Evidence map›Paper›PMID 20590557›Full record

ReviewBritish journal of pharmacology2010

Cannabinoid CB1 receptor-interacting proteins: novel targets for central nervous system drug discovery?

Tricia H Smith, Laura J Sim-Selley, Dana E Selley

Open access · bronzeAbstract readReview
In one paragraph

Review in British journal of pharmacology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
8.9field-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

63 citing papers in PubMed, 116 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Cannabinoids: Therapeutic Use in Clinical Practice.International journal of molecular sciences · 2022
    Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Review

3 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 1 institution in 1 country.

Tricia H SmithDepartment of Pharmacology and Toxicology, Virginia Commonwealth University, School of Medicine, MCV Campus, Richmond, VA 23298-0524, USA.
Laura J Sim-Selley
Dana E Selley
Virginia Commonwealth University · US

Funding

Brain Cannabinoid Signaling: Selectivity and AdaptationR01DA014277 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI SIM-SELLEY, LAURA J · 2002 to 2010
$1.7M
CB1 Receptor Regulation by Cannabinoid Receptor Interacting Protein CRIP1aR21DA025321 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI HOWLETT, ALLYN C, SELLEY, DANA E · 2009 to 2010
$420k
Role of G-gamma-7 in striatal cannabinoid and D2 dopamineR03DA027227 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI SELLEY, DANA E · 2009 to 2010
$150k
Cannabinoid Signaling: Role of Cannabinoid Receptor Interacting Protein (CRIP1a)F31DA023747 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI SMITH, TRICIA HARDT · 2007 to 2009
$64k
NIDA NIH HHS DA014277NIDA NIH HHS DA023747NIDA NIH HHS DA025321NIDA NIH HHS DA027227NIDA NIH HHS F31 DA023747NIDA NIH HHS R01 DA014277NIDA NIH HHS R03 DA027227NIDA NIH HHS R21 DA025321
6 · The paper itself

Abstract

The main pharmacological effects of marijuana, as well as synthetic and endogenous cannabinoids, are mediated through G-protein-coupled receptors (GPCRs), including CB(1) and CB(2) receptors. The CB(1) receptor is the major cannabinoid receptor in the central nervous system and has gained increasing interest as a target for drug discovery for treatment of nausea, cachexia, obesity, pain, spasticity, neurodegenerative diseases and mood and substance abuse disorders. Evidence has accumulated to suggest that CB(1) receptors, like other GPCRs, interact with and are regulated by several other proteins beyond the established role of heterotrimeric G-proteins. These proteins, which include the GPCR kinases, beta-arrestins, GPCR-associated sorting proteins, factor associated with neutral sphingomyelinase, other GPCRs (heterodimerization) and the novel cannabinoid receptor-interacting proteins: CRIP(1a/b), are thought to play important roles in the regulation of intracellular trafficking, desensitization, down-regulation, signal transduction and constitutive activity of CB(1) receptors. This review examines CB(1) receptor-interacting proteins, including heterotrimeric G-proteins, but with particular emphasis on non-G-protein entities, that might comprise the CB(1) receptosomal complex. The evidence for direct interaction with CB(1) receptors and potential functional roles of these interacting proteins is discussed, as are future directions and challenges in this field with an emphasis on the possibility of eventually targeting these proteins for drug discovery.

Indexed as

AnimalsBrainCannabinoid Receptor ModulatorsCannabinoidsCarrier ProteinsDrug Delivery SystemsDrug DiscoveryHumansModels, BiologicalProtein MultimerizationReceptor, Cannabinoid, CB1Receptor Cross-TalkReceptors, G-Protein-CoupledCannabinoid Receptor ModulatorsCannabinoidsCarrier ProteinsCnrip1 protein, ratReceptor, Cannabinoid, CB1Receptors, G-Protein-Coupled

Identifiers

PMID20590557
PMCPMC2931548
OpenAlexW1502369243

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.