Comprehensive behavioural study of senescence-accelerated mouse prone 8 and senescence-accelerated mouse prone 10

Aging is the strongest risk factor for neurodegenerative diseases and has been implicated in important changes in the brain. Rodents, such as mice, have been used to understand age-related changes in brain function, and aging has been studied using senescence-accelerated mouse (SAM) strains. Accumulating evidence indicates that SAM-prone (SAMP)8 and SAMP10 strains have learning disabilities. However, in previous studies, these strains were not subjected to a series of behavioural tests. In behavioural experiments, it is necessary to conduct a behavioural test battery to consider various aspects, including sources of variability and experimental interference. This study aimed to comprehensively characterize behavioural abnormalities in SAMP8 and SAMP10 mice using a standardized battery of behavioural tests. We conducted a series of behavioural tests (neuromuscular strength, elevated plus maze, light-dark transition, open field, Y-maze, and passive avoidance tests) to investigate behaviour in SAMP8 and SAMP10 strains. We used 12-month-old male mice in this study. SAMP8 and SAMP10 mice exhibited abnormal behaviour in the present behavioural tests. Body weight, body temperature, muscle strength, and motor learning differed between SAMP8 or SAMP10 and SAMR1 mice. These differences may underlie variations in anxiety-like behaviours and locomotor activity. Together, these findings highlight the utility of SAMP8 and SAMP10 mice as models for studying age-related functional decline in the brain.

Authors

Institutions

Publication Details

Journal
Translational Medicine of Aging
Published
2025-01-01
DOI
https://doi.org/10.1016/j.tma.2025.08.003
Primary Topic
Neuroscience and Neuropharmacology Research
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Comprehensive behavioural study of senescence-accelerated mouse prone 8 and senescence-accelerated mouse prone 10

Shinji Murakami, Yosuke Matsumoto, Hiroshi Ueno, Tetsuji Miyazaki et al.
Translational Medicine of Aging
Neuroscience and Neuropharmacology Research
article

Comprehensive behavioural study of senescence-accelerated mouse prone 8 and senescence-accelerated mouse prone 10

Shinji Murakami, Yosuke Matsumoto, Hiroshi Ueno, Tetsuji Miyazaki, Yu Takahashi, Kenta Wani, Takeshi Ishihara, Motoi Okamoto
article en

Abstract

Aging is the strongest risk factor for neurodegenerative diseases and has been implicated in important changes in the brain. Rodents, such as mice, have been used to understand age-related changes in brain function, and aging has been studied using senescence-accelerated mouse (SAM) strains. Accumulating evidence indicates that SAM-prone (SAMP)8 and SAMP10 strains have learning disabilities. However, in previous studies, these strains were not subjected to a series of behavioural tests. In behavioural experiments, it is necessary to conduct a behavioural test battery to consider various aspects, including sources of variability and experimental interference. This study aimed to comprehensively characterize behavioural abnormalities in SAMP8 and SAMP10 mice using a standardized battery of behavioural tests. We conducted a series of behavioural tests (neuromuscular strength, elevated plus maze, light-dark transition, open field, Y-maze, and passive avoidance tests) to investigate behaviour in SAMP8 and SAMP10 strains. We used 12-month-old male mice in this study. SAMP8 and SAMP10 mice exhibited abnormal behaviour in the present behavioural tests. Body weight, body temperature, muscle strength, and motor learning differed between SAMP8 or SAMP10 and SAMR1 mice. These differences may underlie variations in anxiety-like behaviours and locomotor activity. Together, these findings highlight the utility of SAMP8 and SAMP10 mice as models for studying age-related functional decline in the brain.

Translational Medicine of AgingVol. 9
Okayama University (JP), Kawasaki Medical School (JP), Kawasaki University of Medical Welfare (JP)
Japan Society for the Promotion of Science
Openalex Percentile: Top 78%
Neuroscience and Neuropharmacology Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.