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用于通过单光子发射计算机断层扫描(SPECT)对淀粉样β斑块进行成像的乙氧基化和烯丙氧基化查耳酮衍生物的合成与评价

Synthesis and evaluation of ethyleneoxylated and allyloxylated chalcone derivatives for imaging of amyloid β plaques by SPECT.

作者信息

Fuchigami Takeshi, Yamashita Yuki, Haratake Mamoru, Ono Masahiro, Yoshida Sakura, Nakayama Morio

机构信息

Department of Hygienic Chemistry, Graduate School of Biomedical Sciences, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852-8521, Japan.

Department of Hygienic Chemistry, Graduate School of Biomedical Sciences, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852-8521, Japan.

出版信息

Bioorg Med Chem. 2014 May 1;22(9):2622-8. doi: 10.1016/j.bmc.2014.03.032. Epub 2014 Mar 27.

DOI:10.1016/j.bmc.2014.03.032
PMID:24717291
Abstract

We report radioiodinated chalcone derivatives as new SPECT imaging probes for amyloid β (Aβ) plaques. The monoethyleneoxy derivative 2 and allyloxy derivative 8 showed a high affinity for Aβ(1-42) aggregates with Ki values of 24 and 4.5 nM, respectively. Fluorescent imaging demonstrated that 2 and 8 clearly stained thioflavin-S positive Aβ plaques in the brain sections of Tg2576 transgenic mice. In vitro autoradiography revealed that [(125)I]2 displayed no clear accumulation toward Aβ plaques in the brain sections of Tg2576 mice, whereas the accumulation pattern of [(125)I]8 matched with the presence of Aβ plaques both in the brain sections of Tg2576 mice and an AD patient. In biodistribution studies using normal mice, [(125)I]2 showed preferable in vivo pharmacokinetics (4.82%ID/g at 2 min and 0.45%ID/g at 60 min), while [(125)I]8 showed only a modest brain uptake (1.62%ID/g at 2 min) with slow clearance (0.56%ID/g at 60 min). [(125)I]8 showed prospective binding properties for Aβ plaques, although further structural modifications are needed to improve the blood brain barrier permeability and washout from brain.

摘要

我们报道了放射性碘化查尔酮衍生物作为用于淀粉样β(Aβ)斑块的新型单光子发射计算机断层显像(SPECT)成像探针。单乙氧基衍生物2和烯丙氧基衍生物8对Aβ(1-42)聚集体表现出高亲和力,其抑制常数(Ki)值分别为24和4.5 nM。荧光成像表明,2和8能清晰地对Tg2576转基因小鼠脑切片中的硫黄素-S阳性Aβ斑块进行染色。体外放射自显影显示,[(125)I]2在Tg2576小鼠脑切片中未显示出对Aβ斑块的明显聚集,而[(125)I]8的聚集模式与Tg2576小鼠脑切片和一名阿尔茨海默病(AD)患者脑切片中Aβ斑块的存在情况相匹配。在使用正常小鼠的生物分布研究中,[(125)I]2显示出较好的体内药代动力学(2分钟时为4.82%注射剂量/克,60分钟时为0.45%注射剂量/克),而[(125)I]8仅表现出适度的脑摄取(2分钟时为1.62%注射剂量/克)且清除缓慢(60分钟时为0.56%注射剂量/克)。[(125)I]8显示出对Aβ斑块的潜在结合特性,尽管需要进一步的结构修饰以改善血脑屏障通透性和从脑中的清除率。

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