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Age-related difference in nociceptive behavior between SAMP6 and SAMR1 strains
Kimie Niimi1, Eiki Takahashi, Chitoshi Itakura
1Brain Science and Life Technology Research Foundation, 1-28-12 Narimasu, Itabashi, Tokyo 175-0094, Japan.
Neuroscience Letters
|August 16, 2008
Summary
Senescence accelerated prone mouse 6 (SAMP6) mice show normal pain responses at younger ages. However, older SAMP6 mice exhibit altered pain signaling, suggesting tissue-specific aging effects and potential for studying age-related pain mechanisms.
Area of Science:
- Gerontology
- Neuroscience
- Pain Research
Background:
- Senescence accelerated prone mouse 6 (SAMP6) mice model accelerated aging.
- SAMP6 mice display reduced bone mass and memory deficits at later ages.
- Nervous system function changes may occur early in SAMP6 mice.
Purpose of the Study:
- To investigate age-related abnormalities in nociceptive (pain) transmission in SAMP6 mice.
- To compare pain responses in SAMP6 mice with senescence accelerated resistant mouse 1 (SAMR1) controls.
- To determine if SAMP6 mice exhibit altered responses to mechanical, thermal, and chemical stimuli.
Main Methods:
- Utilized von Frey, hot plate, and formalin paw tests to assess nociception.
- Compared SAMP6 and SAMR1 mice at 1 and 4 months of age.
- Analyzed responses to mechanical, thermal, and chemical pain stimuli.
Main Results:
- SAMP6 and SAMR1 mice showed similar responses in von Frey and hot plate tests.
- In the formalin paw test, 1-month-old mice had comparable responses.
- 4-month-old SAMP6 mice displayed attenuated phase 2 (chemically induced) pain response but normal phase 1 response.
Conclusions:
- The onset of age-related phenotypes in SAMP6 mice varies across different tissues.
- SAMP6 mice demonstrate altered nociceptive transmission with age.
- SAMP6 mice are a valuable model for investigating age-related pain mechanisms.

