Evidence map›Paper›PMID 30609840›Full record

ArticleInternational journal of molecular sciences2019

Overexpression of P2X3 and P2X7 Receptors and TRPV1 Channels in Adrenomedullary Chromaffin Cells in a Rat Model of Neuropathic Pain.

Marina Arribas-Blázquez, Luis Alcides Olivos-Oré, María Victoria Barahona, Mercedes Sánchez de la Muela, Virginia Solar, Esperanza Jiménez, Javier Gualix, J Michael McIntosh, Antonio Ferrer-Montiel, María Teresa Miras-Portugal and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

18 citing papers in PubMed, 43 citations in OpenAlex.

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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

11 authors at 3 institutions in 2 countries.

Marina Arribas-BlázquezDepartment of Pharmacology and Toxicology, Veterinary Faculty, Universidad Complutense de Madrid, 28040 Madrid, Spain. marina.arribas@vet.ucm.es.
Luis Alcides Olivos-OréDepartment of Pharmacology and Toxicology, Veterinary Faculty, Universidad Complutense de Madrid, 28040 Madrid, Spain. olivos@ucm.es.
María Victoria BarahonaDepartment of Pharmacology and Toxicology, Veterinary Faculty, Universidad Complutense de Madrid, 28040 Madrid, Spain. vbg@ucm.es.
Mercedes Sánchez de la MuelaDepartment of Animal Medicine and Surgery, Veterinary Faculty, Universidad Complutense de Madrid, 28040 Madrid, Spain. sdlmuela@vet.ucm.es.
Virginia SolarDepartment of Pharmacology and Toxicology, Veterinary Faculty, Universidad Complutense de Madrid, 28040 Madrid, Spain. virvir93@gmail.com.
Esperanza JiménezDepartment of Pharmacology and Toxicology, Veterinary Faculty, Universidad Complutense de Madrid, 28040 Madrid, Spain. esperanzajim@gmail.com.
Javier GualixInstituto Universitario de Investigación en Neuroquímica, Universidad Complutense de Madrid, 28040 Madrid, Spain. jgualix@ucm.es.
J Michael McIntoshGeorge E. Wahlen Veterans Affairs Medical Center, Salt Lake City, UT 84148, USA. mcintosh.mike@gmail.com.
Antonio Ferrer-MontielInstituto de Biología Molecular y Celular (IBMC), Universitas Miguel Hernández, 03202 Elche, Spain. aferrer@umh.es.
María Teresa Miras-PortugalInstituto Universitario de Investigación en Neuroquímica, Universidad Complutense de Madrid, 28040 Madrid, Spain. mtmiras@vet.ucm.es.
Antonio R ArtalejoDepartment of Pharmacology and Toxicology, Veterinary Faculty, Universidad Complutense de Madrid, 28040 Madrid, Spain. antonio.artalejo@vet.ucm.es.ORCID 0000-0001-9720-9190
Universidad Complutense de Madrid · ESUniversitat de Miguel Hernández d'Elx · ESUniversity of Utah · US

Funding

Venoms, Biological Resources, Molecular BiologyP01GM048677 · NIGMS · UNIVERSITY OF UTAH · PI OLIVERA, BALDOMERO M · 1993 to 2018
$32.2M
Novel nAChR-Targeted PeptidesR01GM103801 · NIGMS · UNIVERSITY OF UTAH · PI MCINTOSH, J MICHAEL · 2012 to 2019
$2.4M
NIGMS NIH HHS P01 GM048677NIGMS NIH HHS R01 GM103801
6 · The paper itself

Abstract

We have tested the hypothesis that neuropathic pain acting as a stressor drives functional plasticity in the sympathoadrenal system. The relation between neuropathic pain and adrenal medulla function was studied with behavioral, immunohistochemical and electrophysiological techniques in rats subjected to chronic constriction injury of the sciatic nerve. In slices of the adrenal gland from neuropathic animals, we have evidenced increased cholinergic innervation and spontaneous synaptic activity at the splanchnic nerve⁻chromaffin cell junction. Likewise, adrenomedullary chromaffin cells displayed enlarged acetylcholine-evoked currents with greater sensitivity to α-conotoxin RgIA, a selective blocker of α9 subunit-containing nicotinic acetylcholine receptors, as well as increased exocytosis triggered by voltage-activated Ca

Indexed as

AcetylcholineAdenosine TriphosphateAdrenal MedullaAnimalsCapsaicinCatecholaminesChromaffin CellsDisease Models, AnimalEvoked PotentialsExocytosisGanglia, SpinalMaleMembrane PotentialsNeuralgiaNeuronsRatsAcetylcholineAdenosine Triphosphatealpha,beta-methyleneadenosine 5'-triphosphateCapsaicinCatecholaminesReceptors, Purinergic P2X3Receptors, Purinergic P2X7Trpv1 protein, ratTRPV Cation Channelsadrenal medullachromaffin cellsneuropathic painP2X3 receptorsP2X7 receptorsstressTRPV1 channelsα9 nicotinic acetylcholine receptors

Identifiers

PMID30609840
PMCPMC6337219
OpenAlexW2908047436

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.