Transcriptome analysis of the aged SAMP8 mouse model of Alzheimer’s disease reveals novel molecular targets of formononetin protection

Neuroinflammation and decreased antioxidant and SIRT-1 signaling contributed to cognitive deficits in aged SAMP8 mice, which are potential therapeutic targets of formononetin in combination with other therapies.

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Publication Details

Journal
Frontiers in Pharmacology
Published
2024-08-21
DOI
https://doi.org/10.3389/fphar.2024.1440515
Citations
6
Primary Topic
Alzheimer's disease research and treatments
Type
article
Field-Weighted Citation Impact
1.96

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article

Transcriptome analysis of the aged SAMP8 mouse model of Alzheimer’s disease reveals novel molecular targets of formononetin protection

Jie Liu, Bo Liu, Di Cui, Jing-Shan Shi
6 citations
Frontiers in Pharmacology
Alzheimer's disease research and treatments
1.96
article

Transcriptome analysis of the aged SAMP8 mouse model of Alzheimer’s disease reveals novel molecular targets of formononetin protection

Jie Liu, Bo Liu, Di Cui, Jing-Shan Shi
article en
6 citations

Abstract

Neuroinflammation and decreased antioxidant and SIRT-1 signaling contributed to cognitive deficits in aged SAMP8 mice, which are potential therapeutic targets of formononetin in combination with other therapies.

Frontiers in PharmacologyVol. 15
Zunyi Medical University (CN)
Guizhou Science and Technology Department
Good health and well-being
Openalex Percentile: Top 13%
Alzheimer's disease research and treatments
1.96
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