Curcumin Complex Analogues as Near-Infrared Fluorescent Probes for Monitoring all Aβ Species in the Early Alzheimer's Disease Model

被引:20
作者
Ge, Yiran [1 ]
Zeng, Fantian [1 ]
Sun, Gaofeng [2 ]
Peng, Kewen [1 ]
Li, Xiao [2 ]
Yu, Huijuan [3 ]
Cheng, Chao [2 ]
Xu, Yungen [1 ]
Yang, Jian [4 ]
机构
[1] China Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Peoples R China
[2] Shanghai Changhai Hosp, Dept Nucl Med, Shanghai 200433, Peoples R China
[3] Guangdong Univ Technol, Sch Chem Engn & Light Ind, Guangzhou 510006, Peoples R China
[4] Shanghai Univ, Shanghai Engn Res Ctr Organ Repair, Sch Med, Shanghai 200444, Peoples R China
基金
中国国家自然科学基金;
关键词
amyloid beta-peptide; Alzheimer's disease; curcumin complex analogues; near-infrared fluorescent probe; SOLUBLE-PROTEIN OLIGOMERS; IN-VIVO DETECTION; AMYLOID-BETA; TOXICITY; HYPOTHESIS; COPPER; COMMON; MRI;
D O I
10.1021/acschemneuro.1c00419
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aggregation of amyloid beta-peptide (A beta) is closely related to the pathology of Alzheimer's disease (AD). In this pathology, the beginning stage is characterized by excessive accumulation of A beta monomers due to imbalanced A beta in the process of clearance. The A beta peptide exists in many forms such as soluble and insoluble A beta species, both of which coexist during the progression of AD and contribute to AD pathology. Thus, probes capable of monitoring all A beta species are highly desirable. While there are several fluorescent probes for detecting insoluble A beta, it is still challenging to monitor all A beta forms by using probes. Here, we describe a near-infrared fluorescent chemical probe, termed AD-1, developed through complexation of curcumin analogues with a stabilizer, which has good photophysical properties and shows high binding to all A beta species in solution tests. Furthermore, AD-1 exhibited good blood-brain barrier penetrating ability and low cytotoxicity. More importantly, it was successfully applied to 4-month-young APP/PS1 mice imaging noninvasively.
引用
收藏
页码:3683 / 3689
页数:7
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