SAMP8 Mice as a Model of Age-Related Cognition Decline with Underlying Mechanisms in Alzheimer’s Disease
Abstract
Alzheimer's disease (AD) is a highly age-related cognitive decline frequently attacking the elderly. Senescence-accelerated mouse-prone 8 (SAMP8) is an ideal model to study AD, displaying age-related learning and memory disorders. SAMP8 mice exhibit most features of pathogenesis of AD, including an abnormal expression of anti-aging factors, oxidative stress, inflammation, amyloid-β (Aβ) deposits, tau hyperphosphorylation, endoplasmic reticulum stress, abnormal autophagy activity, and disruption of intestinal flora. SAMP8 mice, therefore, have visualized the understanding of AD, and also provided effective ways to find new therapeutic targets. This review focused on the age-related pathogenesis in SAMP8 mice, to advance the understanding of age-related learning and memory decline and clarify the mechanisms. Furthermore, this review will provide extensive foundations for SAMP8 mice used in therapeutics for AD.
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The SAMP8 mice exhibit reduced expression and lower activity of anti-aging factors including sirtuin/Sirt, FoxOs, and Klothos.
“The SAMP8 mice exhibit reduced expression and lower activity of anti-aging factors including silent information regulator type (sirtuin/Sirt), Forkhead box class O (FoxOs), and Klothos.”
From Inflammation and aging: signaling pathways and intervention therapies (2023) · cites this paper as [301]
The SAMP8 mouse strain is considered an excellent model for investigating Alzheimer's disease (AD).
“On the other hand, the SAMP8 mouse strain is considered an excellent model for investigating Alzheimer’s disease (AD), a cognitive decline disorder that predominantly affects the elderly.”
From Inflammation and aging: signaling pathways and intervention therapies (2023) · cites this paper as [301]
These factors play crucial roles in the aging process.
“These factors play crucial roles in the aging process.301”
From Inflammation and aging: signaling pathways and intervention therapies (2023) · cites this paper as [301]
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- Authors
- Liu, B., Liu, J., & Shi, J.-S.
- Affiliations
- Zunyi Medical University (CN)
- Key Laboratory of Basic Pharmacology of Ministry of Education and Joint International Research Lab of Ethnomedicine of Ministry of Education, Zunyi Medical University, Zunyi, China
- ORCID
- Liu, Jie
- Venue
- Journal of Alzheimer's Disease
- Publisher
- SAGE Publications
- Published
- 2020-05-19
- Volume
- 75
- Issue
- 2
- Pages
- 385-395
- ISSN
- 1387-2877 (ISSN-L)
- 1875-8908
- OpenAlex
- W3016854391
- Cited by
- 156
- References
- 115
- Citations by year
- 2026: 12 · 2025: 34 · 2024: 43 · 2023: 24 · 2022: 23 · 2021: 16 · 2020: 4
- FWCI
- 2.20
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Alzheimer s Disease (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Antioxidants, Aging, Portulaca oleracea
- Keywords
- SAMP8 mice, Alzheimer's disease
- MeSH terms
- Aging, Alzheimer Disease, Animals, Brain, Disease Models, Animal, Amyloid beta-Peptides, Neurofibrillary Tangles, tau Proteins, Mice, Cognitive Dysfunction
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