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Neurons in the suprachiasmatic nucleus (SCN) generate circadian changes in the rates of spontaneous action potential firing that regulate and synchronize daily rhythms in physiology and behavior. Considerable evidence suggests that daily rhythms in the repetitive firing rates (higher during the day than at night) of SCN neurons are mediated by changes in subthreshold potassium (K) conductance(s). An alternative "bicycle" model for circadian regulation of membrane excitability in clock neurons, however, suggests that an increase in NALCN-encoded sodium (Na) leak conductance underlies daytime increases in firing rates. The experiments reported here explored the role of Na leak currents in regulating daytime and nighttime repetitive firing rates in identified adult male and female mouse SCN neurons: vasoactive intestinal peptide-expressing (VIP), neuromedin S-expressing (NMS) and gastrin-releasing peptide-expressing (GRP) cells. Whole-cell recordings from VIP, NMS, and GRP neurons in acute SCN slices revealed that Na leak current amplitudes/densities are similar during the day and at night, but have a larger impact on membrane potentials in daytime neurons. Additional experiments, using an conditional knockout approach, demonstrated that NALCN-encoded Na currents selectively regulate daytime repetitive firing rates of adult SCN neurons. Dynamic clamp-mediated manipulation revealed that the effects of NALCN-encoded Na currents on the repetitive firing rates of SCN neurons depend on K current-driven changes in input resistances. Together, these findings demonstrate that NALCN-encoded Na leak channels contribute to regulating daily rhythms in the excitability of SCN neurons by a mechanism that depends on K current-mediated rhythmic changes in intrinsic membrane properties. Elucidating the ionic mechanisms responsible for generating daily rhythms in the rates of spontaneous action potential firing of neurons in the suprachiasmatic nucleus (SCN), the master circadian pacemaker in mammals, is an important step toward understanding how the molecular clock controls circadian rhythms in physiology and behavior. While numerous studies have focused on identifying subthreshold K channel(s) that mediate day-night changes in the firing rates of SCN neurons, a role for Na leak currents has also been suggested. The results of the experiments presented here demonstrate that NALCN-encoded Na leak currents differentially modulate daily rhythms in the daytime/nighttime repetitive firing rates of SCN neurons as a consequence of rhythmic changes in subthreshold K currents.
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http://dx.doi.org/10.1523/JNEUROSCI.0182-23.2023 | DOI Listing |
Cell Rep
September 2025
Center for Hypothalamic Research, Department of Internal Medicine, UT Southwestern Medical Center, Dallas, TX, USA; Peter O'Donnell Jr. Brain Institute, UT Southwestern Medical Center, Dallas, TX, USA; Division of Endocrinology & Metabolism, Department of Internal Medicine, UT Southwestern Medical C
Food consumption impacts body weight differently depending on the time of day. Here, we investigated whether suprachiasmatic nucleus (SCN) neurons responsive to the hormone ghrelin temporally regulate eating and body weight in mice. The chemogenetic stimulation of GHSR (growth hormone secretagogue receptor)-expressing SCN neurons during the mid-rest phase-when mice are most sensitive to ghrelin's orexigenic effects-increased food intake.
View Article and Find Full Text PDFMolecules
August 2025
Faculty of Medicine, Institute for Anatomy II, Goethe University Frankfurt, Frankfurt am Main 60590, Germany.
Background: Signaling pathways like those depending on cAMP/PKA, calcium/calmodulin/CaMK, MEK-1/MAPK or PI3K/Akt have been described to modulate suprachiasmatic nucleus (SCN) neuronal signaling via influencing transcription factors like CREB. Here, we analyzed the effect of cyclic nucleotide phosphodiesterase inhibitors and structurally similar substances commonly used as autophagy modulators on a cell line stably expressing a cyclic nucleotide element-driven luciferase reporter.
Methods: We used an SCN cell line stably transfected with a CRE-luciferase reporter (SCNCRE) to evaluate signaling and vitality responses to various isoform-selective PDE inhibitors and autophagy modulators to evaluate the mechanism of action of the latter.
bioRxiv
July 2025
Department of Molecular, Cell and Cancer Biology, University of Massachusetts Chan Medical School, Worcester, MA 01605.
Energy homeostasis in mice is maintained through coordinated activity among hypothalamic nuclei that regulate food intake and thermogenesis. These processes must adapt to the sleep-wake cycle, yet the underlying pathways, cell types, and molecular mechanisms governing their diurnal regulation remain poorly understood. We show that mice lacking the E3 ubiquitin ligase are lean and resistant to diet-induced obesity, owing to reduced food intake and enhanced brown adipose tissue (BAT) thermogenesis.
View Article and Find Full Text PDFbioRxiv
July 2025
Champalimaud Centre for the Unknown, Lisbon, Portugal.
Neural computations support stable behavior despite relying on many dynamically changing biological processes. One such process is representational drift (RD), in which neurons' responses change over the timescale of minutes to weeks, while perception and behavior remain unchanged. Generally, RD is believed to be caused by changes in synaptic weights, which alter individual neurons' tuning properties.
View Article and Find Full Text PDFFront Physiol
July 2025
Department of Clinical Biochemistry, Copenhagen University Hospital - Bispebjerg and Frederiksberg, Copenhagen, Denmark.
Introduction: Prokineticin 2 (PK2) is believed to function as an output molecule, relaying circadian rhythms of behavior and physiology from the suprachiasmatic nucleus (SCN). The expression of PK2 in the SCN is primarily driven by the molecular clock, oscillating with high levels early-mid day and low levels during night. Furthermore, light at night induces the expression of PK2.
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