High salt diet increases suprachiasmatic neuronal excitability through endothelin receptor type B signaling.

Abstract

Circadian rhythms are 24-hour oscillations in behavioral and biological processes such as blood pressure and sodium excretion. Endothelin receptor B (ETB) has been connected to the molecular clock in peripheral tissues and plays a key role in the regulation of sodium excretion, especially in response to a high salt diet. However, little is known about the role of ETB in the primary circadian pacemaker in the brain, the suprachiasmatic nucleus (SCN), despite recent reports showing its enrichment in SCN astrocytes. In this study, we tested the hypothesis that high salt diet (4.0% NaCl) impacts the circadian system via the ETB receptor at the behavioral, molecular and physiological levels in C57BL/6 mice. Two weeks of high salt diet feeding changed the organization of nighttime wheel-running activity, as well as increased SCN expression of ETB mRNA determined by fluorescence in situ hybridization at night. Neuronal excitability determined using loose-patch electrophysiology was also elevated at night. This high salt diet-induced increase in SCN activity was ameliorated by ex vivo bath application of an ETB antagonist and could be mimicked with acute treatment of endothelin-3. Finally, we found that the excitatory effects of endothelin-3 were blocked with co-application of an NMDA receptor antagonist, suggesting that glutamate mediates endothelin-induced neuronal excitability in the SCN. Together our data demonstrate the presence of functional ETB receptors in SCN astrocytes and point to a novel role for endothelin signaling in mediating neuronal responses to a dietary sodium intake.