Evidence map›Paper›PMID 34348146›Full record

ArticleCell reports2021

The residence of synaptically released dopamine on D2 autoreceptors.

Alec F Condon, Brooks G Robinson, Naeem Asad, Timothy M Dore, Lin Tian, John T Williams

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2021. 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
1.9field-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, 29 citations in OpenAlex.

  1. The Synaptic Vesicle Priming Protein Munc13 Mediates Evoked Somatodendritic Dopamine Release.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
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  13. Synaptotagmin-1 is a CaCell reports · 2023
    Article
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  18. A fluorescent nanosensor paint detects dopamine release at axonal varicosities with high spatiotemporal resolution.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
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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

6 authors at 4 institutions in 2 countries.

Alec F CondonThe Vollum Institute, Oregon Health Sciences University, Portland, OR, USA.
Brooks G RobinsonThe Vollum Institute, Oregon Health Sciences University, Portland, OR, USA.
Naeem AsadNew York University Abu Dhabi, Saadiyat Island, P.O. Box 129188, Abu Dhabi, United Arab Emirates.
Timothy M DoreNew York University Abu Dhabi, Saadiyat Island, P.O. Box 129188, Abu Dhabi, United Arab Emirates.
Lin TianDepartment of Biochemistry and Molecular Medicine, School of Medicine, University of California, Davis, Davis, CA, USA.
John T WilliamsThe Vollum Institute, Oregon Health Sciences University, Portland, OR, USA. Electronic address: williamj@ohsu.edu.
New York University Abu Dhabi · AEVollum Institute · USOregon Health & Science University · USUniversity of California, Davis · US

Funding

BIOLOGICAL BASES OF DRUG-SEEKING BEHAVIORT32DA007262 · NIDA · OREGON HEALTH & SCIENCE UNIVERSITY · PI WILLIAMS, JOHN T · 1991 to 2022
$9.4M
COCAINE: EFFECTS ON SINGLE NEURONSR01DA004523 · NIDA · OREGON HEALTH & SCIENCE UNIVERSITY · PI WILLIAMS, JOHN T · 1987 to 2025
$7.6M
Multiplex interrogation of neuromodulatory signaling in behaving animals with enhanced depth and resolutionU01NS120820 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI TIAN, LIN, VONZASTROW, MARK E · 2021 to 2024
$3.5M
Genetically encoded indicators for large-scale sensing of neuromodulatory signaling in behaving animalsU01NS103522 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI NIMMERJAHN, AXEL, TIAN, LIN · 2017 to 2019
$2.9M
Cocaine-induced plasticity of D2 receptor synapsesK99DA044287 · NIDA · OREGON HEALTH & SCIENCE UNIVERSITY · PI ROBINSON, BROOKS G · 2018 to 2019
$162k
Desensitization and recovery of D2 autoreceptorsF31DA047007 · NIDA · OREGON HEALTH & SCIENCE UNIVERSITY · PI CONDON, ALEC · 2018 to 2020
$135k
NIDA NIH HHS F31 DA047007NIDA NIH HHS K99 DA044287NIDA NIH HHS R01 DA004523NIDA NIH HHS T32 DA007262NINDS NIH HHS U01 NS103522NINDS NIH HHS U01 NS120820
6 · The paper itself

Abstract

Neuromodulation mediated by synaptically released endogenous transmitters acting in G-protein-coupled receptors (GPCRs) is slow primarily because of multistep downstream signaling. What is less well understood is the spatial and temporal kinetics of transmitter and receptor interaction. The present work uses the combination of the dopamine sensor, dLight, to detect the spatial release and diffusion of dopamine and a caged form of a D2-dopamine receptor antagonist, CyHQ-sulpiride, to rapidly block the D2 autoreceptors. Photoactivation of the CyHQ-sulpiride blocks receptors in milliseconds such that the time course of dopamine/receptor interaction is mapped onto the downstream signaling. The results show that highly localized release, but not dopamine diffusion, defines the time course of the functional interaction between dopamine and D2 autoreceptors, which determines downstream inhibition.

Indexed as

AnimalsDopamineExtracellular SpaceFemaleG Protein-Coupled Inwardly-Rectifying Potassium ChannelsKineticsLightMaleMiceMice, Inbred C57BLPhotolysisReceptors, Dopamine D2SynapsesTime FactorsDopamineG Protein-Coupled Inwardly-Rectifying Potassium ChannelsReceptors, Dopamine D2caged-sulpiridedendritic releaseGIRKG Protein Coupled ReceptorsSubstantia Nigra

Identifiers

PMID34348146
PMCPMC8351352
OpenAlexW3191386967

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.