Evidence map›Paper›PMID 18511205›Full record

ArticleNeuroscience2008

Apocynin improves outcome in experimental stroke with a narrow dose range.

X N Tang, B Cairns, N Cairns, M A Yenari

Open access · greenAbstract read
In one paragraph

Article in Neuroscience, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed, 1 pooled it
9.9field-weighted citation impact, top 2% 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

83 citing papers in PubMed, 1 synthesis or guideline pooled it, 143 citations in OpenAlex.

  1. Pooled it
  2. Article
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  5. Review
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  7. NADExperimental neurology · 2020
    Review
  8. Article
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  13. A combination antioxidant therapy to inhibit NOX2 and activate Nrf2 decreases secondary brain damage and improves functional recovery after traumatic brain injury.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2018
    Article
  14. Review
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23 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 1 country.

X N TangDepartment of Neurology, University of California, San Francisco and San Francisco Veterans Affairs Medical Center, San Francisco, CA 94121, USA.
B Cairns
N Cairns
M A Yenari
Stanford University · USUniversity of California, San Francisco · US

Funding

Transgenic animal injury paradigmsP01NS037520 · NINDS · STANFORD UNIVERSITY · PI STEINBERG, GARY K · 1999 to 2008
$10.8M
Transgenic Animal CoreP50NS014543 · NINDS · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI GIFFARD, RONA G · 1990 to 2007
$8.2M
Transgenic Animal CoreP01NS014543 · NINDS · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI CHAN, PAK H · 1985 to 2011
$4.7M
Inflammatory Mechanisms in Cerebral IschemiaR01NS040516 · NINDS · STANFORD UNIVERSITY · PI YENARI, MIDORI A · 2001 to 2014
$4.6M
NINDS NIH HHS P01 NS014543NINDS NIH HHS P01 NS037520NINDS NIH HHS P01NS37520NINDS NIH HHS P50 NS014543NINDS NIH HHS R01 NS040516NINDS NIH HHS R01 NS40516
6 · The paper itself

Abstract

Inflammation following ischemic stroke is known to contribute to injury. NADPH oxidase (NOX) is a major enzyme system originally studied in immune cells that leads to superoxide (O.*) generation. Apocynin is a NOX inhibitor that has been studied as a potential treatment in experimental stroke. Here we explored the effect of different doses of apocynin in a mouse model of 2 h transient middle cerebral artery occlusion (tMCAO) followed by 22 h reperfusion. Apocynin, given i.v. at a dose of 2.5 mg/kg 30 min before reperfusion, improved neurological function (P<0.01), reduced infarct volume (P<0.05), and reduced the incidence of cerebral hemorrhage (P<0.05), but not at higher doses of 3.75 and 5 mg/kg, where it actually increased brain hemorrhage. Apocynin also tended to reduce mortality at the lower dose, but not at higher doses. Using hydroethine fluorescence to delineate O.* in the brain, neurons and some microglia/macrophages, but not vascular endothelial cells were found to contain O.*. Apocynin at protective doses markedly prevented ischemia-induced increases in O.*. Our data suggested that apocynin can protect against experimental stroke, but with a narrow therapeutic window.

Indexed as

Neuroprotective AgentsAcetophenonesAnimalsBehavior, AnimalBlood-Brain BarrierCD11b AntigenCerebral InfarctionDNA-Binding ProteinsDose-Response Relationship, DrugEnzyme InhibitorsIntracranial HemorrhagesMacrophagesMaleMiceMice, Inbred C57BLMicrogliaAcetophenonesacetovanilloneCD11b AntigenDNA-Binding ProteinsEnzyme InhibitorsNADPH OxidasesNerve Tissue ProteinsNeuN protein, mouseNeuroprotective AgentsNuclear ProteinsPlatelet Endothelial Cell Adhesion Molecule-1Superoxides

Identifiers

PMID18511205
PMCPMC2518451
OpenAlexW2027029889

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.