| Literature DB >> 26073008 |
Takeshi Fuchigami1, Ayaka Ogawa2, Yuki Yamashita2, Mamoru Haratake3, Hiroyuki Watanabe4, Masahiro Ono4, Masao Kawasaki2, Sakura Yoshida2, Morio Nakayama5.
Abstract
We report here the development of radioiodinated styrylchromone derivatives with alkoxy groups as single photon emission computed tomography (SPECT) imaging probes for cerebral amyloid-β (Aβ) plaques. Among the derivatives, the methoxy derivative 14 and the dimethoxy derivative 15 displayed relatively high affinity for the Aβ(1-42) aggregates with K(i) values of 22 and 46 nM, respectively. Fluorescent imaging demonstrated that 14 and 15 clearly labeled thioflavin-S positive Aβ plaques in the brain sections of Tg2576 transgenic mice. In the in vivo studies, [(125)I]14 and [(125)I]15 showed high initial brain uptake expressed as the percentage of the injected dose per gram (2.25% and 2.49% ID/g at 2 min, respectively) with favorable clearance (0.12% and 0.20% ID/g at 180 min, respectively) from the brain tissue of normal mice. Furthermore, in vitro autoradiography confirmed that [(125)I]15 binds thioflavin-S positive regions in Tg2576 mouse brain sections. The derivative 15 may be a potential scaffold for the development of in vivo imaging probes targeting Aβ plaques in the brain. In particular, further structural modifications are required to improve the compounds binding affinity for Aβ.Entities:
Keywords: Alzheimer’s disease; Amyloid-β plaque; Single photon emission computed tomography (SPECT); Styrylchromone
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Year: 2015 PMID: 26073008 DOI: 10.1016/j.bmcl.2015.05.048
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823