Enhanced neuroprotection of anthocyanin-loaded PEG-gold nanoparticles against A beta(1-42)-induced neuroinflammation and neurodegeneration via the NF-B-K /JNK/GSK3 beta signaling pathway

초록

Amyloid-beta (A beta(1-42)) plaques and neurofibrillary tangles (NFTs) are the main hallmarks considered to be associated with neuroinflammation in Alzheimer's disease (AD). Recently, nanoparticle-based targeted drug delivery approaches have been found to be a useful tool in the neurotherapeutics field. Therefore, we examined and compared the neuroprotective effect of anthocyanins alone and anthocyanin-loaded poly (ethylene glycol)-gold nanoparticles (PEG-AuNPs) in A beta(1-42)-injected mouse and in vitro models of AD. We determined that anthocyanins alone or conjugated with PEG-AuNPs (AnPEG-AuNPs) reduced A beta(1-42)-induced neuroinflammatory and neuroapoptotic markers via inhibiting the p-JNK/NF-kappa B/p-GSK3 beta pathway in both in vivo and in vitro AD models. However, anthocyanins loaded with PEG-AuNPs were more effective compared to anthocyanins alone. Taken together, these results demonstrate that PEG-coated gold anthocyanins nanoparticles could be a new therapeutic agent in the field of nanomedicine to prevent neurodegenerative diseases such as AD. (C) 2017 Elsevier Inc. All rights reserved.

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