Evidence map›Paper›PMID 28391012›Full record

ArticleNeuroscience2017

Mapping of pain circuitry in early post-natal development using manganese-enhanced MRI in rats.

M M Sperry, B M Kandel, S Wehrli, K N Bass, S R Das, P S Dhillon, J C Gee, G A Barr

Open access · greenAbstract read
In one paragraph

Article in Neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.5field-weighted citation impact, top 6% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Quality Assurance Strategies for Brain State Characterization by MEMRI.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Review
  5. Fetal programming of human energy homeostasis brain networks: Issues and considerations.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2022
    Review
  6. Article
  7. The development of pain circuits and unique effects of neonatal injury.Journal of neural transmission (Vienna, Austria : 1996) · 2020
    Review
  8. Article
  9. Review
  10. Article
  11. Article
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 2 institutions in 1 country.

M M SperryDepartment of Bioengineering, University of Pennsylvania, United States.
B M KandelPenn Image Computing and Science Laboratory, Department of Radiology, University of Pennsylvania, United States.
S WehrliNMR Core, Children's Hospital of Philadelphia, United States.
K N BassAnesthesiology and Critical Care Medicine, Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania, United States.
S R DasPenn Image Computing and Science Laboratory, Department of Radiology, University of Pennsylvania, United States.
P S DhillonPenn Image Computing and Science Laboratory, Department of Radiology, University of Pennsylvania, United States.
J C GeePenn Image Computing and Science Laboratory, Department of Radiology, University of Pennsylvania, United States.
G A BarrAnesthesiology and Critical Care Medicine, Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania, United States. Electronic address: barrg@email.chop.edu.
University of Pennsylvania · USChildren's Hospital of Philadelphia · US

Funding

Training Program in Musculoskeletal ResearchT32AR007132 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI Robert L Mauck, LOUIS J SOSLOWSKY · 1986 to 2026
$4.9M
Training Program in Biomedical Imaging and Information SciencesT32EB009384 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI GEE, JAMES C, IVES, ZACHARY · 2009 to 2023
$4.0M
NIAMS NIH HHS T32 AR007132NIBIB NIH HHS T32 EB009384
6 · The paper itself

Abstract

Premature or ill full-term infants are subject to a number of noxious procedures as part of their necessary medical care. Although we know that human infants show neural changes in response to such procedures, we know little of the sensory or affective brain circuitry activated by pain. In rodent models, the focus has been on spinal cord and, more recently, midbrain and medulla. The present study assesses activation of brain circuits using manganese-enhanced magnetic resonance imaging (MEMRI). Uptake of manganese, a paramagnetic contrast agent that is transported across active synapses and along axons, was measured in response to a hindpaw injection of dilute formalin in 12-day-old rat pups, the age at which rats begin to show aversion learning and which is roughly the equivalent of full-term human infants. Formalin induced the oft-reported biphasic response at this age and induced a conditioned aversion to cues associated with its injection, thus demonstrating the aversiveness of the stimulation. Morphometric analyses, structural equation modeling and co-expression analysis showed that limbic and sensory paths were activated, the most prominent of which were the prefrontal and anterior cingulate cortices, nucleus accumbens, amygdala, hypothalamus, several brainstem structures, and the cerebellum. Therefore, both sensory and affective circuits, which are activated by pain in the adult, can also be activated by noxious stimulation in 12-day-old rat pups.

Indexed as

Brain MappingMagnetic Resonance ImagingAge FactorsAnimalsAnimals, NewbornBrainChloridesDisease Models, AnimalFemaleFormaldehydeImage Processing, Computer-AssistedMaleManganese CompoundsPainPain MeasurementRatsChloridesFormaldehydemanganese chlorideManganese CompoundsbraincircuitrydevelopmentMRInociception

Identifiers

PMID28391012
PMCPMC7276061
OpenAlexW2604955506

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.