Daily variation of muscarinic receptors in visual cortex but not suprachiasmatic nucleus of Syrian hamsters

K. G. Bina, B. Rusak, M. Wilkinson

Research output: Contribution to journalArticlepeer-review

19 Citations (Scopus)

Abstract

Intraventricular administration of carbachol can induce phase shifts in wheel-running activity in rodents, which depend on circadian phase and are mediated via muscarinic cholinergic receptors in Syrian hamsters. We studied the circadian variation in binding of 3H]-N-methylscopolamine ([3H]NMS), a hydrophilic muscarinic receptor antagonist, in micropunches obtained from the anterior hypothalamus and occipital cortex of Syrian hamsters housed in a 14:10 light:dark cycle. Binding sites were characterized on cells contained within 1 mm punches (obtained from slices 300 μm thick), using a method to selectively detect cell surface (functional) receptors. Atropine sulphate was used to determine nonspecific binding. Cortex showed a significant daily rhythm in [3H]NMS binding with a peak occurring late in the light phase and a trough at lights on, while the hypothalamus showed no detectable rhythm. Following suprachiasmatic nucleus (SCN) ablation or maintenance in constant darkness, the rhythm in the cortex was abolished. These findings suggest that photic information conveyed via the SCN is responsible for the receptor binding rhythm in the cortex. Autoradiographic studies ([3H]NMS; 2 nM, 3 weeks exposure) clearly revealed both M1 and M2 subtypes of muscarinic receptors in the region of the SCN and the visual cortex.

Original languageEnglish
Pages (from-to)143-153
Number of pages11
JournalBrain Research
Volume797
Issue number1
DOIs
Publication statusPublished - Jun 22 1998

Bibliographical note

Funding Information:
This research was supported by grants to BR from the US AFOSR (F49620-96-1-0038) and NSERC of Canada (A0305) and to MW from the MRC of Canada (MT-7131). This study was included as part of a dissertation submitted in partial fulfillment of the requirements for a PhD degree at Dalhousie University. We are indebted to D. Goguen and H. Grant for their technical assistance, to Dr. K. Semba for comments on an earlier version of the manuscript and to J. Baker for secretarial assistance.

ASJC Scopus Subject Areas

  • General Neuroscience
  • Molecular Biology
  • Clinical Neurology
  • Developmental Biology

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