» Articles » PMID: 37833408

Neurovirulent Cytokines Increase Neuronal Excitability in a Model of Coronavirus-induced Neuroinflammation

Overview
Specialty Critical Care
Date 2023 Oct 13
PMID 37833408
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Neurological manifestations of severe coronavirus infections, including SARS-CoV-2, are wide-ranging and may persist following virus clearance. Detailed understanding of the underlying changes in brain function may facilitate the identification of therapeutic targets. We directly tested how neocortical function is impacted by the specific panel of cytokines that occur in coronavirus brain infection. Using the whole-cell patch-clamp technique, we determined how the five cytokines (TNFα, IL-1β, IL-6, IL-12p40 and IL-15 for 22-28-h) at concentrations matched to those elicited by MHV-A59 coronavirus brain infection, affected neuronal function in cultured primary mouse neocortical neurons.

Results: We evaluated how acute cytokine exposure affected neuronal excitability (propensity to fire action potentials), membrane properties, and action potential characteristics, as well as sensitivity to changes in extracellular calcium and magnesium (divalent) concentration. Neurovirulent cytokines increased spontaneous excitability and response to low divalent concentration by depolarizing the resting membrane potential and hyperpolarizing the action potential threshold. Evoked excitability was also enhanced by neurovirulent cytokines at physiological divalent concentrations. At low divalent concentrations, the change in evoked excitability was attenuated. One hour after cytokine removal, spontaneous excitability and hyperpolarization of the action potential threshold normalized but membrane depolarization and attenuated divalent-dependent excitability persisted.

Conclusions: Coronavirus-associated cytokine exposure increases spontaneous excitability in neocortical neurons, and some of the changes persist after cytokine removal.

References
1.
Koller H, Siebler M, Schmalenbach C, Muller H . GABA and glutamate receptor development of cultured neurons from rat hippocampus, septal region, and neocortex. Synapse. 1990; 5(1):59-64. DOI: 10.1002/syn.890050105. View

2.
Jones B, Smith S . Calcium-Sensing Receptor: A Key Target for Extracellular Calcium Signaling in Neurons. Front Physiol. 2016; 7:116. PMC: 4811949. DOI: 10.3389/fphys.2016.00116. View

3.
Heir R, Stellwagen D . TNF-Mediated Homeostatic Synaptic Plasticity: From to Models. Front Cell Neurosci. 2020; 14:565841. PMC: 7556297. DOI: 10.3389/fncel.2020.565841. View

4.
Yang Z, Du J, Chen G, Zhao J, Yang X, Su L . Coronavirus MHV-A59 infects the lung and causes severe pneumonia in C57BL/6 mice. Virol Sin. 2014; 29(6):393-402. PMC: 7090691. DOI: 10.1007/s12250-014-3530-y. View

5.
Wouk J, Rechenchoski D, Rodrigues B, Ribelato E, Faccin-Galhardi L . Viral infections and their relationship to neurological disorders. Arch Virol. 2021; 166(3):733-753. PMC: 7838016. DOI: 10.1007/s00705-021-04959-6. View