Evidence map›Paper›PMID 22535545›Full record

ArticleJournal of neuroscience research2012

Postinjury treatment with rolipram increases hemorrhage after traumatic brain injury.

C M Atkins, Y Kang, C Furones, J S Truettner, O F Alonso, W D Dietrich

Abstract read
In one paragraph

Article in Journal of neuroscience research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Chronic Cognitive Dysfunction after Traumatic Brain Injury Is Improved with a Phosphodiesterase 4B Inhibitor.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Article
  6. Article
  7. Review
  8. Review
  9. Effects of PDE4 pathway inhibition in rat experimental stroke.Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques · 2014
    Article
  10. Article
  11. Phosphodiesterase inhibition rescues chronic cognitive deficits induced by traumatic brain injury.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  12. Article
  13. 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

6 authors at 2 institutions in 1 country.

C M AtkinsThe Miami Project to Cure Paralysis, Department of Neurological Surgery, University of Miami Miller School of Medicine, Miami, Florida, USA. catkins@med.miami.edu
Y Kang
C Furones
J S Truettner
O F Alonso
W D Dietrich
Neurological Surgery · USUniversity of Miami · US

Funding

TRAUMATIC BRAIN INJURY INDUCED SEIZURE & SYNAPTIC PLASTICITYP50NS030291 · NINDS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI GREEN, EDWARD J · 1991 to 2013
$14.8M
Cyclic Nucleotide Regulation in Traumatic Brain Injury and Alzheimer's DiseaseR01NS056072 · NINDS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI ATKINS, COLEEN M., DIETRICH, W DALTON · 2007 to 2018
$4.1M
Rehabilitation Strategies for Memory Dysfunction After Traumatic Brain InjuryR01NS069721 · NINDS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI ATKINS, COLEEN M. · 2010 to 2019
$3.7M
NINDS NIH HHS NS056072NINDS NIH HHS NS069721NINDS NIH HHS P50 NS030291NINDS NIH HHS R01 NS056072NINDS NIH HHS R01 NS069721
6 · The paper itself

Abstract

The pathology caused by traumatic brain injury (TBI) is exacerbated by the inflammatory response of the injured brain. Two proinflammatory cytokines that contribute to inflammation after TBI are tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β). From previous studies using the parasagittal fluid-percussion brain injury model, we reported that the anti-inflammatory drug rolipram, a phosphodiesterase 4 inhibitor, reduced TNF-α and IL-1β levels and improved histopathological outcome when administered 30 min prior to injury. We now report that treatment with (±)-rolipram given 30 min after injury significantly reduced TNF-α levels in the cortex and hippocampus. However, postinjury administration of (±)-rolipram significantly increased cortical contusion volume and increased atrophy of the cortex compared with vehicle-treated animals at 10 days postinjury. Thus, despite the reduction in proinflammatory cytokine levels, histopathological outcome was worsened with post-TBI (±)-rolipram treatment. Further histological analysis of (±)-rolipram-treated TBI animals revealed significant hemorrhage in the contused brain. Given the well-known role of (±)-rolipram of increasing vasodilation, it is likely that (±)-rolipram worsened outcome after fluid-percussion brain injury by causing increased bleeding.

Indexed as

AnimalsBrain InjuriesCerebral HemorrhageCerebrovascular CirculationDisease Models, AnimalEnzyme-Linked Immunosorbent AssayImmunohistochemistryMalePhosphodiesterase 4 InhibitorsRatsRats, Sprague-DawleyRolipramTumor Necrosis Factor-alphaPhosphodiesterase 4 InhibitorsRolipramTumor Necrosis Factor-alpha

Identifiers

PMID22535545
PMCPMC3418599
OpenAlexW2122701866

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.