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ID 69232
著者
Hu, Xinran Department of Neurology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Morihara, Ryuta Department of Neurology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University ORCID Kaken ID researchmap
Fukui, Yusuke Department of Neurology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Bian, Yuting Department of Neurology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Sun, Hongming Department of Neurology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Ota-Elliott, Ricardo Satoshi Department of Neurology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Ishiura, Hiroyuki Department of Neurology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Abe, Koji National Center Hospital, National Center of Neurology and Psychiatry
Yamashita, Toru Department of Neurology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University ORCID Kaken ID researchmap
抄録
In recent years, many researchers have focused on natural compounds that can effectively delay symptoms of Alzheimer’s disease (AD). The spearmint extract Neumentix, which is rich in phenolic compounds, has been shown to reduce inflammatory responses and oxidative stress in mice. However, the effect of Neumentix on AD has not been thoroughly studied. In this study, APP23 transgenic female and male mice were administered Neumentix orally from 4 to 18 months of age at a dosage of 2.65 g/kg/day (containing 0.41 g/kg/day of rosmarinic acid). The impact was evaluated by behavioral tests and histological analyses and compared with APP23 mice to which Neumentix was not administered. The results showed that Neumentix administration increased the survival rate of APP23 mice and effectively reduced Aβ accumulation by enhancing its phagocytosis by microglial cells. These findings suggest that Neumentix is a potential natural nutritional treatment for improving the progression of AD.
キーワード
Alzheimer's disease
Amyloid-beta
Inflammation
Neumentix
Phagocytosis
Survival rate
備考
© 2025 Elsevier B.V. This manuscript version is made available under the CC-BY-NC-ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0
This fulltext file will be available in Jun. 2026.
発行日
2025-09
出版物タイトル
Brain Research
1863巻
出版者
Elsevier BV
開始ページ
149752
ISSN
0006-8993
資料タイプ
学術雑誌論文
言語
英語
OAI-PMH Set
岡山大学
著作権者
© 2025 Elsevier B.V.
論文のバージョン
author
PubMed ID
DOI
Web of Science KeyUT
関連URL
isVersionOf https://doi.org/10.1016/j.brainres.2025.149752
ライセンス
https://creativecommons.org/licenses/by-nc-nd/4.0
助成情報
21K19572: 脳内炎症を可視化する挑戦的融合的 in vivo 分子イメージング法の確立 ( 独立行政法人日本学術振興会 / Japan Society for the Promotion of Science )
22K17799: ダイレクトリプログラミングによる脳梗塞モデルマウスの海馬神経細胞と認知機能の再生 ( 独立行政法人日本学術振興会 / Japan Society for the Promotion of Science )
21K15190: FUS相転移を制御するアルギニンメチル化の解明 ( 独立行政法人日本学術振興会 / Japan Society for the Promotion of Science )
( 国立研究開発法人日本医療研究開発機構 / Japan Agency for Medical Research and Development )