Vagus nerve stimulation (VNS) is a promising application of bioelectronic medicine to treat many pathologies, ranging from epilepsy and depression to cardiovascular diseases. Conventional VNS is not optimized taking into account the topographic organization of the vagus nerve, resulting in suboptimal stimulation protocols, which can lead to severe adverse effects. The development of in vivo methods to determine topographic organization would allow more selective stimulation protocols and is thus pivotal in the development of future therapies. Here, we show that it may be possible to reverse-engineer vagus nerve topographic organization starting from experimental evoked compound action potentials (ECAPs). The parameters of a biophysical model of ECAP generation are varied until the optimal matching between synthetic and experimental ECAPs is determined. In the present work, we managed to match an experimental ECAP obtained from swine VNS, and to replicate the shape of an unseen experimental ECAP through the optimized parameters. This work paves the way to the automatic optimization of selective VNS protocols, opening to new important therapeutic opportunities.
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http://dx.doi.org/10.1109/EMBC53108.2024.10781787 | DOI Listing |
Front Physiol
February 2025
TNO Human Performance, Soesterberg, Netherlands.
Introduction: Maintaining cognitive performance during sleep deprivation is of vital importance in many professions, especially in high-risk professions like the military. It has long been known that sleep deprivation diminishes cognitive performance. To mitigate the negative effects on cognitive performance during crucial military tasks, new interventions are necessary.
View Article and Find Full Text PDFJ Physiol
March 2025
Department of Physiology and Pharmacology, SUNY Downstate Health Sciences University, Brooklyn, NY, USA.
The intrinsic cardiac nervous system (ICNS), termed as the heart's 'little brain', is the final point of neural regulation of cardiac function. Studying the dynamic behaviour of these ICNS neurons via multiscale neuronal computer models has been limited by the sparsity of electrophysiological data. We developed and analysed a computational library of neuronal electrophysiological models based on single neuron transcriptomic data obtained from ICNS neurons.
View Article and Find Full Text PDFInt J Mol Sci
February 2025
Department of Physiology and Biophysics, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte 31270-901, Brazil.
The liver serves as a major energetic reservoir for other tissues and its metabolic function is controlled by humoral and neural factors. The vagus nerve innervating the gastrointestinal tract plays an important role in regulating peripheral metabolism and energy expenditure. Although the liver receives vagus nerve fibers, the impact of this circuitry in the regulation of hepatic metabolism is still poorly understood.
View Article and Find Full Text PDFInt J Mol Sci
February 2025
Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, DK-2100 Copenhagen, Denmark.
Afferent vagal neurons convey gut-brain signals related to the mechanical and chemical sensing of nutrients, with the latter also mediated by gut hormones secreted from enteroendocrine cells. Cell bodies of these neurons are located in the nodose ganglia (NG), with the right NG playing a key role in metabolic regulation. Notably, glucagon-like peptide-1 receptor (GLP1R) neurons primarily innervate the muscle layer of the stomach, distant from glucagon-like peptide-1 (GLP-1)-secreting gut cells.
View Article and Find Full Text PDFEur J Med Res
March 2025
Department of Anesthesiology, Jincheng People's Hospital, 1666 Baishui East Street, Jincheng, 048026, Shanxi, China.
Background: Vagus nerve stimulation (VNS) exhibits protective effects against remote organ injury following ischemia-reperfusion (I/R). However, its effects on acute myocardial injury induced by hepatic I/R in rats, and the underlying mechanisms, remain unclear.
Methods: Thirty male rats were randomly assigned to five groups: Sham, I/R, VNS, VNS + Erastin, and VNS + DMSO.
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