Evidence map›Paper›PMID 30176987›Full record

ArticleeLife2018

Manipulating midbrain dopamine neurons and reward-related behaviors with light-controllable nicotinic acetylcholine receptors.

Romain Durand-de Cuttoli, Sarah Mondoloni, Fabio Marti, Damien Lemoine, Claire Nguyen, Jérémie Naudé, Thibaut d'Izarny-Gargas, Stéphanie Pons, Uwe Maskos, Dirk Trauner and 3 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

32 citing papers in PubMed, 65 citations in OpenAlex.

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  16. Article
  17. Molecular photoswitches in aqueous environments.Chemical Society reviews · 2021
    Review
  18. Neurobiology of reward-related learning.Neuroscience and biobehavioral reviews · 2021
    Review
  19. ACS chemical neuroscience · 2020
    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

13 authors at 4 institutions in 2 countries.

Romain Durand-de Cuttoli *Neuroscience Paris Seine - Institut de Biologie Paris Seine (NPS - IBPS), Sorbonne Université, INSERM, CNRS, Paris, France.ORCID 0000-0003-0240-7608
Sarah Mondoloni *Neuroscience Paris Seine - Institut de Biologie Paris Seine (NPS - IBPS), Sorbonne Université, INSERM, CNRS, Paris, France.
Fabio MartiNeuroscience Paris Seine - Institut de Biologie Paris Seine (NPS - IBPS), Sorbonne Université, INSERM, CNRS, Paris, France.
Damien LemoineNeuroscience Paris Seine - Institut de Biologie Paris Seine (NPS - IBPS), Sorbonne Université, INSERM, CNRS, Paris, France.
Claire NguyenNeuroscience Paris Seine - Institut de Biologie Paris Seine (NPS - IBPS), Sorbonne Université, INSERM, CNRS, Paris, France.
Jérémie NaudéNeuroscience Paris Seine - Institut de Biologie Paris Seine (NPS - IBPS), Sorbonne Université, INSERM, CNRS, Paris, France.ORCID 0000-0001-5781-6498
Thibaut d'Izarny-GargasNeuroscience Paris Seine - Institut de Biologie Paris Seine (NPS - IBPS), Sorbonne Université, INSERM, CNRS, Paris, France.ORCID 0000-0002-6084-5836
Stéphanie PonsUnité de Neurobiologie Intégrative des Systèmes Cholinergiques, Department of Neuroscience, Institut Pasteur, Paris, France.ORCID 0000-0003-1027-0621
Uwe MaskosUnité de Neurobiologie Intégrative des Systèmes Cholinergiques, Department of Neuroscience, Institut Pasteur, Paris, France.
Dirk TraunerDepartment of Chemistry, New York University, New York, United States.
Richard H KramerDepartment of Molecular and Cell Biology, University of California Berkeley, Berkeley, United States.
Philippe Faure *Neuroscience Paris Seine - Institut de Biologie Paris Seine (NPS - IBPS), Sorbonne Université, INSERM, CNRS, Paris, France.ORCID 0000-0003-3573-4971
Alexandre Mourot *Neuroscience Paris Seine - Institut de Biologie Paris Seine (NPS - IBPS), Sorbonne Université, INSERM, CNRS, Paris, France.ORCID 0000-0002-8839-7481
Centre National de la Recherche Scientifique · FRInstitut Pasteur · FRLawrence Berkeley National Laboratory · USNew York University · US

Funding

UC Berkeley Vision Science COREP30EY003176 · NEI · UNIVERSITY OF CALIFORNIA BERKELEY · PI RICHARD H KRAMER · 1985 to 2026
$16.4M
Optical Control of Synaptic Transmission for in Vivo Analysis of Brain Circuits and BehaviorU01NS090527 · NINDS · UNIVERSITY OF CALIFORNIA BERKELEY · PI ISACOFF, EHUD, KRAMER, RICHARD H · 2014 to 2016
$2.4M
Probing GABAa receptor function and plasticity with lightR01NS100911 · NINDS · UNIVERSITY OF CALIFORNIA BERKELEY · PI KRAMER, RICHARD H · 2017 to 2020
$1.8M
Agence Nationale de la Recherche ANR-JCJCBrain and Behavior Research Foundation NARSAD Young Investigator GrantDIM Cerveau Pensée PhD fellowshipFédération pour la Recherche sur le Cerveau Rotary Espoir en tête 2012Fondation de France Fondation Medisite fundamental research prizeFondation pour la Recherche Médicale Equipe FRM DEQ2013326488Fondation pour la Recherche Médicale PhD fellowship FDT20170437427Institut National Du Cancer TABAC-16-022Labex Bio-Psy post-doctoral fellowshipNEI NIH HHS P30 EY003176NIH HHS R01-NS100911NIH HHS U01-NS090527NINDS NIH HHS R01 NS100911NINDS NIH HHS U01 NS090527
6 · The paper itself

Abstract

Dopamine (DA) neurons of the ventral tegmental area (VTA) integrate cholinergic inputs to regulate key functions such as motivation and goal-directed behaviors. Yet the temporal dynamic range and mechanism of action of acetylcholine (ACh) on the modulation of VTA circuits and reward-related behaviors are not known. Here, we used a chemical-genetic approach for rapid and precise optical manipulation of nicotinic neurotransmission in VTA neurons in living mice. We provide direct evidence that the ACh tone fine-tunes the firing properties of VTA DA neurons through β2-containing (β2*) nicotinic ACh receptors (nAChRs). Furthermore, locally photo-antagonizing these receptors in the VTA was sufficient to reversibly switch nicotine reinforcement on and off. By enabling control of nicotinic transmission in targeted brain circuits, this technology will help unravel the various physiological functions of nAChRs and may assist in the design of novel therapies relevant to neuropsychiatric disorders.

Indexed as

LightRewardAction PotentialsAnimalsCell LineDopaminergic NeuronsMesencephalonMice, Inbred C57BLNicotineReceptors, NicotinicSignal TransductionVentral Tegmental AreaNicotineReceptors, Nicotinicacetylcholineaddictiondopaminemouseneurosciencenicotineoptogeneticsphotopharmacology

Identifiers

PMID30176987
PMCPMC6122951
OpenAlexW2890434413

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.