Evidence map›Paper›PMID 21054387›Full record

ArticleJournal of neurochemistry2011

Delayed treatment with a novel neurotrophic compound reduces behavioral deficits in rabbit ischemic stroke.

Paul A Lapchak, David R Schubert, Pamela A Maher

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Journal of neurochemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.7field-weighted citation impact, top 8% 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

23 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. The Nrf2 Pathway in Ischemic Stroke: A Review.Molecules (Basel, Switzerland) · 2021
    Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Back to the future with phenotypic screening.ACS chemical neuroscience · 2014
    Review
  12. Novel curcumin derivative CNB-001 mitigates obesity-associated insulin resistance.The Journal of pharmacology and experimental therapeutics · 2014
    Article
  13. Review
  14. Article
  15. Review
  16. Three variations in rabbit angiographic stroke models.Journal of neuroscience methods · 2013
    Article
  17. Article
  18. Clinical neuroprotective drugs for treatment and prevention of stroke.International journal of molecular sciences · 2012
    Review
  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

3 authors at 2 institutions in 1 country.

Paul A LapchakCedars-Sinai Medical Center, Department of Neurology, Burns and Allen Research Institute, Los Angeles, California, USA.
David R Schubert
Pamela A Maher
Salk Institute for Biological Studies · USCedars-Sinai Medical Center · US

Funding

Phenylpropanoid Analogs to Treat StrokeU01NS060685 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LAPCHAK, PAUL A · 2009 to 2014
$2.9M
A Novel Family of Neuroprotective Compounds for StrokeR01NS060864 · NINDS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI SCHUBERT, DAVID R · 2009 to 2010
$1.6M
NINDS NIH HHS 1 R01 NS060864-01NINDS NIH HHS R01 NS060864NINDS NIH HHS U01 NS060685NINDS NIH HHS U01 NS60685-01
6 · The paper itself

Abstract

Acute ischemic stroke is a major risk for morbidity and mortality in our aging population. Currently only one drug, the thrombolytic tissue plasminogen activator, is approved by the US Food and Drug Administration to treat stroke. Therefore, there is a need to develop new drugs that promote neuronal survival following stroke. We have synthesized a novel neuroprotective molecule called CNB-001 (a pyrazole derivative of curcumin) that has neurotrophic activity, enhances memory, and blocks cell death in multiple toxicity assays related to ischemic stroke. In this study, we tested the efficacy of CNB-001 in a rigorous rabbit ischemic stroke model and determined the molecular basis of its in vivo activity. CNB-001 has substantial beneficial properties in an in vitro ischemia assay and improves the behavioral outcome of rabbit ischemic stroke even when administered 1 h after the insult, a therapeutic window in this model comparable to tissue plasminogen activator. In addition, we elucidated the protein kinase pathways involved in neuroprotection. CNB-001 maintains the calcium-calmodulin-dependent kinase signaling pathways associated with neurotrophic growth factors that are critical for the maintenance of neuronal function. On the basis of its in vivo efficacy and novel mode of action, we conclude that CNB-001 has a great potential for the treatment of ischemic stroke as well as other CNS pathologies.

Indexed as

Disease Models, AnimalAnimalsBrain IschemiaCells, CulturedCurcuminMaleMiceMice, Inbred BALB CMotor ActivityNeuroprotective AgentsPyrazolesRabbitsStrokeTime FactorsTreatment OutcomeCNB 001CurcuminNeuroprotective AgentsPyrazoles

Identifiers

PMID21054387
PMCPMC3004475
OpenAlexW1942718624

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.