Evidence map›Paper›PMID 19255856›Full record

ReviewJournal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology2009

Modulation of cannabinoid receptor activation as a neuroprotective strategy for EAE and stroke.

Ming Zhang, Billy R Martin, Martin W Adler, Raj J Razdan, Weimin Kong, Doina Ganea, Ronald F Tuma

Open access · greenAbstract readReview
In one paragraph

Review in Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 1 pooled it
8.0field-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

61 citing papers in PubMed, 1 synthesis or guideline pooled it, 101 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Cannabinoid-Based Medicines and Multiple Sclerosis.Advances in experimental medicine and biology · 2021
    Review
  16. Review
  17. Article
  18. Review
  19. Review
  20. Review

1 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

7 authors at 3 institutions in 1 country.

Ming ZhangCenter for Substance Abuse Research, Temple University School of Medicine, Philadelphia, PA 19140, USA.
Billy R Martin
Martin W Adler
Raj J Razdan
Weimin Kong
Doina Ganea
Ronald F Tuma
Temple University · USOrganix (United States) · USVirginia Commonwealth University · US

Funding

Pilot Projects Core (PPC)P30DA013429 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI Munir Gunes Kutlu · 2000 to 2026
$34.6M
THC RECEPTORSR01DA003672 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI WILEY, JENNY L. · 1985 to 2018
$4.9M
SYNTHESIS OF TETRAHYDROCANNABINOL RELATED COMPOUNDSR01DA005488 · NIDA · ORGANIX, INC. · PI MAHADEVAN, ANURADHA · 1988 to 2011
$4.1M
THC RECEPTORSR37DA003672 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI MARTIN, BILLY R · 1997 to 2006
$2.8M
CB2 Receptor Regulatin of Inflammatory Response in EAER01AI084065 · NIAID · TEMPLE UNIV OF THE COMMONWEALTH · PI GANEA, DOINA, TUMA, RONALD F · 2009 to 2012
$1.5M
NIAID NIH HHS R01 AI084065NIDA NIH HHS DA 03672NIDA NIH HHS DA 05488NIDA NIH HHS DA P30 13429NIDA NIH HHS R01 DA003672NIDA NIH HHS R01 DA005488NIDA NIH HHS R37 DA003672
6 · The paper itself

Abstract

Recognition of the importance of the endocannabinoid system in both homeostasis and pathologic responses raised interest recently in the development of therapeutic agents based on this system. The CB(2) receptor, a component of the endocannabinoid system, has significant influence on immune function and inflammatory responses. Inflammatory responses are major contributors to central nervous system (CNS) injury in a variety of diseases. In this report, we present evidence that activation of CB(2) receptors, by selective CB(2) agonists, reduces inflammatory responses that contribute to CNS injury. The studies demonstrate neuroprotective effects in experimental autoimmune encephalomyelitis, a model of multiple sclerosis, and in a murine model of cerebral ischemia/reperfusion injury. In both cases, CB(2) receptor activation results in reduced white cell rolling and adhesion to cerebral microvessels, a reduction in immune cell invasion, and improved neurologic function after insult. In addition, administration of the CB(1) antagonist SR141716A reduces infarct size following ischemia/reperfusion injury. Administration of both a selective CB(2) agonist and a CB(1) antagonist has the unique property of increasing blood flow to the brain during the occlusion period, suggesting an effect on collateral blood flow. In summary, selective CB(2) receptor agonists and CB(1) receptor antagonists have significant potential for neuroprotection in animal models of two devastating diseases that currently lack effective treatment options.

Indexed as

AnimalsEncephalomyelitis, Autoimmune, ExperimentalHumansNeuroprotective AgentsReceptors, CannabinoidStrokeNeuroprotective AgentsReceptors, Cannabinoid

Identifiers

PMID19255856
PMCPMC2855650
OpenAlexW2066681847

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.