Evidence map›Paper›PMID 24733934›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Defining modulatory inputs into CNS neuronal subclasses by functional pharmacological profiling.

Shrinivasan Raghuraman, Alfredo J Garcia, Tatiana M Anderson, Vernon D Twede, Kigen J Curtice, Kevin Chase, Jan-Marino Ramirez, Baldomero M Olivera, Russell W Teichert

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. An integrative approach to the facile functional classification of dorsal root ganglion neuronal subclasses.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Constellation pharmacology: a new paradigm for drug discovery.Annual review of pharmacology and toxicology · 2015
    Review
  11. 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

9 authors at 3 institutions in 1 country.

Shrinivasan RaghuramanDepartment of Biology, University of Utah, Salt Lake City, UT 84112.
Alfredo J Garcia
Tatiana M Anderson
Vernon D Twede
Kigen J Curtice
Kevin Chase
Jan-Marino Ramirez
Baldomero M Olivera
Russell W Teichert
University of Utah · USNeurological Surgery · USSeattle Children's Hospital · US

Funding

Venoms, Biological Resources, Molecular BiologyP01GM048677 · NIGMS · UNIVERSITY OF UTAH · PI BANDYOPADHYAY, PRADIP K · 1993 to 2018
$32.2M
Integrative Consequences of HypoxiaP01HL090554 · NHLBI · UNIVERSITY OF CHICAGO · PI PRABHAKAR, NANDURI R · 2008 to 2017
$21.4M
NHLBI NIH HHS P01 HL090554NIGMS NIH HHS GM48677NIGMS NIH HHS P01 GM048677
6 · The paper itself

Abstract

Previously we defined neuronal subclasses within the mouse peripheral nervous system using an experimental strategy called "constellation pharmacology." Here we demonstrate the broad applicability of constellation pharmacology by extending it to the CNS and specifically to the ventral respiratory column (VRC) of mouse brainstem, a region containing the neuronal network controlling respiratory rhythm. Analysis of dissociated cells from this locus revealed three major cell classes, each encompassing multiple subclasses. We broadly analyzed the combinations (constellations) of receptors and ion channels expressed within VRC cell classes and subclasses. These were strikingly different from the constellations of receptors and ion channels found in subclasses of peripheral neurons from mouse dorsal root ganglia. Within the VRC cell population, a subset of dissociated neurons responded to substance P, putatively corresponding to inspiratory pre-Bötzinger complex (preBötC) neurons. Using constellation pharmacology, we found that these substance P-responsive neurons also responded to histamine, and about half responded to bradykinin. Electrophysiological studies conducted in brainstem slices confirmed that preBötC neurons responsive to substance P exhibited similar responsiveness to bradykinin and histamine. The results demonstrate the predictive utility of constellation pharmacology for defining modulatory inputs into specific neuronal subclasses within central neuronal networks.

Indexed as

AnimalsBradykininBrain StemCalciumCells, CulturedCentral Nervous SystemCluster AnalysisFemaleGanglia, SpinalHistamineImaging, Three-DimensionalMaleMiceMice, Inbred C57BLNerve NetNeuronsBradykininCalciumHistamineReceptors, CholinergicReceptors, GlutamateSubstance Pacetylcholinecalcium imagingconotoxinglutamateNK1 receptor

Identifiers

PMID24733934
PMCPMC4035978
OpenAlexW1996069021

What OpenQuestion holds

Textmetadata
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.