Journal of Alzheimer's Disease
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Home > An Optimized Combination of Ginger and Peony Root Effectively Inhibits Amyloid-β Accumulation and Amyloid-β-Mediated Pathology in AβPP/PS1 Double-Transgenic Mice.

TitleAn Optimized Combination of Ginger and Peony Root Effectively Inhibits Amyloid-β Accumulation and Amyloid-β-Mediated Pathology in AβPP/PS1 Double-Transgenic Mice.
Publication TypeJournal Article
Year of Publication2016
AuthorsLim, S, Choi, JGyu, Moon, M, Kim, HGeun, Lee, W, Bak, H-R, Sung, H, Park, CHye, Kim, SYeou, Oh, MSook
JournalJ Alzheimers Dis
Volume50
Issue1
Pagination189-200
Date Published2016
ISSN1875-8908
KeywordsAlzheimer Disease, Amyloid beta-Peptides, Amyloid beta-Protein Precursor, Analysis of Variance, Animals, Cyclooxygenase 2, Disease Models, Animal, Dose-Response Relationship, Drug, Ginger, Glial Fibrillary Acidic Protein, Humans, Male, Mice, Mice, Transgenic, Mutation, Paeonia, Phytotherapy, Plant Preparations, Plaque, Amyloid, Presenilin-1
Abstract

The progressive aggregation of amyloid-β protein (Aβ) into senile plaques is a major pathological factor of Alzheimer's disease (AD) and is believed to result in memory impairment. We aimed to investigate the effect of an optimized combination of ginger and peony root (OCGP), a standardized herbal mixture of ginger and peony root, on Aβ accumulation and memory impairment in amyloid-β protein precursor (AβPP)/presenilin 1 (PS1) double-transgenic mice. In an in vitro thioflavin T fluorescence assay, 100 μg/ml OCGP inhibited Aβ accumulation to the same extent as did 10 μM curcumin. Furthermore, AβPP/PS1 double-transgenic mice treated with OCGP (50 or 100 mg/kg/day given orally for 14 weeks) exhibited reduced Aβ plaque accumulation in the hippocampus and lower levels of glial fibrillary acid protein and cyclooxygease-2 expression compared with vehicle-treated controls. These results suggest that OCGP may prevent memory impairment in AD by inhibiting Aβ accumulation and inflammation in the brain.

DOI10.3233/JAD-150839
Alternate JournalJ. Alzheimers Dis.
PubMed ID26639976
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