Evidence map›Paper›PMID 25271163›Full record

ArticleThe Journal of biological chemistry2014

Chemical structure and morphology of dorsal root ganglion neurons from naive and inflamed mice.

Marie E Barabas, Eric C Mattson, Ebrahim Aboualizadeh, Carol J Hirschmugl, Cheryl L Stucky

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.1field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 30 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.

Marie E BarabasFrom the Department of Cell Biology, Neurobiology and Anatomy, Medical College of Wisconsin, Milwaukee, Wisconsin 53226-0509 and.
Eric C Mattsonthe Department of Physics, University of Wisconsin-Milwaukee, Milwaukee, Wisconsin 53211.
Ebrahim Aboualizadehthe Department of Physics, University of Wisconsin-Milwaukee, Milwaukee, Wisconsin 53211.
Carol J Hirschmuglthe Department of Physics, University of Wisconsin-Milwaukee, Milwaukee, Wisconsin 53211.
Cheryl L StuckyFrom the Department of Cell Biology, Neurobiology and Anatomy, Medical College of Wisconsin, Milwaukee, Wisconsin 53226-0509 and cstucky@mcw.edu.
Medical College of Wisconsin · US

Funding

Nociceptive Mechanisms Underlying Sickle Cell PainR01NS070711 · NINDS · MEDICAL COLLEGE OF WISCONSIN · PI Bonnie N Dittel, Cheryl Louise Stucky · 2009 to 2026
$8.7M
FUNCTIONAL ANALYSIS OF DISTINCT NOCICEPTOR POPULATIONSR01NS040538 · NINDS · MEDICAL COLLEGE OF WISCONSIN · PI STUCKY, CHERYL LOUISE · 2000 to 2019
$6.2M
NINDS NIH HHS NS040538NINDS NIH HHS NS070711NINDS NIH HHS R01 NS040538NINDS NIH HHS R01 NS070711
6 · The paper itself

Abstract

Fourier transform infrared spectromicroscopy provides label-free imaging to detect the spatial distribution of the characteristic functional groups in proteins, lipids, phosphates, and carbohydrates simultaneously in individual DRG neurons. We have identified ring-shaped distributions of lipid and/or carbohydrate enrichment in subpopulations of neurons which has never before been reported. These distributions are ring-shaped within the cytoplasm and are likely representative of the endoplasmic reticulum. The prevalence of chemical ring subtypes differs between large- and small-diameter neurons. Peripheral inflammation increased the relative lipid content specifically in small-diameter neurons, many of which are nociceptive. Because many small-diameter neurons express an ion channel involved in inflammatory pain, transient receptor potential ankyrin 1 (TRPA1), we asked whether this increase in lipid content occurs in TRPA1-deficient (knock-out) neurons. No statistically significant change in lipid content occurred in TRPA1-deficient neurons, indicating that the inflammation-mediated increase in lipid content is largely dependent on TRPA1. Because TRPA1 is known to mediate mechanical and cold sensitization that accompanies peripheral inflammation, our findings may have important implications for a potential role of lipids in inflammatory pain.

Indexed as

AnimalsCarbohydratesCell SizeFreund's AdjuvantGanglia, SpinalGene ExpressionHindlimbInflammationInjections, SubcutaneousLipidsMaleMiceMice, Inbred C57BLMice, TransgenicPainPrimary Cell CultureCarbohydratesFreund's AdjuvantLipidsTransient Receptor Potential ChannelsTRPA1 Cation ChannelTrpa1 protein, mouseComplete Freund's AdjuvantDorsal Root GangliaInflammationInfrared Spectroscopy (IR Spectroscopy)LipidMechanotransductionNociceptorPainSensory NeuronTransient Receptor Potential Ankyrin 1Transient Receptor Potential Channels (TRP Channels)

Identifiers

PMID25271163
PMCPMC4256355
OpenAlexW1986385425

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.