Curcumin in Health and Diseases: Alzheimer's Disease and Curcumin Analogues, Derivatives, and Hybrids

被引:128
作者
Chainoglou, Eirini [1 ]
Hadjipavlou-Litina, Dimitra [1 ]
机构
[1] Aristotle Univ Thessaloniki, Dept Pharmaceut Chem, Sch Pharm, Fac Hlth Sci, Thessaloniki 54124, Greece
关键词
Alzheimer'sdisease; curcumin analogues; derivatives; hybrids; diagnosis; therapy; MULTITARGET-DIRECTED LIGANDS; AMYLOID-BETA AGGREGATION; OXIDATIVE STRESS; BIOLOGICAL EVALUATION; ACETYLCHOLINESTERASE ACTIVITY; CROSS-LINKING; INHIBITION; DESIGN; ACID; POTENT;
D O I
10.3390/ijms21061975
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
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 Curcuma longa, 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-beta peptide (A beta(42)) 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 A beta 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 hybrids, which would be very useful drug and tools in medicine for both diagnosis and treatment of AD.
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页数:55
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