Evidence map›Paper›PMID 32429423›Full record

ArticleBioengineering (Basel, Switzerland)2020

Conserved Expression of Nav1.7 and Nav1.8 Contribute to the Spontaneous and Thermally Evoked Excitability in IL-6 and NGF-Sensitized Adult Dorsal Root Ganglion Neurons In Vitro.

Rahul R Atmaramani, Bryan J Black, June Bryan de la Peña, Zachary T Campbell, Joseph J Pancrazio

Open access · goldAbstract read
In one paragraph

Article in Bioengineering (Basel, Switzerland), 2020. 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
1.1field-weighted citation impact, top 24% 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, 19 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

5 authors at 1 institution in 1 country.

Rahul R AtmaramaniDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX 75080, USA.ORCID 0000-0002-9325-547X
Bryan J BlackDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX 75080, USA.
June Bryan de la PeñaCenter for Advanced Pain Studies, University of Texas at Dallas, Richardson, TX 75080, USA.
Zachary T CampbellCenter for Advanced Pain Studies, University of Texas at Dallas, Richardson, TX 75080, USA.ORCID 0000-0002-3768-6996
Joseph J PancrazioDepartment of Bioengineering, University of Texas at Dallas, Richardson, TX 75080, USA.
The University of Texas at Dallas · US

Funding

3’ End Regulation in Nociceptor PlasticityR01NS100788 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI CAMPBELL, ZACHARY · 2017 to 2021
$2.0M
hiPSC-based DRG Tissue Mimics on Multi-well Microelectrode Arrays as a Tissue Chip Model of Acute and Chronic NociceptionUG3TR003149 · NCATS · UNIVERSITY OF TEXAS DALLAS · PI BLACK, BRYAN JAMES · 2019 to 2020
$981k
hiPSC-based DRG Tissue Mimics on Multi-well Microelectrode Arrays as a Tissue Chip Model of Acute and Chronic NociceptionUH3TR003149 · NCATS · UNIVERSITY OF MASSACHUSETTS LOWELL · PI BLACK, BRYAN JAMES · 2021 to 2021
$845k
Center for Advanced Pain Studies N/ANCATS NIH HHS UG3 TR003149NCATS NIH HHS UH3 TR003149NIH HHS R01NS100788
6 · The paper itself

Abstract

Sensory neurons respond to noxious stimuli by relaying information from the periphery to the central nervous system via action potentials driven by voltage-gated sodium channels, specifically Nav1.7 and Nav1.8. These channels play a key role in the manifestation of inflammatory pain. The ability to screen compounds that modulate voltage-gated sodium channels using cell-based assays assumes that key channels present in vivo is maintained in vitro. Prior electrophysiological work in vitro utilized acutely dissociated tissues, however, maintaining this preparation for long periods is difficult. A potential alternative involves multi-electrode arrays which permit long-term measurements of neural spike activity and are well suited for assessing persistent sensitization consistent with chronic pain. Here, we demonstrate that the addition of two inflammatory mediators associated with chronic inflammatory pain, nerve growth factor (NGF) and interleukin-6 (IL-6), to adult DRG neurons increases their firing rates on multi-electrode arrays in vitro. Nav1.7 and Nav1.8 proteins are readily detected in cultured neurons and contribute to evoked activity. The blockade of both Nav1.7 and Nav1.8, has a profound impact on thermally evoked firing after treatment with IL-6 and NGF. This work underscores the utility of multi-electrode arrays for pharmacological studies of sensory neurons and may facilitate the discovery and mechanistic analyses of anti-nociceptive compounds.

Indexed as

dorsal root ganglionIL-6inflammationmicroelectrode arraysNav1.7Nav1.8NGFnociceptor

Identifiers

PMID32429423
PMCPMC7356605
OpenAlexW3024086846

What OpenQuestion 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 OpenQuestion graph.