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  5. Anti-Inflammatory and Tau Phosphorylation-Inhibitory Effects of Eupatin
 
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Anti-Inflammatory and Tau Phosphorylation-Inhibitory Effects of Eupatin

Journal
Molecules (Basel, Switzerland)
Journal Volume
25
Journal Issue
23
Date Issued
2020
Author(s)
Chou C.-H.
Hsu K.-C.
Lin T.E.
CHIA-RON YANG  
DOI
10.3390/molecules25235652
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85097120675&doi=10.3390%2fmolecules25235652&partnerID=40&md5=8dcd299146321a98a7b887c65679bcd0
https://scholars.lib.ntu.edu.tw/handle/123456789/565263
Abstract
Alzheimer's disease (AD), which is among the most prevalent neurodegenerative diseases, manifests as increasing memory loss and cognitive decline. Tau phosphorylation and aggregation are strongly linked to neurodegeneration, as well as associated with chronic neuroinflammatory processes. The anti-inflammation effects of natural products have led to wide recognition of their potential for use in treating and preventing AD. This study investigated whether eupatin, a polymethoxyflavonoid found in Artemisia species, has inhibitory effects on neuroinflammation and tau phosphorylation. We treated mouse macrophages and microglia cells with lipopolysaccharides (LPSs) to activate inflammatory signals, and we treated neuronal cells with a protein phosphatase 2A inhibitor, okadaic acid (OA), or transfection with pRK5-EGFP-Tau P301L plasmid to induce tau phosphorylation. The results indicated that eupatin significantly reduced the LPS-induced protein expression and phosphorylation of p65 and inducible nitric oxide synthase as well as downstream products interleukin 6 and nitrite, respectively. Furthermore, eupatin markedly inhibited the expression of phospho-tau in response to OA treatment and plasmid transfection. We discovered that this inhibition was achieved through the inhibition of glycogen synthase kinase 3β (GSK3β), and molecular docking results suggested that eupatin can sufficiently bind to the GSK3β active site. Our results demonstrate that eupatin has neuroprotective effects, making it suitable for AD treatment.
SDGs

[SDGs]SDG3

Type
journal article

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