Evidence map›Paper›PMID 34416255›Full record

ArticleBrain research2021

Dedicated C-fiber vagal sensory afferent pathways to the paraventricular nucleus of the hypothalamus.

Jessica A Fawley, Deborah M Hegarty, Sue A Aicher, Eric Beaumont, Michael C Andresen

Open access · greenAbstract read
In one paragraph

Article in Brain research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. CCK-expressing neurons in the NTS are directly activated by CCK-sensitive C-type vagal afferents.American journal of physiology. Regulatory, integrative and comparative physiology · 2025
    Article
  7. Review
  8. Neural circuits regulating visceral pain.Communications biology · 2024
    Review
  9. The Coding Logic of Interoception.Annual review of physiology · 2024
    Review
  10. Article
  11. Neural control of the spleen as an effector of immune responses to inflammation: mechanisms and treatments.American journal of physiology. Regulatory, integrative and comparative physiology · 2022
    Review
  12. Article
  13. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Jessica A FawleyDepartment of Chemical Physiology & Biochemistry, Oregon Health & Science University, Portland, OR 97239, United States.
Deborah M HegartyDepartment of Chemical Physiology & Biochemistry, Oregon Health & Science University, Portland, OR 97239, United States.
Sue A AicherDepartment of Chemical Physiology & Biochemistry, Oregon Health & Science University, Portland, OR 97239, United States.
Eric BeaumontDepartment of Biomedical Sciences, Quillen College of Medicine, East Tennessee State University, Johnson City, TN 37614, United States.
Michael C AndresenDepartment of Chemical Physiology & Biochemistry, Oregon Health & Science University, Portland, OR 97239, United States. Electronic address: andresen@ohsu.edu.
Oregon Health & Science University · USEast Tennessee State University · US

Funding

Afferent Mechanisms of Vagal Neuromodulation TherapyR01HL141560 · NHLBI · EAST TENNESSEE STATE UNIVERSITY · PI Eric Beaumont · 2018 to 2026
$4.5M
Lipid signaling in cardiovascular afferent transmissionR01HL133505 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI ANDRESEN, MICHAEL CHRISTIAN · 2016 to 2019
$1.8M
NHLBI NIH HHS R01 HL133505NHLBI NIH HHS R01 HL141560
6 · The paper itself

Abstract

The nucleus of the solitary tract (NTS) receives viscerosensory information from the vagus nerve to regulate diverse homeostatic reflex functions. The NTS projects to a wide network of other brain regions, including the paraventricular nucleus of the hypothalamus (PVN). Here we examined the synaptic characteristics of primary afferent pathways to PVN-projecting NTS neurons in rat brainstem slices.Expression of the Transient Receptor Potential Vanilloid receptor (TRPV1+ ) distinguishes C-fiber afferents within the solitary tract (ST) from A-fibers (TRPV1-). We used resiniferatoxin (RTX), a TRPV1 agonist, to differentiate the two. The variability in the latency (jitter) of evoked excitatory postsynaptic currents (ST-EPSCs) distinguished monosynaptic from polysynaptic ST-EPSCs. Rhodamine injected into PVN was retrogradely transported to identify PVN-projecting NTS neurons within brainstem slices. Graded shocks to the ST elicited all-or-none EPSCs in rhodamine-positive NTS neurons with latencies that had either low jitter (<200 µs - monosynaptic), high jitter (>200 µs - polysynaptic inputs) or both. RTX blocked ST-evoked TRPV1 + EPSCs whether mono- or polysynaptic. Most PVN-projecting NTS neurons (17/21 neurons) had at least one input polysynaptically connected to the ST. Compared to unlabeled NTS neurons, PVN-projecting NTS neurons were more likely to receive indirect inputs and be higher order. Surprisingly, sEPSC rates for PVN-projecting neurons were double that of unlabeled NTS neurons. The ST synaptic responses for PVN-projecting NTS neurons were either all TRPV1+ or all TRPV1-, including neurons that received both direct and indirect inputs. Overall, PVN-projecting NTS neurons received direct and indirect vagal afferent information with strict segregation regarding TRPV1 expression.

Indexed as

Afferent PathwaysAnimalsDiterpenesExcitatory Postsynaptic PotentialsMaleNerve Fibers, UnmyelinatedParaventricular Hypothalamic NucleusPatch-Clamp TechniquesRatsRats, Sprague-DawleySolitary NucleusSynapsesTRPV Cation ChannelsVagus NerveDiterpenesresiniferatoxinTrpv1 protein, ratTRPV Cation ChannelsHypothalamusParaventricular nucleusSolitary tract nucleusTRPV1Vagal afferent

Identifiers

PMID34416255
PMCPMC8438991
OpenAlexW3196098783

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.