Evidence map›Paper›PMID 22171826›Full record

ArticleBritish journal of haematology2012

Mouse models for studying pain in sickle disease: effects of strain, age, and acuteness.

David M Cain, Derek Vang, Donald A Simone, Robert P Hebbel, Kalpna Gupta

Open access · bronzeAbstract read
In one paragraph

Article in British journal of haematology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

73 citing papers in PubMed, 93 citations in OpenAlex.

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  11. ΔThe Journal of pharmacology and experimental therapeutics · 2024
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13 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

David M CainVascular Biology Center and Division of Hematology-Oncology-Transplantation, Department of Medicine, University of Minnesota Medical School, Minneapolis, MN, USA.
Derek Vang
Donald A Simone
Robert P Hebbel
Kalpna Gupta
University of Minnesota Medical Center · USUniversity of Minnesota · US

Funding

VASCULAR PATHOBIOLOGY OF SICKLE CELL DISEASEP01HL055552 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI HEBBEL, ROBERT P · 1995 to 2011
$17.3M
CANNABINOID MODULATION OF HYPERALGESIAR01DA011471 · NIDA · UNIVERSITY OF MINNESOTA TWIN CITIES · PI SIMONE, DONALD · 2000 to 2014
$4.2M
Opioid Activity in Endothelium in Sickle Cell Disease R01HL068802 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI GUPTA, KALPNA · 2002 to 2012
$2.6M
Characteristics and mechanisms of pain in sickle cell diseaseR01HL103733 · NHLBI · UNIVERSITY OF MINNESOTA · PI GUPTA, KALPNA, SIMONE, DONALD · 2010 to 2014
$1.9M
NHLBI NIH HHS HL103773NHLBI NIH HHS HL55552NHLBI NIH HHS HL68802NHLBI NIH HHS HL68802-06S1NHLBI NIH HHS HL68802-7S1NHLBI NIH HHS P01 HL055552NHLBI NIH HHS R01 HL068802NHLBI NIH HHS R01 HL103733NIDA NIH HHS DA011471NIDA NIH HHS R01 DA011471
6 · The paper itself

Abstract

The clinical management of severe pain associated with sickle cell disease (SCD) remains challenging. Development of an optimal therapy would be facilitated by use of murine model(s) with varying degrees of sickling and pain tests that are most sensitive to vaso-occlusion. We found that young (≤3 months old) NY1DD and S+S(Antilles) mice (having modest and moderate sickle phenotype, respectively) exhibited evidence of deep tissue/musculoskeletal pain. Deep tissue pain and cold sensitivity in S+S(Antilles) mice increased significantly with both age and incitement of hypoxia/reoxygenation (H/R). C57/BL6 mice (genetic background strain of NY1DD and S+S(Antilles) ) were hypersensitive to mechanical and heat stimuli, even without the sickle transgene. H/R treatment of HbSS-BERK mice with severe sickle phenotype resulted in significantly decreased withdrawal thresholds and enhanced mechanical, thermal and deep tissue hyperalgesia. Deep hyperalgesia incited by H/R in HbSS-BERK was ameliorated by CP 55940, a cannabinoid receptor agonist. Thus, assessment of deep tissue pain appears to be the most sensitive measure for studying pain mechanisms across mouse models of SCD, and HbSS-BERK mice may be the best model for vaso-occlusive and chronic pain of SCD.

Indexed as

Disease Models, AnimalMiceAge FactorsAnalgesicsAnemia, Sickle CellAnimalsCannabinoid Receptor AntagonistsCyclohexanolsHumansHyperalgesiaHypoxiaMice, Inbred C57BLMice, TransgenicPainPain MeasurementTemperature3-(2-hydroxy-4-(1,1-dimethylheptyl)phenyl)-4-(3-hydroxypropyl)cyclohexanolAnalgesicsCannabinoid Receptor AntagonistsCyclohexanols

Identifiers

PMID22171826
PMCPMC3779783
OpenAlexW1509243631

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.