Evidence map›Paper›PMID 25164674›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

Fast phasic release properties of dopamine studied with a channel biosensor.

Geraldine J Kress, Hong-Jin Shu, Andrew Yu, Amanda Taylor, Ann Benz, Steve Harmon, Steven Mennerick

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Spatial and temporal scales of dopamine transmission.Nature reviews. Neuroscience · 2021
    Review
  4. Review
  5. Mechanisms and regulation of dopamine release.Current opinion in neurobiology · 2019
    Review
  6. Article
  7. Article
  8. Cholinergic Interneurons Underlie Spontaneous Dopamine Release in Nucleus Accumbens.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  9. Article
  10. Article
  11. Mechanisms and functions of GABA co-release.Nature reviews. Neuroscience · 2016
    Review
  12. Dopamine directly modulates GABAA receptors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  13. Carbon nanotube biosensors.Frontiers in chemistry · 2015
    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

7 authors at 1 institution in 1 country.

Geraldine J KressDepartments of Psychiatry and.
Hong-Jin ShuDepartments of Psychiatry and.
Andrew YuDepartments of Psychiatry and.
Amanda TaylorDepartments of Psychiatry and.
Ann BenzDepartments of Psychiatry and.
Steve HarmonAnatomy and Neurobiology and.
Steven MennerickDepartments of Psychiatry and Anatomy and Neurobiology and Taylor Family Institute for Innovative Psychiatric Research, Washington University School of Medicine, St. Louis, Missouri 63110 menneris@wustl.edu.
Institute of Neurobiology · BG

Funding

BIOMEDICAL RESEARCH TRAINING IN DRUG ABUSET32DA007261 · NIDA · WASHINGTON UNIVERSITY · PI ARPANA AGRAWAL, Jose A Moron-Concepcion · 1991 to 2026
$8.8M
NICOTINIC MODULATION OF DOPAMINE RELEASE STUDIED WITH A CHANNEL-BASED BIOSENSORR21DA032915 · NIDA · WASHINGTON UNIVERSITY · PI MENNERICK, STEVEN J · 2012 to 2013
$410k
NIDA NIH HHS R21 DA032915NIDA NIH HHS R21DA032915NIDA NIH HHS T32 DA007261NIDA NIH HHS T32DA007261
6 · The paper itself

Abstract

Few other neurotransmitters are of as intense interest to neuropsychiatry and neurology as dopamine, yet existing techniques to monitor dopamine release leave an important spatiotemporal gap in our understanding. Electrochemistry and fluorescence imaging tools have been developed to fill the gap, but these methods have important limitations. We circumvent these limitations by introducing a dopamine-gated chloride channel into rat dorsal striatal medium spiny neurons, targets of strong dopamine innervation, thereby transforming dopamine from a slow transmitter into a fast transmitter and revealing new opportunities for studying moment-to-moment regulation of dopamine release. We demonstrate pharmacological and biophysical properties of the channel that make it suitable for fast, local dopamine measurements, and we demonstrate for the first time spontaneous and evoked responses to vesicular dopamine release in the dorsal striatum. Evoked dopamine currents were separated into a fast, monosynaptic component and a slower-rising and decaying disynaptic component mediated by nicotinic receptor activation. In summary, LGC-53 represents a dopamine biosensor with properties suitable for temporal separation of distinct dopamine signals in targets of dopamine innervation.

Indexed as

AnimalsBiosensing TechniquesCaenorhabditis elegansCell LineChloride ChannelsCorpus StriatumDopamineHumansLigand-Gated Ion ChannelsNeuronsPatch-Clamp TechniquesRatsXenopusChloride ChannelsDopamineLigand-Gated Ion Channelsdopamine releaseligand-gated ion channelnicotinicpresynapticstriatum

Identifiers

PMID25164674
PMCPMC4145179
OpenAlexW2015648917

What OpenQuestion holds

Textmetadata
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.