Response of hamster circadian system to transitions between light and darkness

1986 ◽  
Vol 250 (4) ◽  
pp. R708-R711 ◽  
Author(s):  
H. E. Albers

The effects of exposure to sudden transitions from dark to light (DL) and light to dark (LD) were determined on the free-running circadian activity rhythm of Syrian hamsters. The activity rhythm was phase delayed by 1-2 h by DL transitions provided during the 12-h interval before activity onset (subjective day). In contrast, DL transitions produced phase advances of approximately 1 h 2-12 h after activity onset. LD transitions tended to produce phase advances throughout the circadian cycle. During the subjective day, LD transitions resulted in phase advances of up to 4 h. After the onset of activity, LD transitions produced phase advances of a lesser magnitude than during the subjective day. In addition, some phase delays were also observed. When the phase shifts produced by DL and LD transitions were combined additively these transitions could account for the phase shifts previously reported for brief pulses of light.

Neuroreport ◽  
1995 ◽  
Vol 6 (10) ◽  
pp. 1417-1420 ◽  
Author(s):  
Michael A. Rea ◽  
Jose Barrera ◽  
J. David Glass ◽  
Robert L. Gannon

2004 ◽  
Vol 28 (7) ◽  
pp. 1020-1027 ◽  
Author(s):  
Yuhua Z. Farnell ◽  
James R. West ◽  
Wei-Jung A. Chen ◽  
Gregg C. Allen ◽  
David J. Earnest

1980 ◽  
Vol 238 (1) ◽  
pp. R97-R101 ◽  
Author(s):  
I. Zucker ◽  
K. M. Fitzgerald ◽  
L. P. Morin

The effect of estradiol benzoate (EB) on free-running circadian activity rhythms was studied in gonadectomized hamsters maintained in constant dim illumination. EB shortened the period (tau) of the female, but not of the male circadian activity rhythm. Responsiveness of the circadian system to EB was subject to sexual differentiation. The circadian period of wheel running by female hamsters given a single injection of testosterone propionate on the day of birth did not shorten in response to EB in adulthood. This failure to respond to EB also was observed in normal male hamsters, and was different from the response shown by normal females. Preliminary data suggest that tau of the activity rhythm of males castrated on the day of birth is shortened during EB treatment in adulthood. The differential effects of estradiol on tau are related to anatomic differences between the sexes in neural connections of the substrate for circadian rhythms.


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