Abstract

Cells of the dorsomedial/lateral hypothalamus (DMH/LH) that produce hypocretin (HCRT) promote arousal in part by activation of cells of the locus coeruleus (LC) which express tyrosine hydroxylase (TH). The suprachiasmatic nucleus (SCN) drives endogenous daily rhythms, including those of sleep and wakefulness. These circadian oscillations are generated by a transcriptional-translational feedback loop in which the Period (Per) genes constitute critical components. This cell-autonomous molecular clock operates not only within the SCN but also in neurons of other brain regions. However, the phenotype of such neurons and the nature of the phase controlling signal from the pacemaker are largely unknown. We used dual fluorescent in situ hybridization to assess clock function in vasopressin, HCRT and TH cells of the SCN, DMH/LH and LC, respectively, of male Syrian hamsters. In the first experiment, we found that Per1 expression in HCRT and TH oscillated in animals held in constant darkness with a peak phase that lagged that in AVP cells of the SCN by several hours. In the second experiment, hamsters induced to split their locomotor rhythms by exposure to constant light had asymmetric Per1 expression within cells of the middle SCN at 6 h before activity onset (AO) and in HCRT cells 9 h before and at AO. We did not observe evidence of lateralization of Per1 expression in the LC. We conclude that the SCN communicates circadian phase to HCRT cells via lateralized neural projections, and suggests that Per1 expression in the LC may be regulated by signals of a global or bilateral nature.

Highlights

  • Temporal coordination of mammalian physiology and behavior is maintained by the suprachiasmatic nucleus of the hypothalamus (SCN; [1])

  • Our first experiment was designed to determine whether clock genes are expressed in a circadian pattern within two arousal-promoting cell types, the hypocretin cells of the lateral/dorsomedial hypothalamus (LH/DMH) and the tyrosine hydroxylase (TH)-expressing cells of the locus coeruleus (LC)

  • Consistent with earlier reports, we found that LL exposure adequate to induce splitting of locomotor activity resulted in regionally and phenotypically specific asymmetry of Per1 expression in the SCN: within AVP cells colabeled with Per1 in the middle plane of the SCN, the ratio of high to low Per1 intensity was greater at 6 h before activity onset (AO) than at 9 h before AO (p,0.05; figure 3A) and greater than unsplit control (p,0.05)

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Summary

Introduction

Temporal coordination of mammalian physiology and behavior is maintained by the suprachiasmatic nucleus of the hypothalamus (SCN; [1]). Hypocretins produced exclusively in the perifornical dorsomedial hypothalamus act to promote wakefulness through ascending projections, and by exciting arousal-promoting midbrain regions, including the locus coeruleus [15,16,17,18,19,20]. The phenotype of some extra-SCN neuronal oscillators has been established [26,27,28,29,30,31,32], the expression of clock genes in neurons that regulate sleep and wakefulness is not established and their dependence upon the SCN pacemaker is unclear. Our first experiment was designed to determine whether clock genes are expressed in a circadian pattern within two arousal-promoting cell types, the hypocretin cells of the lateral/dorsomedial hypothalamus (LH/DMH) and the tyrosine hydroxylase (TH)-expressing cells of the locus coeruleus (LC)

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