Evidence map›Paper›PMID 36834743›Full record

ReviewInternational journal of molecular sciences2023

P188 Therapy in In Vitro Models of Traumatic Brain Injury.

Michael Zargari, Luise J Meyer, Matthias L Riess, Zhu Li, Matthew B Barajas

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Effects of poloxamer 188 on traumatic brain injury.Brain, behavior, & immunity - health · 2024
    Review
  4. Article
  5. Review
  6. Blood-Brain Barrier Breakdown in Neuroinflammation: Current In Vitro Models.International journal of molecular sciences · 2023
    Review
  7. 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

5 authors at 4 institutions in 2 countries.

Michael ZargariVanderbilt University School of Medicine, Nashville, TN 37232, USA.ORCID 0000-0001-5905-3156
Luise J MeyerAlbertinen Krankenhaus, 22457 Hamburg, Germany.
Matthias L RiessTVHS VA Medical Center, Anesthesiology, Nashville, TN 37212, USA.ORCID 0000-0001-8748-5757
Zhu LiDepartment of Anesthesiology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.ORCID 0000-0001-6228-8845
Matthew B BarajasTVHS VA Medical Center, Anesthesiology, Nashville, TN 37212, USA.ORCID 0000-0002-3313-3112
Vanderbilt University · USAlbertinen Diakoniewerk · DENashville VA Medical Center · USVanderbilt University Medical Center · US

Funding

TIPS: Training in Perioperative ScienceT32GM108554 · NIGMS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Eric J Delpire · 2014 to 2026
$3.7M
Novel Copolymer-based Cell Membrane Stabilizers to Attenuate Myocardial InfarctionI01BX003482 · VA · VETERANS HEALTH ADMINISTRATION · PI RIESS, MATTHIAS L. · 2018 to 2022
–
BLRD VA I01 BX003482NIGMS NIH HHS T32 GM108554NIH HHS 5T32 GM108554
6 · The paper itself

Abstract

Traumatic brain injury (TBI) is a significant cause of morbidity and mortality worldwide. Varied mechanisms of injury contribute to the heterogeneity of this patient population as demonstrated by the multiple published grading scales and diverse required criteria leading to diagnoses from mild to severe. TBI pathophysiology is classically separated into a primary injury that is characterized by local tissue destruction as a result of the initial blow, followed by a secondary phase of injury constituted by a score of incompletely understood cellular processes including reperfusion injury, disruption to the blood-brain barrier, excitotoxicity, and metabolic dysregulation. There are currently no effective pharmacological treatments in the wide-spread use for TBI, in large part due to challenges associated with the development of clinically representative in vitro and in vivo models. Poloxamer 188 (P188), a Food and Drug Administration-approved amphiphilic triblock copolymer embeds itself into the plasma membrane of damaged cells. P188 has been shown to have neuroprotective properties on various cell types. The objective of this review is to provide a summary of the current literature on in vitro models of TBI treated with P188.

Indexed as

Brain Injuries, TraumaticPoloxamerBlood-Brain BarrierCell MembraneHumansNeuronsPoloxamercell membrane stabilizerconcussioncopolymerneuroprotectionPoloxamer 188TBI

Identifiers

PMID36834743
PMCPMC9961452
OpenAlexW4319600697

What Socratic 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 Socratic graph.