lam Kok Wai, Husain Khairana, Premakumar Chandini Menon
Centre for Drug and Herbal Development, Faculty of Pharmacy, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.
Centre for Quality Management of Medicines, Faculty of Pharmacy, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.
Front Pharmacol. 2022 Jan 24;13:820969. doi: 10.3389/fphar.2022.820969. eCollection 2022.
Nowadays, non-resolving inflammation is becoming a major trigger in various diseases as it plays a significant role in the pathogenesis of atherosclerosis, asthma, cancer, obesity, inflammatory bowel disease, chronic obstructive pulmonary disease, neurodegenerative disease, multiple sclerosis, and rheumatoid arthritis. However, prolonged use of anti-inflammatory drugs is usually accompanied with undesirable effects and hence more patients tend to seek for natural compounds as alternative medicine. Considering the fact above, there is an urgency to discover and develop potential novel, safe and efficacious natural compounds as drug candidates for future anti-inflammatory therapy. Genistein belongs to the flavonoid family, in the subgroup of isoflavones. It is a phytoestrogen that is mainly derived from legumes. It is a naturally occurring chemical constituent with a similar chemical structure to mammalian estrogens. It is claimed to exert many beneficial effects on health, such as protection against osteoporosis, reduction in the risk of cardiovascular disease, alleviation of postmenopausal symptoms and anticancer properties. In the past, numerous and studies have been conducted to investigate the anti-inflammatory potential of genistein. Henceforth, this review aims to summarize the anti-inflammatory properties of genistein linking with the signaling pathways and mediators that are involved in the inflammatory response as well as its toxicity profile. The current outcomes are analysed to highlight the prospect as a lead compound for drug discovery. Data was collected using PubMed, ScienceDirect, SpringerLink and Scopus databases. Results showed that genistein possessed strong anti-inflammatory activities through inhibition of various signaling pathways such as nuclear factor kappa-B (NF-B), prostaglandins (PGs), inducible nitric oxide synthase (iNOS), proinflammatory cytokines and reactive oxygen species (ROS). A comprehensive assessment of the mechanism of action in anti-inflammatory effects of genistein is included. However, evidence for the pharmacological effects is still lacking. Further studies using various animal models to assess pharmacological effects such as toxicity, pharmacokinetics, pharmacodynamics, and bioavailability studies are required before clinical studies can be conducted. This review will highlight the potential use of genistein as a lead compound for future drug development as an anti-inflammatory agent.
如今,持续性炎症正成为各种疾病的主要诱因,因为它在动脉粥样硬化、哮喘、癌症、肥胖症、炎症性肠病、慢性阻塞性肺疾病、神经退行性疾病、多发性硬化症和类风湿性关节炎的发病机制中起着重要作用。然而,长期使用抗炎药物通常会伴随着不良影响,因此越来越多的患者倾向于寻找天然化合物作为替代药物。鉴于上述事实,迫切需要发现和开发潜在的新型、安全且有效的天然化合物作为未来抗炎治疗的候选药物。染料木黄酮属于黄酮类家族,是异黄酮亚组中的一员。它是一种主要来源于豆类的植物雌激素。它是一种天然存在的化学成分,其化学结构与哺乳动物雌激素相似。据称它对健康有许多有益作用,如预防骨质疏松、降低心血管疾病风险、缓解绝经后症状以及具有抗癌特性。过去,已经进行了大量研究来探究染料木黄酮的抗炎潜力。从今往后,本综述旨在总结染料木黄酮的抗炎特性,及其与炎症反应中涉及的信号通路和介质的关联以及其毒性概况。分析当前结果以突出其作为药物发现先导化合物的前景。通过使用PubMed、ScienceDirect、SpringerLink和Scopus数据库收集数据。结果表明,染料木黄酮通过抑制多种信号通路,如核因子κB(NF-κB)、前列腺素(PGs)、诱导型一氧化氮合酶(iNOS)、促炎细胞因子和活性氧(ROS),具有强大的抗炎活性。其中包括对染料木黄酮抗炎作用机制的全面评估。然而,其药理作用的证据仍然不足。在进行临床研究之前,需要使用各种动物模型进行进一步研究,以评估其毒性、药代动力学、药效学和生物利用度等药理作用。本综述将突出染料木黄酮作为未来抗炎药物开发先导化合物的潜在用途。