Evidence map›Paper›PMID 19171165›Full record

ReviewBrain research reviews2009

Nucleotide signaling and cutaneous mechanisms of pain transduction.

G Dussor, H R Koerber, A L Oaklander, F L Rice, D C Molliver

Abstract readReview
In one paragraph

Review in Brain research reviews, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

44 citing papers in PubMed, 77 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 4 institutions in 1 country.

G DussorDepartment of Pharmacology, The University of Arizona College of Medicine, Tucson, AZ 85724, USA.
H R Koerber
A L Oaklander
F L Rice
D C Molliver
University of Pittsburgh · USAlbany Medical Center Hospital · USMassachusetts General Hospital · USUniversity of Arizona · US

Funding

Neurite density in skin as a marker for neuropathic painR01NS042866 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI OAKLANDER, ANNE LOUISE · 2002 to 2005
$1.6M
Primary and Secondary Nociceptors in Persistent PainR01NS052848 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KOERBER, H RICHARD · 2006 to 2010
$1.6M
Pro- and Anti-Nociceptive Actions of P2y Nucleotide Receptors in Sensory NeuronsR01NS056122 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MOLLIVER, DEREK C · 2007 to 2010
$1.3M
Pathophysiology and diagnosis of neurological pain syndromesK24NS059892 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI OAKLANDER, ANNE LOUISE · 2008 to 2012
$949k
NINDS NIH HHS K24 NS059892NINDS NIH HHS K24NS059892NINDS NIH HHS NS056122NINDS NIH HHS R01 NS042866NINDS NIH HHS R01 NS052848NINDS NIH HHS R01 NS056122NINDS NIH HHS R01NS42866
6 · The paper itself

Abstract

Sensory neurons that innervate the skin provide critical information about physical contact between the organism and the environment, including information about potentially-damaging stimuli that give rise to the sensation of pain. These afferents also contribute to the maintenance of tissue homeostasis, inflammation and wound healing, while sensitization of sensory afferents after injury results in painful hypersensitivity and protective behavior. In contrast to the traditional view of primary afferent terminals as the sole site of sensory transduction, recent reports have lead to the intriguing idea that cells of the skin play an active role in the transduction of sensory stimuli. The search for molecules that transduce different types of sensory stimuli (mechanical, heat, chemical) at the axon terminal has yielded a wide range of potential effectors, many of which are expressed by keratinocytes as well as neurons. Emerging evidence underscores the importance of nucleotide signaling through P2X ionotropic and P2Y metabotropic receptors in pain processing, and implicates nucleotide signaling as a critical form of communication between cells of the skin, immune cells and sensory neurons. It is of great interest to determine whether pathological changes in these mechanisms contribute to chronic pain in human disease states such as complex regional pain syndrome (CRPS). This review discusses recent advances in our understanding of communication mechanisms between cells of the skin and sensory axons in the transduction of sensory input leading to pain.

Indexed as

Skin Physiological PhenomenaAdenosine TriphosphateAnimalsHumansNociceptorsNucleotidesPainReceptors, G-Protein-CoupledReceptors, PurinergicSensory Receptor CellsSignal TransductionSkinAdenosine TriphosphateNucleotidesReceptors, G-Protein-CoupledReceptors, Purinergic

Identifiers

PMID19171165
PMCPMC3201739
OpenAlexW1985703062

What OpenQuestion holds

Textmetadata
LicenceTDM
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.