Effects of aging on the circadian rhythm of wheel-running activity in C57BL/6 mice
V. S. Valentinuzzi, K. Scarbrough, J. S. Takahashi and F. W. Turek Department of Neurobiology and Physiology, Northwestern University, Evanston, Illinois 60208, USA. The effects of age on the circadian clock system have been extensively studied, mainly in two rodent species, the laboratory rat and t...
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Veröffentlicht in: | American journal of physiology. Regulatory, integrative and comparative physiology integrative and comparative physiology, 1997-12, Vol.273 (6), p.1957-R1964 |
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Zusammenfassung: | V. S. Valentinuzzi, K. Scarbrough, J. S. Takahashi and F. W. Turek
Department of Neurobiology and Physiology, Northwestern University, Evanston, Illinois 60208, USA.
The effects of age on the circadian clock system have been extensively
studied, mainly in two rodent species, the laboratory rat and the golden
hamster. However, less information is available on how aging alters
circadian rhythmicity in a commonly studied rodent animal model, the mouse.
Therefore, in the present study we compared the rhythm of wheel-running
activity in adult (6-9 mo) and old (19-22 mo) C57BL/6J mice maintained
under different lighting conditions for a period of 4 mo. During this
period, mice were subjected to phase advances and phase delays of the
light-dark (LD) cycle and eventually to constant darkness (DD). In LD (12 h
light, 12 h dark), old mice exhibited delayed activity onset relative to
light offset and an increase in the variability of activity onset compared
with adult mice. After a 4-h phase advance of the LD cycle, old mice took
significantly longer to reentrain their activity rhythm when compared with
adult animals. Old mice also demonstrated a decline in the number of wheel
revolutions per day and a tendency toward a decrease in the length of the
active phase. An increase in fragmentation of activity across the 24-h day
was obvious in aging animals, with bouts of activity being shorter and
longer rest periods intervening between them. No age difference was
detected in the maximum intensity of wheel-running activity. In DD, the
free-running period was significantly longer in old mice compared with
adults. In view of the rapidly expanding importance of the laboratory mouse
for molecular and genetic studies of the mammalian nervous system, the
present results provide a basis at the phenotypic level to begin to apply
genetic methods to the analysis of circadian rhythms and aging in mammals. |
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ISSN: | 0363-6119 0002-9513 1522-1490 |
DOI: | 10.1152/ajpregu.1997.273.6.r1957 |