Evidence map›Paper›PMID 18790542›Full record

ReviewTrends in pharmacological sciences2008

Addictive drugs modulate GIRK-channel signaling by regulating RGS proteins.

Marta Lomazzi, Paul A Slesinger, Christian Lüscher

Open access · greenAbstract readReview
In one paragraph

Review in Trends in pharmacological sciences, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

20 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Mechanisms of cannabinoid CBEBioMedicine · 2019
    Article
  4. Acute and subchronic PCP attenuate D2 autoreceptor signaling in substantia nigra dopamine neurons.European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology · 2019
    Article
  5. Article
  6. Article
  7. Article
  8. A KCNJ6 gene polymorphism modulates theta oscillations during reward processing.International journal of psychophysiology : official journal of the International Organization of Psychophysiology · 2017
    Article
  9. Review
  10. Article
  11. Article
  12. GIRK channel modulation by assembly with allosterically regulated RGS proteins.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
  13. Aberrant dopamine D2-like receptor function in a rodent model of schizophrenia.The Journal of pharmacology and experimental therapeutics · 2012
    Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Review
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 2 countries.

Marta LomazziDepartment of Basic Neurosciences, Medical Faculty, University of Geneva, 1, Michel-Servet, CH-1211 Geneva, Switzerland.
Paul A Slesinger
Christian Lüscher
University of Geneva · CHSalk Institute for Biological Studies · US

Funding

Kir 3 Channel Subunits in Drug Abuse with GABAB AgonistsR01DA019022 · NIDA · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI SLESINGER, PAUL A · 2006 to 2010
$2.3M
NIDA NIH HHS 5R01-DA019022NIDA NIH HHS R01 DA019022
6 · The paper itself

Abstract

Regulator of G-protein signaling (RGS) proteins are strong modulators of G-protein-mediated pathways in the nervous system. One function of RGS proteins is to accelerate the activation-deactivation kinetics of G-protein-coupled inwardly rectifying potassium (GIRK) channels. The opening of GIRK channels reduces the firing rates of neurons. Recent studies indicate that RGS proteins also modulate the coupling efficiency between gamma-aminobutyric acid type B (GABA(B)) receptors and GIRK channels in dopamine neurons of the ventral tegmental area (VTA), the initial target for addictive drugs in the brain reward pathway. Chronic drug exposure can dynamically regulate the expression levels of RGS. Functional and behavioral studies now reveal that levels of RGS2 protein, through selective association with GIRK3, critically determine whether GABA(B) agonists are excitatory or inhibitory in the VTA. The regulation of RGS protein in the reward pathway might underlie adaptation to different types of addictive drugs.

Indexed as

AnimalsG Protein-Coupled Inwardly-Rectifying Potassium ChannelsGTP-Binding Protein RegulatorsHumansSignal TransductionSubstance-Related DisordersG Protein-Coupled Inwardly-Rectifying Potassium ChannelsGTP-Binding Protein Regulators

Identifiers

PMID18790542
PMCPMC2818288
OpenAlexW1982373294

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.