Formal properties of the circadian system underlying photoperiodic time-measurement in Japanese quail

1982 ◽  
Vol 145 (3) ◽  
pp. 381-390 ◽  
Author(s):  
S. M. Simpson ◽  
B. K. Follett
1997 ◽  
Vol 272 (1) ◽  
pp. R172-R182 ◽  
Author(s):  
H. Underwood ◽  
T. Siopes ◽  
K. Edmonds

Experiments were conducted to determine the anatomic and physiological basis of the dual-oscillator circadian system of female Japanese quail. After blocking of ocular light perception by eye-patching, the circadian body temperature rhythm dissociates into two circadian components in continuous lighting (LL). One component free runs with a period significantly shorter than 24 h [mean period (tau) = 22.7 h] and is driven by an ocular pacemaker, whereas the other component free runs with a period significantly longer than 24 h (tau = 26.3 h). The long free-running rhythm is driven by the same circadian clock that drives the circadian rhythm of ovulation. The expression of the long free-running rhythm in LL depends on the presence of the ovary: body temperature rhythmicity is abolished by ovariectomy. The two free-running oscillators in eye-patched birds showed evidence of mutual interaction. Significantly, the phase relationships that occur as the two oscillators interact can determine whether or not ovulation occurs. The results are discussed in terms of an "internal coincidence" mechanism for photoperiodic time measurement.


1995 ◽  
pp. 95-105 ◽  
Author(s):  
Michael H. Hastings ◽  
Elizabeth S. Maywood ◽  
Francis J. P. Ebling

2008 ◽  
pp. S139-S148
Author(s):  
A Sumová ◽  
Z Bendová ◽  
M Sládek ◽  
R El-Hennamy ◽  
K Matějů ◽  
...  

The circadian system controls the timing of behavioral and physiological functions in most organisms studied. The review addresses the question of when and how the molecular clockwork underlying circadian oscillations within the central circadian clock in the suprachiasmatic nuclei of the hypothalamus (SCN) and the peripheral circadian clocks develops during ontogenesis. The current model of the molecular clockwork is summarized. The central SCN clock is viewed as a complex structure composed of a web of mutually synchronized individual oscillators. The importance of development of both the intracellular molecular clockwork as well as intercellular coupling for development of the formal properties of the circadian SCN clock is also highlighted. Recently, data has accumulated to demonstrate that synchronized molecular oscillations in the central and peripheral clocks develop gradually during ontogenesis and development extends into postnatal period. Synchronized molecular oscillations develop earlier in the SCN than in the peripheral clocks. A hypothesis is suggested that the immature clocks might be first driven by external entraining cues, and therefore, serve as "slave" oscillators. During ontogenesis, the clocks may gradually develop a complete set of molecular interlocked oscillations, i.e., the molecular clockwork, and become self-sustained clocks.


2006 ◽  
Vol 23 (1-2) ◽  
pp. 307-315 ◽  
Author(s):  
Shinobu Yasuo ◽  
Miwa Watanabe ◽  
Masayuki Iigo ◽  
Takashi Yamamura ◽  
Nobuhiro Nakao ◽  
...  

1987 ◽  
Vol 2 (2) ◽  
pp. 139-152 ◽  
Author(s):  
Monica S. Saiovici ◽  
Trevor J. Nicholls ◽  
Brian K. Follett

1999 ◽  
Vol 14 (5) ◽  
pp. 378-390 ◽  
Author(s):  
Bora D. Zivkovic ◽  
Herbert Underwood ◽  
Christopher T. Steele ◽  
Kent Edmonds

1982 ◽  
Vol 242 (1) ◽  
pp. R44-R50 ◽  
Author(s):  
G. B. Ellis ◽  
R. E. McKlveen ◽  
F. W. Turek

We compared the effects of light pulses in constant darkness (DD) and dark pulses in constant light (LL) on the free-running rhythm of locomotor activity in male golden hamsters. Light pulses yielded advances, delays, or no change in the rhythm of activity. These data conform to a typical phase-response curve; this curve was unaffected by pinealectomy. Dark pulses occurring either late in the subjective night or early in the subjective day had little effect. In contrast, dark pulses occurring either late in the subjective day or early in the subjective night altered the rhythm in one of three ways: advance of the rhythm; splitting into two components; or induction of a new component, in phase with the pulse. Because dark pulses in LL perturb the circadian system in a different manner than do light pulses in DD, they may have value in identifying heretofore unknown aspects of circadian systems. As such, the use of dark pulses to perturb circadian rhythmicity will be a useful tool in examining the formal properties of circadian systems.


Sign in / Sign up

Export Citation Format

Share Document