# Mapping the linkage between auricular vagus nerve receptors and cardiovagal modulation

> **NIH NIH OT2** · MASSACHUSETTS GENERAL HOSPITAL · 2021 · $273,894

## Abstract

The vagus nerve is regarded as the main parasympathetic conduit of the autonomic nervous system and is
involved in the regulation of heart rate, cardiac contractility, ventricular electrical stability and baroreflex
sensitivity. Vagus nerve stimulation (VNS) has been suggested and/or used as a neuromodulatory therapy for
multiple cardiovascular disorders, including hypertension, coronary artery disease, and heart failure. However,
given that VNS is an invasive procedure and has been associated with significant adverse events, the mapping
of alternative non-invasive pathways for vagal modulation is of critical relevance. Interestingly, the auricular
branch of the vagus (ABVN) is the only peripheral branch of this nerve that distributes to the skin. Previous
animal studies have demonstrated that ABVN sensory fibers terminate in the nucleus tractus solitarius (NTS),
and, similar to invasive VNS, ABVN stimulation has also been shown to modulate cardiac electrophysiology
resulting in atrial fibrillation suppression, and regulation of left ventricular remodeling. While the anatomy of this
nerve has been studied in detail, the functional mapping of the circuitry connecting ABVN stimulation with
cardiovascular outcomes remains poorly understood. Moreover, as NTS activity and the dorsal medullary vagal
system operates in tune with respiration, our group has previously suggested that the neuromodulatory effects
of ABVN afference can be optimized by gating stimulation to the respiratory cycle. Hence, our overall goal is to
functionally map the ABVN-brainstem-cardiovagal outflow pathway in both humans and rodents and assess its
sensitivity to the modulatory effects of respiration. In humans, state-of-the-art ultrahigh-field functional MRI (7T
fMRI) will afford enhanced spatiotemporal resolution to evaluate the response of the dorsal medullary vagal
system and hypothalamus to ABVN stimulation. Neuroimaging will incorporate simultaneous
cardiophysiological assessment and dynamic high frequency heart rate variability (HF-HRV) assessment of
cardiovagal modulation, using advanced point-process adaptive filtering algorithms developed by our group.
More invasive experiments in a rat model will evaluate the effects of ABVN afference on cervical vagus nerve
activity (CVNA), while electrocardiography will be recorded to calculate HF-HRV response to ABVN
stimulation, thereby directly linking unique rat and human outcomes via a metric common to both. Rat studies
will also assess activation in brainstem and hypothalamic homologue nuclei by c-Fos immunohistochemistry in
the absence and presence of neuronal activity blocker, and excitatory and inhibitory neurotransmitter
antagonists injected stereotactically into the target nuclei. In summary, the functional mapping of the ABVN
pathway in humans is of pivotal importance given its accessibility and its potential neuromodulatory effects on
cardiovascular physiology, and our proposal will significantly improve our understandi...

## Key facts

- **NIH application ID:** 10357723
- **Project number:** 3OT2OD023867-01S6
- **Recipient organization:** MASSACHUSETTS GENERAL HOSPITAL
- **Principal Investigator:** VITALY NAPADOW
- **Activity code:** OT2 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2021
- **Award amount:** $273,894
- **Award type:** 3
- **Project period:** 2016-09-28 → 2022-11-30

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10357723

## Citation

> US National Institutes of Health, RePORTER application 10357723, Mapping the linkage between auricular vagus nerve receptors and cardiovagal modulation (3OT2OD023867-01S6). Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/grant/nih/10357723. Licensed CC0.

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