Daily changes in neuronal activities of the dorsal motor nucleus of the vagus under standard and short-term high fat diet – implications for circadian modulation of parasympathetic outflow

Author:

Chrobok LukaszORCID,Klich Jasmin DORCID,Jeczmien-Lazur Jagoda SORCID,Pradel KamilORCID,Palus-Chramiec KatarzynaORCID,Sanetra Anna MORCID,Piggins Hugh DORCID,Lewandowski Marian HORCID

Abstract

ABSTRACTThe suprachiasmatic nuclei (SCN) of the hypothalamus functions as the brain’s primary circadian clock, but circadian clock genes are also rhythmically expressed in several extra-SCN brain sites where they can exert local temporal control over physiology and behaviour. Recently, we found that the hindbrain dorsal vagal complex possesses strong daily timekeeping capabilities, with the area postrema and nucleus of the solitary tract exhibiting the most robust clock properties. The possibility that the executory part of this complex – the dorsal motor nucleus of the vagus (DMV), also exhibits daily changes has not been extensively studied. The DMV is the source of vagal efferent motoneurons largely responsible for the regulation of gastric motility and emptying and consequently influence meal size and energy homeostasis. We used a combination of multi-channel electrophysiology and patch clamp recordings to gain insight into possible daily variation in these DMV cells and how this is influenced by diet. We found that DMV neurons increase their spontaneous activity, excitability and responsiveness to metabolic neuromodulators at late day which was paralleled with an enhanced synaptic input to these neurons. A high-fat diet typically damps circadian rhythms, but we found that short-term exposure to a high-fat diet paradoxically amplified daily variation of DMV neuronal activity, while blunting their responsiveness to metabolic neuromodulators. In summary, we show for the first time that neural activity at a source of vagal efferents varies with time of day and that this temporal variation is modulated by diet. These findings have clear implications for our understanding of the daily control of parasympathetic outflow.

Publisher

Cold Spring Harbor Laboratory

Reference60 articles.

1. Glucagon-Like Peptide 1 Excites Hypocretin/Orexin Neurons by Direct and Indirect Mechanisms: Implications for Viscera-Mediated Arousal

2. Ionic Channel Function in Action Potential Generation: Current Perspective

3. Circadian misalignment and health

4. Baron KG & Reid KJ (2015). Relationship between Circadian Rhythms, Feeding, and Obesity. In Modulation of Sleep by Obesity, Diabetes, Age, and Diet, pp. 243–253. Elsevier. Available at: https://linkinghub.elsevier.com/retrieve/pii/B9780124201682000260.

5. Belle MDC , Baño-Otalora B & Piggins HD (2021). Perforated Multi-Electrode Array Recording in Hypothalamic Brain Slices. In Methods in molecular biology (Clifton, N.J.), pp. 263–285. Available at: http://www.ncbi.nlm.nih.gov/pubmed/33284451.

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