Skip to main content
Log in

Effects of bilateral suprachiasmatic nucleus lesions on the circadian rhythms in a diurnal rodent, the Siberian chipmunk (Eutamias sibiricus)

  • Published:
Journal of Comparative Physiology A Aims and scope Submit manuscript

Summary

Effects of bilateral SCN lesions on the circadian rhythms of wheel-running activity and sleep-waking were examined in a diurnal rodent, the Siberian chipmunk,Eutamias sibiricus. The following results suggest that the SCN is a circadian pacemaker in the Siberian chipmunk:

  1. 1.

    Retinohypothalamic projection was established in the chipmunk using HRP as an anterograde tracer (Fig. 1). The projection was bilateral and greater to the contralateral SCN. Unlike in the rat, axon terminals were distributed through-out the dorsoventral extent of the SCN.

  2. 2.

    Complete bilateral lesions of the SCN resulted in disruption of the circadian rhythmicity in wheel-running activity (Fig. 2 and Table 1) under dim constant light (LL) (n=4) and in blinded chipmunks (n=2). Daily rhythms under light-dark (LD) were also abolished (n=3). The animals with incomplete SCN lesions (n=5) reestablished circadian rhythmicity (Fig. 3). Significant shortening of the freerunning period was observed in two cases. In the other three cases, circadian rhythmicity was unstable and the period of the rhythms was variable.

  3. 3.

    Disruption of the circadian rhythm after total SCN lesions was also reflected in the hourly proportion of SWS, PS, and W (Fig. 5 and Table 2,n=4).

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

SCN :

suprachiasmatic nucleus

W :

waking

SWS :

slow-wave sleep

PS :

paradoxical sleep

HRP :

horseradish peroxidase

References

  • Davis FC, Gorski RA (1984) Unilateral lesions of the hamster suprachiasmatic nuclei: evidence for redundant control of circadian rhythms. J Comp Physiol A 154:221–232

    Google Scholar 

  • Green DJ, Gillette R (1982) Circadian rhythm of firing rate recorded from single cells in the rat suprachiasmatic brain slice. Brain Res 245:198–200

    Google Scholar 

  • Groos G, Hendriks J (1982) Circadian rhythms in electrical discharge of rat suprachiasmatic neurons recorded in vitro. Neurosci Lett 34:283–288

    Google Scholar 

  • Ibuka N, Kawamura H (1975) Loss of circadian sleep-wakefulness cycle in the rat by suprachiasmatic nucleus lesions. Brain Res 96:76–81

    Google Scholar 

  • Ibuka N, Inouye ST, Kawamura H (1977) Analysis of sleep-wakefulness rhythms in male rats after suprachiasmatic nucleus lesions and ocular enucleation. Brain Res 122:33–47

    Google Scholar 

  • Ibuka N, Nihonmatsu I, Sekiguchi S (1980) Sleep-wakefulness rhythms in mice after suprachiasmatic nucleus lesions. Waking Sleeping 4:167–173

    Google Scholar 

  • Inouye ST, Kawamura H (1979) Persistence of circadian rhythmicity in mammalian hypothalamic ‘island’ containing the suprachiasmatic nucleus. Proc Natl Acad Sci USA 76:5962–5966

    Google Scholar 

  • Inouye ST, Kawamura H (1982) Characteristics of a circadian pacemaker in the suprachiasmatic nucleus. J Comp Physiol 146:153–160

    Google Scholar 

  • Kawamura H, Inouye ST (1979) Circadian rhythm in a hypothalamic island containing the suprachiasmatic nucleus. In: Suda M, Hayaishi O, Nakagawa H (eds) Biological rhythms and their central mechanism. Elsevier/North Holland Biomedical Press, Amsterdam, pp 335–341

    Google Scholar 

  • Mesulam MM (1978) Tetramethylbenzidine for horseradish peroxidase neurohistochemistry: A non-carcinogenic blue reaction product with superior sensitivity for visualizing neural afferents and efferents. J Histochem Cytochem 26:106–117

    Google Scholar 

  • Moore RY (1973) Retinohypothalamic projection in mammals: A comparative study. Brain Res 49:403–409

    Google Scholar 

  • Moore RY (1983) Organization and function of a central nervous system circadian oscillator: The suprachiasmatic hypothalamic nucleus. Fed Proc 42:2783–2789

    Google Scholar 

  • Moore RY, Eichler VB (1972) Loss of a circadian adrenal corticosterone rhythm following suprachiasmatic lesions in the rat. Brain Res 42:201–206

    Google Scholar 

  • Pickard GE, Silverman AJ (1981) Direct retinal projections to the hypothalamus, piriform cortex and accessory optic nuclei in the golden hamster as demonstrated by a sensitive anterograde horseradish peroxidase technique. J Comp Neurol 196:155–172

    Google Scholar 

  • Pohl H (1972) Die Aktivitätsperiodik von zwei tagaktiven Nagern,Funambulus palmarum undEutamias sibiricus unter Dauerlichtbedingungen. J Comp Physiol 78:60–74

    Google Scholar 

  • Richter CP (1978a) Evidence for existence of a yearly clock in surgically and self-blinded chipmunks. Proc Natl Acad Sci USA 75:3517–3521

    Google Scholar 

  • Richter CP (1978b) ‘Dark-active’ rat transformed into ‘light-active’ rat by destruction of 24-hr clock: Function of 24-hr clock and synchronizers. Proc Natl Acad Sci USA 75:6276–6280

    Google Scholar 

  • Rusak B (1977) The role of the suprachiasmatic nuclei in the generation of circadian rhythms in the golden hamster,Mesocricetus auratus. J Comp Physiol 118:145–164

    Google Scholar 

  • Rusak B, Groos G (1982) Suprachiasmatic stimulation phase shifts rodent circadian rhythms. Science 215:1407–1409

    Google Scholar 

  • Rusak B, Zucker I (1979) Neural regulation of circadian rhythms. Physiol Rev 59:449–526

    Google Scholar 

  • Sato T, Kawamura H (1984) Circadian rhythms in multiple unit activity inside and outside the suprachiasmatic nucleus in the diurnal chipmunk (Eutamias sibiricus) Neurosci Res 1:45–52

    Google Scholar 

  • Sato T, Nihonmatsu I, Kawamura H (1983) Central mechanisms of circadian rhythms in the chipmunk. Neurosci Lett Suppl 13:830

    Google Scholar 

  • Sawaki Y, Nihonmatsu I, Kawamura H (1984) Transplantation of the neonatal suprachiasmatic nuclei into rats with complete bilateral suprachiasmatic lesions. Neurosci Res 1:67–72

    Google Scholar 

  • Schwartz WJ, Gainer H (1977) Suprachiasmatic nucleus: Use of14C-labeled deoxyglucose uptake as a functional marker. Science 197:1089–1091

    Google Scholar 

  • Schwartz WJ, Davidsen LC, Smith CB (1980) In vivo metabolic activity of a putative circadian oscillator, the rat suprachiasmatic nucleus. J Comp Neurol 189:157–167

    Google Scholar 

  • Shibata S, Oomura Y, Kita H, Hattori K (1982) Circadian rhythmic changes of neuronal activity in the suprachiasmatic nucleus of the rat hypothalamic slice. Brain Res 247:154–158

    Google Scholar 

  • Stephan FK, Zucker I (1972) Circadian rhythms in drinking behavior and locomotor ativity of rats are eliminated by hypothalamic lesions. Proc Natl Acad Sci USA 69:1583–1586

    Google Scholar 

  • Stetson MH, Watson-Whitmyre M (1976) Nucleus suprachiasmaticus: The biological clock in the hamster? Science 191:197–199

    Google Scholar 

  • Takahashi JS, Menaker M (1982) Role of the suprachiasmatic nuclei in the circadian system of the house sparrow,Passer domesticus. J Neurosci 6:815–828

    Google Scholar 

  • Zucker I, Bosches M, Dark J (1983) Suprachiasmatic nuclei influence circannual and circadian rhythms of ground squirrels. Am J Physiol 244:R472-R480

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Sato, T., Kawamura, H. Effects of bilateral suprachiasmatic nucleus lesions on the circadian rhythms in a diurnal rodent, the Siberian chipmunk (Eutamias sibiricus). J. Comp. Physiol. 155, 745–752 (1984). https://doi.org/10.1007/BF00611591

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00611591

Keywords

Navigation