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Imaging hydrogen peroxide in Alzheimer’s disease via cascade signal amplification

In brains of Alzheimer’s disease (AD), reactive oxygen species (ROS) levels are significantly higher than that of healthy brains. Evidence suggests that, during AD onset and progression, a vicious cycle revolves around amyloid beta (Aβ) production, aggregation, plaque formation, microglia/immunologi...

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Detalles Bibliográficos
Autores principales: Yang, Jian, Yang, Jing, Liang, Steven H., Xu, Yungen, Moore, Anna, Ran, Chongzhao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5071891/
https://www.ncbi.nlm.nih.gov/pubmed/27762326
http://dx.doi.org/10.1038/srep35613
Descripción
Sumario:In brains of Alzheimer’s disease (AD), reactive oxygen species (ROS) levels are significantly higher than that of healthy brains. Evidence suggests that, during AD onset and progression, a vicious cycle revolves around amyloid beta (Aβ) production, aggregation, plaque formation, microglia/immunological responses, inflammation, and ROS production. In this cycle, ROS species play a central role, and H(2)O(2) is one of the most important ROS species. In this report, we have designed a fluorescent imaging probe CRANAD-88, which is capable of cascade amplifying near infrared fluorescence (NIRF) signals at three levels upon interacting with H(2)O(2) in AD brains. We demonstrated that the amplification was feasible in vitro and in vivo. Remarkably, we showed that, for the first time, it was feasible to monitor the changes of H(2)O(2) concentrations in AD brains before and after treatment with an H(2)O(2) scavenger. Our method opens new revenues to investigate H(2)O(2) in AD brains and can be very instructive for drug development.