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论文类型：期刊论文

发表时间：2015-01-01

发表刊物：RSC ADVANCES

收录刊物：SCIE、EI、Scopus

卷号：5

期号：38

页面范围：30197-30205

ISSN号：2046-2069

摘要：Amyloid-beta (A beta) fibrillation is a crucial factor in the etiology of Alzheimer's disease (AD). Curcumin has been widely studied and considered as a promising drug for AD treatment, but its molecular mechanism in inhibiting A beta aggregation is still not clearly defined. In the present study, quartz crystal microbalance with dissipation monitoring (QCM-D) was used to analyse the growth behaviors of A beta fibrils in the presence and absence of curcumin. The viscoelasticity properties that reflect the structural information of the resulting A beta aggregates were also analysed using a Delta D/Delta F plot. It was found that the presence of curcumin could accelerate the deposition process of A beta monomers on the initially immobilized fibrils, with the growth rate being 21.1-120.6% higher than that of the control. Viscoelasticity analysis showed that curcumin-induced A beta aggregates exhibited a much more flexible structure than that of the initial fibrils, and the degree of this kind of structural conversion was related to the concentration of curcumin. Importantly, we found that further deposition of A beta monomers on these loosely constructed A beta aggregates was significantly inhibited, with the growth rate being only 34.2% of initial rate. Therefore, the QCM-D study demonstrated that curcumin inhibited the growth of A beta fibrils through a process that led to the structural conversion of the growing fibrils, and directed these fibrils to an off-pathway aggregation, which may hinder the formation of long A beta fibrils that could cause neuronal damage.