Evidence map›Paper›PMID 26797506›Full record

ArticlePain2016

Cell cycle inhibition limits development and maintenance of neuropathic pain following spinal cord injury.

Junfang Wu, Zaorui Zhao, Xiya Zhu, Cynthia L Renn, Susan G Dorsey, Alan I Faden

Open access · greenAbstract read
In one paragraph

Article in Pain, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
5.5field-weighted citation impact, top 4% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 67 citations in OpenAlex.

  1. Pooled it
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  18. Application of Bioinformatics Methods to Identify Key Genes and Functions in Chronic Pelvic Pain.Evidence-based complementary and alternative medicine : eCAM · 2021
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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

6 authors at 1 institution in 1 country.

Junfang WuDepartment of Anesthesiology and Center for Shock, Trauma and Anesthesiology Research (STAR), University of Maryland School of Medicine, Baltimore, MD, USA Department of Anatomy and Neurobiology, University of Maryland School of Medicine, Baltimore, MD, USA Department of Pain and Translational Symptom Science, University of Maryland School of Nursing, Baltimore, MD, USA.
Zaorui Zhao
Xiya Zhu
Cynthia L Renn
Susan G Dorsey
Alan I Faden
University of Maryland, Baltimore · US

Funding

Spinal Mechanisms Underlying SCI-Induced Pain: Implications for Targeted TherapyR01NR013601 · NINR · UNIVERSITY OF MARYLAND BALTIMORE · PI DORSEY, SUSAN G, FADEN, ALAN IRA · 2012 to 2021
$6.0M
Translational Phenotyping CoreP30NR014129 · NINR · UNIVERSITY OF MARYLAND BALTIMORE · PI DORSEY, SUSAN G · 2012 to 2016
$2.3M
Cell Cycle Pathway Inhibition Decreases Peripheral Neuropathic PainR21NR014053 · NINR · UNIVERSITY OF MARYLAND BALTIMORE · PI RENN, CYNTHIA L, WU, JUNFANG · 2013 to 2014
$420k
NINR NIH HHS P30 NR014129NINR NIH HHS R01 NR013601NINR NIH HHS R21 NR014053
6 · The paper itself

Abstract

Chronic pain after spinal cord injury (SCI) may present as hyperalgesia, allodynia, and/or spontaneous pain and is often resistant to conventional pain medications. Identifying more effective interventions to manage SCI pain requires improved understanding of the pathophysiological mechanisms involved. Cell cycle activation (CCA) has been implicated as a key pathophysiological event following SCI. We have shown that early central or systemic administration of a cell cycle inhibitor reduces CCA, prevents glial changes, and limits SCI-induced hyperesthesia. Here, we compared the effects of early vs late treatment with the pan-cyclin-dependent kinase inhibitor flavopiridol on allodynia as well as spontaneous pain. Adult C57BL/6 male mice subjected to moderate SCI were treated with intraperitoneal injections of flavopiridol (1 mg/kg), daily for 7 days beginning either 3 hours or 5 weeks after injury. Mechanical/thermal allodynia was evaluated, as well as spontaneous pain using the mouse grimace scale (MGS). We show that sensitivity to mechanical and thermal stimulation, and locomotor dysfunction were significantly reduced by early flavopiridol treatment compared with vehicle-treated controls. Spinal cord injury caused robust and extended increases of MGS up to 3 weeks after trauma. Early administration of flavopiridol significantly shortened duration of MGS changes. Late flavopiridol intervention significantly limited hyperesthesia at 7 days after treatment, associated with reduced glial changes, but without effect on locomotion. Thus, our data suggest that cell cycle modulation may provide an effective therapeutic strategy to reduce hyperesthesia after SCI, with a prolonged therapeutic window.

Indexed as

Cell CycleFlavonoidsNeuralgiaPiperidinesProtein Kinase InhibitorsSpinal Cord InjuriesAnimalsCalcium-Binding ProteinsCell Cycle ProteinsCell MovementDisease Models, AnimalFacial ExpressionGanglia, SpinalGene Expression RegulationHyperalgesiaLocomotionAif1 protein, mousealvocidibCalcium-Binding ProteinsCell Cycle ProteinsFlavonoidsMicrofilament ProteinsNerve Tissue ProteinsPiperidinesProtein Kinase Inhibitors

Identifiers

PMID26797506
PMCPMC4881432
OpenAlexW2468124354

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.