Evidence map›Paper›PMID 30483131›Full record

ReviewFrontiers in pharmacology2018

The Role of G-proteins and G-protein Regulating Proteins in Depressive Disorders.

Nicolas B Senese, Mark M Rasenick, John R Traynor

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in pharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Novel Molecular Targets of Antidepressants.Molecules (Basel, Switzerland) · 2022
    Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Antidepressants Produce Persistent GMolecular pharmacology · 2021
    Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  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 3 institutions in 1 country.

Nicolas B SeneseDepartment of Physiology and Biophysics, University of Illinois at Chicago, Chicago, IL, United States.
Mark M RasenickDepartment of Physiology and Biophysics, University of Illinois at Chicago, Chicago, IL, United States.
John R TraynorDepartment of Pharmacology and Edward F. Domino Research Center, University of Michigan, Ann Arbor, MI, United States.
Jesse Brown VA Medical Center · USUniversity of Illinois Chicago · USUniversity of Michigan–Ann Arbor · US

Funding

Regulator of G protein signaling proteins differentially control opioid analgesiaR01DA035316 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TRAYNOR, JOHN R. · 2014 to 2018
$2.7M
Mechanism of Action for n-3 PUFA antidepressant propertiesR01AT009169 · NCCIH · UNIVERSITY OF ILLINOIS AT CHICAGO · PI RASENICK, MARK M. · 2015 to 2018
$1.5M
RGS modulation of 5HT1A receptor signaling in depressionR21MH097012 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TRAYNOR, JOHN R. · 2012 to 2013
$418k
Lipid raft localization of Gs: a biomarker for depression and therapeutic responseI01BX001149 · VA · JESSE BROWN VA MEDICAL CENTER · PI RASENICK, MARK M. · 2012 to 2024
–
BLRD Research Career Scientist Award ApplicationIK6BX004475 · VA · JESSE BROWN VA MEDICAL CENTER · PI MARK M. RASENICK · 2019 to 2026
–
BLRD VA I01 BX001149BLRD VA IK6 BX004475NCCIH NIH HHS R01 AT009169NIDA NIH HHS R01 DA035316NIMH NIH HHS R21 MH097012
6 · The paper itself

Abstract

Progress toward new antidepressant therapies has been relatively slow over the past few decades, with the result that individuals suffering from depression often struggle to find an effective treatment - a process often requiring months. Furthermore, the neural factors that contribute to depression remain poorly understood, and there are many open questions regarding the mechanism of action of existing antidepressants. A better understanding of the molecular processes that underlie depression and contribute to antidepressant efficacy is therefore badly needed. In this review we highlight research investigating the role of G-proteins and the regulators of G-protein signaling (RGS) proteins, two protein families that are intimately involved in both the genesis of depressive states and the action of antidepressant drugs. Many antidepressants are known to indirectly affect the function of these proteins. Conversely, dysfunction of the G-protein and RGS systems can affect antidepressant efficacy. However, a great deal remains unknown about how these proteins interact with antidepressants. Findings pertinent to each individual G-protein and RGS protein are summarized from

Indexed as

antidepressantdepressionGPCRG-proteinRGS

Identifiers

PMID30483131
PMCPMC6244039
OpenAlexW2901795016

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.