Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1978 Dec;75(12):6276–6280. doi: 10.1073/pnas.75.12.6276

"Dark-active" rat transformed into "light-active" rat by destruction of 24-hr clock: function of 24-hr clock and synchronizers.

C P Richter
PMCID: PMC393164  PMID: 282645

Abstract

In alternating 12-hr periods of light and dark the rat is active mainly in the dark. Its activity in the dark (beginning at 1800) depends exclusively on release of activity by the 24-hr clock. In the light (beginning at 0600) the 24-hr clock inhibits activity; the normal rat becomes totally inactive in the light except for activity resulting from external stimulation. After section of the connections between the optic chiasma and the hypothalamus, some rats become totally and permanently inactive in the dark. This sectioning destroys the 24-hr clock. After destruction of the clock removes inhibition of activity in the light period, the rat becomes active promptly at start of the light period--i.e., becomes a "light-active" animal. In the normal rat, activity becomes synchronized to start of the dark (by the electric clock at 1800), regardless of the amounts of activity. Destruction of the 24-hr clock eliminates the synchronizer at 1800. However, almost at once, activity, eating, and drinking are kept together by a second synchronizer, start of the light (by the electric clock at 0600). This may explain the ability of the rat to survive after destruction of the 24-hr clock.

Full text

PDF
6276

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Fuller C. A., Sulzman F. M., Moore-Ede M. C. Thermoregulation is impaired in an environment without circadian time cues. Science. 1978 Feb 17;199(4330):794–796. doi: 10.1126/science.414356. [DOI] [PubMed] [Google Scholar]
  2. Moore-ede M. C., Schmelzer W. S., Kass D. A., Herd J. A. Cortisol-mediated synchrinization of circadian rhythm in urinary potassium excretion. Am J Physiol. 1977 Nov;233(5):R230–R238. doi: 10.1152/ajpregu.1977.233.5.R230. [DOI] [PubMed] [Google Scholar]
  3. Richter C. P. BIOLOGICAL CLOCKS IN MEDICINE AND PSYCHIATRY: SHOCK-PHASE HYPOTHESIS. Proc Natl Acad Sci U S A. 1960 Nov;46(11):1506–1530. doi: 10.1073/pnas.46.11.1506. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Richter C. P. Discovery of fire by man--its effects on his 24-hour clock and intellectual and cultural evolution. Johns Hopkins Med J. 1977 Aug;141(2):47–61. [PubMed] [Google Scholar]
  5. Richter C. P. Sleep and activity: their relation to the 24-hour clock. Res Publ Assoc Res Nerv Ment Dis. 1967;45:8–29. [PubMed] [Google Scholar]
  6. Richter C. P., Warner C. L. Comparison of Weigert stained sections with unfixed, unstained sections for study of myelin sheaths. Proc Natl Acad Sci U S A. 1974 Mar;71(3):598–601. doi: 10.1073/pnas.71.3.598. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. STELLAR E., HILL J. H. The rats rate of drinking as a function of water deprivation. J Comp Physiol Psychol. 1952 Feb;45(1):96–102. doi: 10.1037/h0062150. [DOI] [PubMed] [Google Scholar]
  8. Stetson M. H., Watson-Whitmyre M. Nucleus suprachiasmaticus: the biological clock in the hamster? Science. 1976 Jan 16;191(4223):197–199. doi: 10.1126/science.942799. [DOI] [PubMed] [Google Scholar]
  9. Sulzman F. M., Fuller C. A., Moore-Ede M. C. Comparison of synchronization of primate circadian rhythms by light and food. Am J Physiol. 1978 Mar;234(3):R130–R135. doi: 10.1152/ajpregu.1978.234.3.R130. [DOI] [PubMed] [Google Scholar]
  10. de GROOT The rat hypothalamus in stereotaxic coordinates. J Comp Neurol. 1959 Dec;113:389–400. doi: 10.1002/cne.901130304. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES