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Abstract
Circadian clock gene expression is significantly modified in the SCN and peripheral tissues of aged mice.
- Aged mice show preserved circadian profiles of core clock gene expression in the SCN but impaired expression in peripheral tissues.
- Both primary and secondary clock loop components are affected by aging, indicating complex changes in circadian rhythm regulation.
- Specific changes in secondary clock loop components, such as Rev-erbα, are observed in the SCN of older mice.
- The primary clock loop experiences alterations in the liver, while the heart exhibits only minor changes in clock gene expression.
- Findings suggest that aging impacts circadian output through distinct modifications in different tissue types.
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