Evidence map›Paper›PMID 23040803›Full record

ReviewNeuron2012

Orphan GPCRs and neuromodulation.

Olivier Civelli

Abstract readReview
In one paragraph

Review in Neuron, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
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

29 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. The role of orphan receptor GPR139 in neuropsychiatric behavior.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
    Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. GFrontiers in aging neuroscience · 2019
    Review
  18. Article
  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

1 author.

Olivier CivelliDepartment of Pharmacology, University of California, Irvine, Irvine, CA 92697-4625, USA. ocivelli@uci.edu

Funding

CHARACTERIZATION OF TWO NOVEL NEUROPEPTIDESR01MH060231 · NIMH · UNIVERSITY OF CALIFORNIA-IRVINE · PI CIVELLI, OLIVIER · 1999 to 2008
$2.7M
A novel neuropeptide system involved in drug abuseR01DA024746 · NIDA · UNIVERSITY OF CALIFORNIA-IRVINE · PI CIVELLI, OLIVIER · 2010 to 2013
$1.5M
Novel Glycoprotein Hormone-Like proteinsR01DK063001 · NIDDK · UNIVERSITY OF CALIFORNIA-IRVINE · PI CIVELLI, OLIVIER · 2003 to 2006
$1.2M
NIDA NIH HHS DA024746NIDA NIH HHS R01 DA024746NIDDK NIH HHS R01 DK063001NIMH NIH HHS MH60231NIMH NIH HHS R01 MH060231
6 · The paper itself

Abstract

Most G protein-coupled receptors (GPCRs) started as orphan GPCRs. Matching them to known neuromodulators led to the elucidation of the broad diversity of the neuroreceptor families. Moreover, orphan GPCRs have also been used as targets to discover novel neuromodulators. These discoveries have had profound impact on our understanding of brain function. Here, I present an overview of how some of the novel neuropeptides have enlarged our comprehension of responses that direct sleep/wakefulness, the onset of obesity and the feeding response. I also discuss other advances gained from orphan GPCR studies such as the concept of specificity in neuromodulation or of receptors acting as sensors instead of synaptic transmitters. Finally, I suggest that the recently discovered neuromodulators may hold the keys to our understanding of higher brain functions and psychiatric disorders.

Indexed as

AnimalsBrainHumansNeurotransmitter AgentsReceptors, G-Protein-CoupledNeurotransmitter AgentsReceptors, G-Protein-Coupled

Identifiers

PMID23040803
PMCPMC3474844

What OpenQuestion holds

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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.