Evidence map›Paper›PMID 25745388›Full record

ArticleFrontiers in systems neuroscience2015

Identifying the integrated neural networks involved in capsaicin-induced pain using fMRI in awake TRPV1 knockout and wild-type rats.

Jason R Yee, William Kenkel, John C Caccaviello, Kevin Gamber, Phil Simmons, Mark Nedelman, Praveen Kulkarni, Craig F Ferris

Open access · goldAbstract read
In one paragraph

Article in Frontiers in systems neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Where do we stand on fMRI in awake mice?Cerebral cortex (New York, N.Y. : 1991) · 2024
    Pooled it
  2. Review
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  16. Brain mechanisms mediating effects of stress on reward sensitivity.Current opinion in behavioral sciences · 2018
    Article
  17. Article
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  19. Hypernatremia-induced vasopressin secretion is not altered in TRPV1-/- rats.American journal of physiology. Regulatory, integrative and comparative physiology · 2016
    Article
  20. Review
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

8 authors at 1 institution in 1 country.

Jason R YeeCenter for Translational NeuroImaging, Department of Psychology, Northeastern University Boston, MA, USA.
William KenkelCenter for Translational NeuroImaging, Department of Psychology, Northeastern University Boston, MA, USA.
John C CaccavielloCenter for Translational NeuroImaging, Department of Psychology, Northeastern University Boston, MA, USA.
Kevin GamberSAGE Labs St Louis, MO, USA.
Phil SimmonsSAGE Labs St Louis, MO, USA.
Mark NedelmanEkam Imaging Boston, MA, USA.
Praveen KulkarniCenter for Translational NeuroImaging, Department of Psychology, Northeastern University Boston, MA, USA.
Craig F FerrisCenter for Translational NeuroImaging, Department of Psychology, Northeastern University Boston, MA, USA.
Northeastern University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the present study, we used functional MRI in awake rats to investigate the pain response that accompanies intradermal injection of capsaicin into the hindpaw. To this end, we used BOLD imaging together with a 3D segmented, annotated rat atlas and computational analysis to identify the integrated neural circuits involved in capsaicin-induced pain. The specificity of the pain response to capsaicin was tested in a transgenic model that contains a biallelic deletion of the gene encoding for the transient receptor potential cation channel subfamily V member 1 (TRPV1). Capsaicin is an exogenous ligand for the TRPV1 receptor, and in wild-type rats, activated the putative pain neural circuit. In addition, capsaicin-treated wild-type rats exhibited activation in brain regions comprising the Papez circuit and habenular system, systems that play important roles in the integration of emotional information, and learning and memory of aversive information, respectively. As expected, capsaicin administration to TRPV1-KO rats failed to elicit the robust BOLD activation pattern observed in wild-type controls. However, the intradermal injection of formalin elicited a significant activation of the putative pain pathway as represented by such areas as the anterior cingulate, somatosensory cortex, parabrachial nucleus, and periaqueductal gray. Notably, comparison of neural responses to capsaicin in wild-type vs. knock-out rats uncovered evidence that capsaicin may function in an antinociceptive capacity independent of TRPV1 signaling. Our data suggest that neuroimaging of pain in awake, conscious animals has the potential to inform the neurobiological basis of full and integrated perceptions of pain.

Indexed as

capsaicinfMRI BOLDfMRI methodshabenulapain networksPapez circuitTRPV1

Identifiers

PMID25745388
PMCPMC4333803
OpenAlexW1970683451

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.