| Literature DB >> 26844592 |
Hyek Jin Kwon1,2, Moon-Yong Cha3, Dokyoon Kim1, Dong Kyu Kim3, Min Soh1,2, Kwangsoo Shin1,2, Taeghwan Hyeon1,2, Inhee Mook-Jung3.
Abstract
Mitochondrial oxidative stress is a key pathologic factor in neurodegenerative diseases, including Alzheimer's disease. Abnormal generation of reactive oxygen species (ROS), resulting from mitochondrial dysfunction, can lead to neuronal cell death. Ceria (CeO2) nanoparticles are known to function as strong and recyclable ROS scavengers by shuttling between Ce(3+) and Ce(4+) oxidation states. Consequently, targeting ceria nanoparticles selectively to mitochondria might be a promising therapeutic approach for neurodegenerative diseases. Here, we report the design and synthesis of triphenylphosphonium-conjugated ceria nanoparticles that localize to mitochondria and suppress neuronal death in a 5XFAD transgenic Alzheimer's disease mouse model. The triphenylphosphonium-conjugated ceria nanoparticles mitigate reactive gliosis and morphological mitochondria damage observed in these mice. Altogether, our data indicate that the triphenylphosphonium-conjugated ceria nanoparticles are a potential therapeutic candidate for mitochondrial oxidative stress in Alzheimer's disease.Entities:
Keywords: Alzheimer’s disease; ceria nanoparticles; mitochondria; reactive oxygen species; therapeutic agents
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Year: 2016 PMID: 26844592 DOI: 10.1021/acsnano.5b08045
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881