Department of Pharmaceutical Chemistry, School of Pharmacy, Faculty of Health Sciences, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.
Int J Mol Sci. 2020 Mar 13;21(6):1975. doi: 10.3390/ijms21061975.
Worldwide, Alzheimer's disease (AD) is the most common neurodegenerative multifactorial disease influencing the elderly population. Nowadays, several medications, among them curcumin, are used in the treatment of AD. Curcumin, which is the principal component of , has shown favorable effects forsignificantly preventing or treating AD. During the last decade, the scientific community has focused their research on the optimization of therapeutic properties and on the improvement of pharmacokinetic properties of curcumin. This review summarizes bibliographical data from 2009 to 2019 on curcumin analogues, derivatives, and hybrids, as well as their therapeutic, preventic, and diagnostic applications in AD. Recent advances in the field have revealed that the phenolic hydroxyl group could contribute to the anti-amyloidogenic activity. Phenyl methoxy groups seem to contribute to the suppression of amyloid-β peptide (Aβ) and to the suppression of amyloid precursor protein (APP) andhydrophobic interactions have also revealed a growing role. Furthermore, flexible moieties, at the linker, are crucial for the inhibition of Aβ aggregation. The inhibitory activity of derivatives is increased with the expansion of the aromatic rings. The promising role of curcumin-based compounds in diagnostic imaging is highlighted. The keto-enol tautomerism seems to be a novel modification for the design of amyloid-binding agents. Molecular docking results, (Q)SAR, as well as in vitro and in vivo tests highlight the structures and chemical moieties that are correlated with specific activity. As a result, the knowledge gained from the existing research should lead to the design and synthesis ofinnovative and multitargetedcurcumin analogues, derivatives, or curcumin hybrid, which would be very useful drug and tools in medicine for both diagnosis and treatment of AD.
在全球范围内,阿尔茨海默病(AD)是最常见的影响老年人群体的神经退行性多因素疾病。如今,有几种药物(包括姜黄素)用于 AD 的治疗。姜黄素是 的主要成分,已显示出对 AD 的显著预防或治疗作用。在过去的十年中,科学界一直致力于优化其治疗特性,并改善其药代动力学特性。本综述总结了 2009 年至 2019 年关于姜黄素类似物、衍生物和混合物及其在 AD 中的治疗、预防和诊断应用的文献数据。该领域的最新进展表明,酚羟基可能有助于抗淀粉样蛋白形成活性。苯甲氧基似乎有助于抑制淀粉样蛋白-β(Aβ)和抑制淀粉样前体蛋白(APP),疏水力也显示出越来越重要的作用。此外,连接子上的柔性部分对于抑制 Aβ聚集至关重要。衍生物的抑制活性随芳环的扩展而增加。姜黄素类化合物在诊断成像中的应用前景广阔。酮-烯醇互变异构似乎是设计淀粉样蛋白结合剂的一种新修饰。分子对接结果、(QSAR)以及体外和体内测试突出了与特定活性相关的结构和化学部分。因此,从现有研究中获得的知识应导致设计和合成创新的多靶点姜黄素类似物、衍生物或姜黄素混合物,这将是医学中用于 AD 的诊断和治疗的非常有用的药物和工具。