Evidence map›Paper›PMID 22623675›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2012

In vivo visualization of delta opioid receptors upon physiological activation uncovers a distinct internalization profile.

Lauren Faget, Eric Erbs, Julie Le Merrer, Gregory Scherrer, Audrey Matifas, Nadia Benturquia, Florence Noble, Marion Decossas, Marc Koch, Pascal Kessler and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
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  11. Molecular Pharmacology of δ-Opioid Receptors.Pharmacological reviews · 2016
    Review
  12. Article
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  15. Article
  16. Review
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  19. Delta-opioid receptors mediate unique plasticity onto parvalbumin-expressing interneurons in area CA2 of the hippocampus.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    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

14 authors at 5 institutions in 2 countries.

Lauren FagetTranslational Medicine and Neurogenetics, Institut de Génétique et de Biologie Moléculaire et Cellulaire, F-67404 Illkirch, Cedex France.
Eric Erbs
Julie Le Merrer
Gregory Scherrer
Audrey Matifas
Nadia Benturquia
Florence Noble
Marion Decossas
Marc Koch
Pascal Kessler
Jean-Luc Vonesch
Yannick Schwab
Brigitte L Kieffer
Dominique Massotte
Institut de génétique et de biologie moléculaire et cellulaire · FRDélégation Paris 5 · FRInstitut de Biologie Moléculaire des Plantes · FRUniversité Clermont Auvergne · FRUniversité de Bourgogne · FR

Funding

The Role of Striosome Neurons in Mediating Opiod RewardP50DA005010 · NIDA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI FANSELOW, MICHAEL S · 1987 to 2021
$30.7M
NIDA NIH HHS DA-05010NIDA NIH HHS P50 DA005010
6 · The paper itself

Abstract

G-protein-coupled receptors (GPCRs) mediate numerous physiological functions and represent prime therapeutic targets. Receptor trafficking upon agonist stimulation is critical for GPCR function, but examining this process in vivo remains a true challenge. Using knock-in mice expressing functional fluorescent delta opioid receptors under the control of the endogenous promoter, we visualized in vivo internalization of this native GPCR upon physiological stimulation. We developed a paradigm in which animals were made dependent on morphine in a drug-paired context. When re-exposed to this context in a drug-free state, mice showed context-dependent withdrawal signs and activation of the hippocampus. Receptor internalization was transiently detected in a subset of CA1 neurons, uncovering regionally restricted opioid peptide release. Importantly, a pool of surface receptors always remained, which contrasts with the in vivo profile previously established for exogenous drug-induced internalization. Therefore, a distinct response is observed at the receptor level upon a physiological or pharmacological stimulation. Altogether, direct in vivo GPCR visualization enables mapping receptor stimulation promoted by a behavioral challenge and represents a powerful approach to study endogenous GPCR physiology.

Indexed as

Protein TransportAnimalsEnkephalin, MethionineFemaleGene Knock-In TechniquesHippocampusMaleMiceMice, Inbred C57BLMolecular ImagingMorphineReceptors, Opioid, deltaSubstance Withdrawal SyndromeEnkephalin, MethionineMorphineReceptors, Opioid, delta

Identifiers

PMID22623675
PMCPMC3371401
OpenAlexW2087471485

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.