Evidence map›Paper›PMID 23532086›Full record

ArticleJournal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism2013

TIMP-1 attenuates blood-brain barrier permeability in mice with acute liver failure.

Feng Chen, Evette S Radisky, Pritam Das, Jyotica Batra, Toshiyuki Hata, Tomohide Hori, Ann-Marie T Baine, Lindsay Gardner, Mei Y Yue, Guojun Bu and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The TIMP protein family: diverse roles in pathophysiology.American journal of physiology. Cell physiology · 2024
    Review
  5. Review
  6. Article
  7. Review
  8. The neurogliovascular unit in hepatic encephalopathy.JHEP reports : innovation in hepatology · 2021
    Review
  9. Article
  10. Article
  11. EPStem cells translational medicine · 2019
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Annexin A1 restores AβAging cell · 2017
    Article
  19. Article
  20. 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

13 authors at 4 institutions in 1 country.

Feng ChenDepartment of Neuroscience, Mayo Clinic, Jacksonville, Florida, USA.
Evette S Radisky
Pritam Das
Jyotica Batra
Toshiyuki Hata
Tomohide Hori
Ann-Marie T Baine
Lindsay Gardner
Mei Y Yue
Guojun Bu
Gregory del Zoppo
Tushar C Patel
Justin H Nguyen
Mayo Clinic in Florida · USJacksonville College · USMayo Clinic · USWinnMed · US

Funding

Neurovascular Adhesion Receptors and Barrier IntegrityR01NS053716 · NINDS · UNIVERSITY OF WASHINGTON · PI DEL ZOPPO, GREGORY J · 2006 to 2016
$3.5M
Matrix Metalloproteinases and Neurons in Focal IschemiaR37NS038710 · NINDS · UNIVERSITY OF WASHINGTON · PI DEL ZOPPO, GREGORY J · 2004 to 2010
$3.2M
MMP-9 in Blood-Brain Barrier Failure in Fulminant Hepatic FailureR01NS051646 · NINDS · MAYO CLINIC JACKSONVILLE · PI NGUYEN, JUSTIN H · 2007 to 2009
$821k
NINDS NIH HHS R01 NS051646NINDS NIH HHS R01NS051646-01A2NINDS NIH HHS R01 NS053716NINDS NIH HHS R37 NS038710
6 · The paper itself

Abstract

Blood-brain barrier (BBB) dysfunction in acute liver failure (ALF) results in increased BBB permeability that often precludes the patients from obtaining a life-saving liver transplantation. It remains controversial whether matrix metalloproteinase-9 (MMP-9) from the injured liver contributes to the deregulation of BBB function in ALF. We selectively upregulated a physiologic inhibitor of MMP-9 (TIMP-1) with a single intracerebroventricular injection of TIMP-1 cDNA plasmids at 48 and 72 hours, or with pegylated-TIMP-1 protein. Acute liver failure was induced with tumor necrosis factor-α and D-(+)-galactosamine in mice. Permeability of BBB was assessed with sodium fluorescein (NaF) extravasation. We found a significant increase in TIMP-1 within the central nervous system (CNS) after the administration of TIMP-1 cDNA plasmids and that increased TIMP-1 within the CNS resulted in an attenuation of BBB permeability, a reduction in activation of epidermal growth factor receptor and p38 mitogen-activated protein kinase signals, and a restoration of the tight junction protein occludin in mice with experimental ALF. Pegylated TIMP-1 provided similar protection against BBB permeability in mice with ALF. Our results provided a proof of principle that MMP-9 contributes to the BBB dysfunction in ALF and suggests a potential therapeutic role of TIMP-1 in ALF.

Indexed as

AnimalsBlood-Brain BarrierBlotting, WesternCapillary PermeabilityDNA, ComplementaryImmunohistochemistryInjections, IntraventricularLiver Failure, AcuteMaleMatrix Metalloproteinase 9MiceMice, Inbred C57BLPlasmidsTissue Inhibitor of Metalloproteinase-1Up-RegulationDNA, ComplementaryMatrix Metalloproteinase 9Timp1 protein, mouseTissue Inhibitor of Metalloproteinase-1

Identifiers

PMID23532086
PMCPMC3705430
OpenAlexW1994029628

What OpenQuestion holds

Textmetadata
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.