Evidence map›Paper›PMID 21334424›Full record

ArticleNeuroscience2011

Heme oxygenase 1, beneficial role in permanent ischemic stroke and in Gingko biloba (EGb 761) neuroprotection.

Z A Shah, S E Nada, S Doré

Open access · greenAbstract read
In one paragraph

Article in Neuroscience, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed, 2 pooled it
42.1field-weighted citation impact, top 1% 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

65 citing papers in PubMed, 2 syntheses or guidelines pooled it, 137 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Antioxidant Phenylpropanoid Glycosides fromPlants (Basel, Switzerland) · 2021
    Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. The Use of Antioxidants in the Treatment of Migraine.Antioxidants (Basel, Switzerland) · 2020
    Review
  17. Article
  18. Article
  19. Anatomy & cell biology · 2019
    Article
  20. Review

5 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

3 authors at 2 institutions in 1 country.

Z A ShahDepartment of Medicinal and Biological Chemistry, College of Pharmacy and Pharmaceutical Sciences, University of Toledo, Toledo, OH 43614, USA. zahoor.shah@utoledo.edu
S E Nada
S Doré
University of Toledo · USJohns Hopkins Medicine · US

Funding

Neuroprotective Effect of Ginkgo Biloba and its Bioactive Components IschemiaR00AT004197 · NCCIH · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI SHAH, ZAHOOR AHMAD · 2010 to 2012
$737k
Effect of Flavanol-Rich Cocoa Extract in Acute Neurodegenerative ConditionsR21AT005085 · NCCIH · UNIVERSITY OF FLORIDA · PI DORE, SYLVAIN · 2010 to 2011
$423k
Neuroprotective mechanisms of EGb-761R21AT001836 · NCCIH · JOHNS HOPKINS UNIVERSITY · PI DORE, SYLVAIN · 2004 to 2005
$409k
Neuroprotective Effect of Ginkgo Biloba and its Bioactive Components IschemiaK99AT004197 · NCCIH · JOHNS HOPKINS UNIVERSITY · PI SHAH, ZAHOOR AHMAD · 2008 to 2009
$177k
NCCIH NIH HHS K99 AT004197NCCIH NIH HHS K99AT004197NCCIH NIH HHS R00 AT004197NCCIH NIH HHS R21 AT001836NCCIH NIH HHS R21AT001836NCCIH NIH HHS R21 AT005085NCCIH NIH HHS R21AT005085
6 · The paper itself

Abstract

Ginkgo biloba extract, EGb 761, a popular and standardized natural extract, contains 24% ginkgo-flavonol glycosides and 6% terpene lactones. EGb 761 is used worldwide to treat many ailments, and although a number of studies have shown its neuroprotective properties, the mechanisms of action have not been elucidated fully. We hypothesize that EGb 761 and some of its bioactive components [Bilobalide (BB), Ginkgolide A (GA), Ginkgolide B (GB), and Terpene Free Material (TFM)] could provide neuroprotection in ischemic conditions through heme oxygenase 1 (HO1). Mice were subjected to permanent distal middle cerebral artery occlusion (pMCAO) and survived for 7 days. HO1 knockout (HO1⁻/⁻) mice showed significantly higher (P<0.05) infarct volume and Neurologic Deficit Scores (NDS) as compared to their wildtype (WT) counterparts. In another cohort, WT mice subjected to pMCAO and treated at 4 h of pMCAO with 100 mg/kg EGb 761, 6 mg/kg BB, GA, GB, or 10 mg/kg TFM showed significantly lower (P<0.05) infarct volumes (BB; 29.0±3.9%, GA; 31.3±4.0%, GB; 32.0±3.8%, TFM; 32.5±3.5%, and EGb 761; 27.4±4.5%) than those in the vehicle-treated mice (46.0±3.7%). Similarly, NDS were lower in BB; 7.1±1.8, GA; 7.4±2.1, GB; 7.9±1.8, TFM; 7.7±1.7, and EGb 761; 6.8±2.0 groups as compared with the vehicle-treated group (13.8±1.5). Interestingly, the protective effect of EGb 761 was essentially lost when HO1 knockout mice were treated with EGb 761. In another cohort, HO1, vascular endothelial growth factor (VEGF) and endothelial nitric oxide synthase (eNOS) protein levels in the brain cortices appeared to be higher in EGb 761 and BB but not in GA, GB and TFM treated groups. Together, these results suggest that HO1 plays, at least in part, an important role in the neuroprotective mechanism of EGb 761 and in delayed ischemia. Targeting this pathway could lead to neuroprotective agents against ischemic stroke.

Indexed as

AnimalsBlotting, WesternGinkgo bilobaHeme Oxygenase-1MiceMice, Inbred C57BLMice, KnockoutNeuroprotective AgentsPlant ExtractsStrokeHeme Oxygenase-1Neuroprotective AgentsPlant Extracts

Identifiers

PMID21334424
PMCPMC3070771
OpenAlexW2045609579

What OpenQuestion holds

Textmetadata
LicenceTDM
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.