Neuropathological studies on strains of senescence-accelerated mice (SAM) with age-related deficits in learning and memory
Abstract
In a series of inbred Senescence-Accelerated mice (SAM) strains, accelerated-senescence prone SAMP substrains show early onset and rapid advancement of senescence. SAMP8 and SAMP10, in particular, exhibit a significant age-related deterioration in memory and learning for passive and active avoidance tasks with, respectively, a low and high incidence of systemic senile amyloidosis. In the brains of both SAMP8 and SAMP10 strains, we have found numerous morphological alterations. Here we review the changes seen in both neuronal or glial components in SAMP8/P10 brains. They may serve as markers of the neuronal degeneration leading to the deficits in learning and memory.
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SAMP8 mice have a shortened life-span, learning and memory deficits, features of AMD, and no signs of brain atrophy.
“The SAMP8 mice have a shortened life-span, learning and memory deficits, features of AMD, and no signs of brain atrophy”
From Retinal ultrastructure of murine models of dry age-related macular degeneration (AMD) (2010) · cites this paper as Kawamata et al., 1997
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- Authors
- Kawamata, T.
- Affiliations
- Kyoto University (JP)
- Corresponding author
- Kawamata, T
- Venue
- Experimental Gerontology
- Publisher
- Elsevier BV
- Published
- 1997-04
- Volume
- 32
- Issue
- 1-2
- Pages
- 161-169
- ISSN
- 0531-5565 (ISSN-L)
- OpenAlex
- W2115072309
- Cited by
- 72
- References
- 47
- Citations by year
- 2025: 1 · 2023: 2 · 2021: 3 · 2018: 2 · 2017: 1 · 2016: 3 · 2015: 2 · 2014: 2 · 2013: 7 · 2012: 2
- FWCI
- 0.78
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Experimental Gerontology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Antioxidants, Aging, Portulaca oleracea
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Keywords
- senescence-accelerated mice, SAMP8 mice, age-related memory impairment, learning deficits, senile amyloidosis, neurodegeneration, glial changes, brain structure, aging, avoidance learning
- MeSH terms
- Aging, Animals, Learning Disabilities, Memory Disorders, Mice, Inbred Strains, Neurons, Phenotype, Time Factors, Neuroaxonal Dystrophies, Mice
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