Evidence map›Paper›PMID 36046221›Full record

ReviewFrontiers in synaptic neuroscience2022

Cellular basis of learning and memory in the carotid body.

Olivia M S Gold, Emma N Bardsley, Anna P Ponnampalam, Audrys G Pauza, Julian F R Paton

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in synaptic neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Targeting the Carotid Body Function With Big-KPharmacology research & perspectives · 2026
    Article
  2. Review
  3. Review
  4. Multi-Organ Denervation: The Past, Present and Future.Journal of clinical medicine · 2025
    Review
  5. Review
  6. 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 1 institution in 1 country.

Olivia M S GoldManaaki Manawa - The Center for Heart Research, Department of Physiology, Faculty of Health and Medical Sciences, University of Auckland, Auckland, New Zealand.
Emma N BardsleyManaaki Manawa - The Center for Heart Research, Department of Physiology, Faculty of Health and Medical Sciences, University of Auckland, Auckland, New Zealand.
Anna P PonnampalamManaaki Manawa - The Center for Heart Research, Department of Physiology, Faculty of Health and Medical Sciences, University of Auckland, Auckland, New Zealand.
Audrys G PauzaManaaki Manawa - The Center for Heart Research, Department of Physiology, Faculty of Health and Medical Sciences, University of Auckland, Auckland, New Zealand.
Julian F R PatonManaaki Manawa - The Center for Heart Research, Department of Physiology, Faculty of Health and Medical Sciences, University of Auckland, Auckland, New Zealand.
University of Auckland · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The carotid body is the primary peripheral chemoreceptor in the body, and critical for respiration and cardiovascular adjustments during hypoxia. Yet considerable evidence now implicates the carotid body as a multimodal sensor, mediating the chemoreflexes of a wide range of physiological responses, including pH, temperature, and acidosis as well as hormonal, glucose and immune regulation. How does the carotid body detect and initiate appropriate physiological responses for these diverse stimuli? The answer to this may lie in the structure of the carotid body itself. We suggest that at an organ-level the carotid body is comparable to a miniature brain with compartmentalized discrete regions of clustered glomus cells defined by their neurotransmitter expression and receptor profiles, and with connectivity to defined reflex arcs that play a key role in initiating distinct physiological responses, similar in many ways to a switchboard that connects specific inputs to selective outputs. Similarly, within the central nervous system, specific physiological outcomes are co-ordinated, through signaling via distinct neuronal connectivity. As with the brain, we propose that highly organized cellular connectivity is critical for mediating co-ordinated outputs from the carotid body to a given stimulus. Moreover, it appears that the rudimentary components for synaptic plasticity, and learning and memory are conserved in the carotid body including the presence of glutamate and GABAergic systems, where evidence pinpoints that pathophysiology of common diseases of the carotid body may be linked to deviations in these processes. Several decades of research have contributed to our understanding of the central nervous system in health and disease, and we discuss that understanding the key processes involved in neuronal dysfunction and synaptic activity may be translated to the carotid body, offering new insights and avenues for therapeutic innovation.

Indexed as

GABAglutamatelong term potentiationsynaptic plasticitytype I cellstype II cells

Identifiers

PMID36046221
PMCPMC9420943
OpenAlexW4291377912

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.