Evidence map›Paper›PMID 19295156›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2009

Diffusion-weighted magnetic resonance imaging reversal by gene knockdown of matrix metalloproteinase-9 activities in live animal brains.

Christina H Liu, Zerong You, Charng-Ming Liu, Young R Kim, Michael J Whalen, Bruce R Rosen, Philip K Liu

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

  1. Trial
  2. Article
  3. Imaging rhodopsin degeneration in vivo in a new model of ocular ischemia in living mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2016
    Article
  4. Article
  5. Article
  6. Article
  7. MRI reveals differential effects of amphetamine exposure on neuroglia in vivo.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2013
    Article
  8. Article
  9. Review
  10. Noninvasive detection of neural progenitor cells in living brains by MRI.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2012
    Article
  11. Article
  12. DNA-based MRI probes for specific detection of chronic exposure to amphetamine in living brains.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2009
    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

7 authors at 3 institutions in 1 country.

Christina H LiuLaboratory for Transcript Targeting, Imaging and Repair, A. A. Martinos Center for Biomedical Imaging, Department of Radiology, and Department of Pediatrics, Massachusetts General Hospital, Charlestown, Massachusetts 02129, USA.
Zerong You
Charng-Ming Liu
Young R Kim
Michael J Whalen
Bruce R Rosen
Philip K Liu
Athinoula A. Martinos Center for Biomedical Imaging · USMassachusetts General Hospital · USTarget (United States) · US

Funding

ULTRAHIGH FIELD TECHNOLOGY FOR FUNCTIONAL IMAGINGP41RR014075 · NCRR · MASSACHUSETTS GENERAL HOSPITAL · PI ROSEN, BRUCE R · 1999 to 2011
$16.4M
Perfusion Imaging with Magnetic ResonanceR01EB002066 · NIBIB · MASSACHUSETTS GENERAL HOSPITAL · PI ROSEN, BRUCE R · 2003 to 2009
$3.6M
RIPK1: A new target for traumatic brain injury?R01NS064545 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI WHALEN, MICHAEL J · 2009 to 2013
$2.1M
Initiation of Cell Death after Traumatic Brain InjuryR01NS047447 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI WHALEN, MICHAEL J · 2005 to 2009
$1.7M
In vivo Profiling of Glial and Neuronal Activities in Psychostimulant AbuseR01DA026108 · NIDA · MASSACHUSETTS GENERAL HOSPITAL · PI LIU, PHILIP K · 2009 to 2010
$1.2M
Gene Repair in signal Transduction after CNS InjuryR01NS045845 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI LIU, PHILIP K · 2003 to 2006
$1.0M
MR Assessment of Altered Cerebral Gene Expression after Amphetamine ExposureR21DA024235 · NIDA · MASSACHUSETTS GENERAL HOSPITAL · PI LIU, PHILIP K · 2007 to 2008
$476k
Neurovascular Mechanisns of Brain Function and DiseaseR21NS057556 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI LIU, PHILIP K · 2007 to 2008
$470k
NCRR NIH HHS P41 RR014075NCRR NIH HHS SP41RR14075NIBIB NIH HHS R01 EB002066NIBIB NIH HHS R01EB002066NIDA NIH HHS R01 DA026108NIDA NIH HHS R21 DA024235NIDA NIH HHS R21DA024235NINDS NIH HHS R01 NS045845NINDS NIH HHS R01NS045845NINDS NIH HHS R01 NS047447NINDS NIH HHS R01NS047447NINDS NIH HHS R01 NS064545NINDS NIH HHS R21 NS057556NINDS NIH HHS R21NS057556
6 · The paper itself

Abstract

The involvement of matrix metalloproteinase-9 (MMP-9) activities in the development of abnormal water diffusion in the brain after cardiac arrest is not fully understood. We used magnetic resonance imaging to determine the correlation between MMP-9 activity and the mechanism of abnormal water diffusion after global cerebral ischemia (GCI)-induced brain damage in C57black6 mice. We induced GCI in mice by occluding both carotid arteries for 60 min, then allowing reperfusion. We labeled a short DNA that targets mmp-9 mRNA activity [phosphorothioate-modified oligodeoxynucleotide (sODN)-mmp9] or a control probe without intracellular target (sODN-Ran) with iron-based MR contrast agent [superparamagnetic iron oxide nanoparticle (SPION)-mmp9 or SPION-Ran] or fluorescein isothiocyanate (FITC)-sODN-mmp9 or FITC-sODN-Ran; we then delivered these probes by intracerebroventricular infusion or intraperitoneal injection within 3 h of reperfusion. At low dose (120 pmol/kg) the SPION-mmp9 probe was retained at significant levels in the striatum and cortex of living brains 10 h after GCI. Probe retention was validated by similar elevation of mmp-9 mRNA and antigens in postmortem samples taken from regions that exhibited GCI-induced hyperintensity in diffusion-weighted imaging, and a significant reduction in apparent diffusion coefficient (rADC, p = 0.0006, n = 12). At a higher dose (120 nmol/kg), the FITC-sODN-mmp9 probe revealed significant knockdown of MMP-9 activity, per zymography, and a reversal of striatal rADC (p = 0.004, n = 6). These observations were not duplicated in the control group. We conclude that expression of mmp-9 mRNA is associated with abnormal ADC after GCI.

Indexed as

AnimalsBrainDiffusion Magnetic Resonance ImagingGene Knockdown TechniquesMaleMatrix Metalloproteinase 9MiceMice, Inbred C57BLMatrix Metalloproteinase 9

Identifiers

PMID19295156
PMCPMC2726707
OpenAlexW2061571295

What OpenQuestion holds

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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.