Evidence map›Paper›PMID 19844242›Full record

ArticleJournal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism2010

Cyclooxygenase-1 and -2 differentially modulate lipopolysaccharide-induced blood-brain barrier disruption through matrix metalloproteinase activity.

Saba Aid, Afonso C Silva, Eduardo Candelario-Jalil, Sang-Ho Choi, Gary A Rosenberg, Francesca Bosetti

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, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

39 citing papers in PubMed, 69 citations in OpenAlex.

  1. Review
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  12. Review
  13. Is cyclooxygenase-1 involved in neuroinflammation?Journal of neuroscience research · 2021
    Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. The Role of Intestinal Bacteria and Gut-Brain Axis in Hepatic Encephalopathy.Frontiers in cellular and infection microbiology · 2020
    Review
  19. BioMed research international · 2019
    Article
  20. Review
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 4 institutions in 1 country.

Saba AidBrain Physiology and Metabolism Section, National Institute on Aging, NIH, Bethesda, Maryland 20892, USA.
Afonso C Silva
Eduardo Candelario-Jalil
Sang-Ho Choi
Gary A Rosenberg
Francesca Bosetti
National Institute on Aging · USUniversity of New Mexico · USNational Institute of Neurological Disorders and Stroke · USNational Institutes of Health · US

Funding

Investigation of the Modulators of Cerebrovascular CouplingZIANS003012 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI SILVA, AFONSO · 2009 to 2019
$15.4M
Role of cyclooxygenases in neuroinflammationZ01AG000425 · NIA · NATIONAL INSTITUTE ON AGING · PI BOSETTI, FRANCESCA · 2007 to 2008
$830k
Role of cyclooxygenases in neuroinflammationZIAAG000425 · NIA · NATIONAL INSTITUTE ON AGING · PI BOSETTI, FRANCESCA · 2009 to 2010
$682k
Intramural NIH HHS Z01 AG000425NINDS NIH HHS 5R01NS04547
6 · The paper itself

Abstract

Cyclooxygenases (COX) -1 and -2 are key regulators of innate immune responses. We recently demonstrated that the expression of proinflammatory cytokines and chemokines is reduced in COX-1 null ((-/-)), and increased in COX-2(-/-) mice compared with their respective wild type controls during lipopolysaccharide (LPS)-induced innate immune activation. As chemokines are involved in leukocyte recruitment into the inflamed brain, we hypothesized that COX-1 and COX-2 deletion will differentially modulate blood-brain barrier (BBB) permeability in response to LPS. In the present study, using quantitative magnetic resonance imaging, we found that LPS-induced BBB disruption was exacerbated in COX-2(-/-) versus COX-2(+/+) mice. In the hippocampus and cortex of LPS-treated mice, matrix metalloproteinase (MMP)-3 activity was significantly decreased in COX-1(-/-) mice, whereas in COX-2(-/-) mice the activity of both MMP-9 and MMP-3, known to mediate BBB breakdown, was increased. Brain mRNA expression of the leukocyte attracting chemokine Cxcl10, the intercellular interaction molecule Icam-1, the pan-leukocyte marker Cd45 was increased in COX-2(-/-) versus COX-2(+/+) mice, whereas Cxcl10 and Cd45 mRNA expression was decreased in COX-1(-/-) versus COX-1(+/+) mice after LPS. Altogether, these results indicate that COX-2 activity modulates MMP-9 and-3 activities and is necessary to maintain BBB integrity during toll-like receptor 4-dependent innate immune activation.

Indexed as

AnimalsBlood-Brain BarrierCapillary PermeabilityCyclooxygenase 1Cyclooxygenase 2Fluorescence Resonance Energy TransferGene ExpressionHippocampusInflammationInjections, IntraventricularLipopolysaccharidesMagnetic Resonance ImagingMatrix Metalloproteinase 3Matrix Metalloproteinase 9MiceMice, KnockoutCyclooxygenase 1Cyclooxygenase 2LipopolysaccharidesMatrix Metalloproteinase 3Matrix Metalloproteinase 9

Identifiers

PMID19844242
PMCPMC2818570
OpenAlexW2012829023

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.