Evidence map›Paper›PMID 23407950›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2013

Olfactory bulb short axon cell release of GABA and dopamine produces a temporally biphasic inhibition-excitation response in external tufted cells.

Shaolin Liu, Celine Plachez, Zuoyi Shao, Adam Puche, Michael T Shipley

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 94 papers.

0numbers the graph read from it
0cells of the map it votes in
94citing papers in PubMed
6.9field-weighted citation impact, top 2% 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

94 citing papers in PubMed, 131 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Olfactory Bulb DToxins · 2022
    Article
  19. Brief Sensory Deprivation Triggers Cell Type-Specific Structural and Functional Plasticity in Olfactory Bulb Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  20. Review

34 more citing papers are in PubMed but not listed here.

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

5 authors at 1 institution in 1 country.

Shaolin LiuDepartment of Anatomy and Neurobiology, Program in Neuroscience, University of Maryland School of Medicine, Baltimore, Maryland 20201, USA.
Celine Plachez
Zuoyi Shao
Adam Puche
Michael T Shipley
University of Maryland, Baltimore · US

Funding

Olfactory Glomeruli: Cellular and Network MechanismsR01DC005676 · NIDCD · UNIVERSITY OF MARYLAND BALTIMORE · PI SHIPLEY, MICHAEL THOMAS · 2002 to 2017
$5.8M
Supplement to Basal Forebrain Modulation of Olfactory Bulb FunctionR01DC010915 · NIDCD · UNIVERSITY OF MARYLAND BALTIMORE · PI PUCHE, ADAM C · 2011 to 2022
$5.7M
NIDCD NIH HHS DC005676NIDCD NIH HHS DC010915NIDCD NIH HHS R01 DC005676NIDCD NIH HHS R01 DC010915
6 · The paper itself

Abstract

Evidence for coexpression of two or more classic neurotransmitters in neurons has increased, but less is known about cotransmission. Ventral tegmental area (VTA) neurons corelease dopamine (DA), the excitatory transmitter glutamate, and the inhibitory transmitter GABA onto target cells in the striatum. Olfactory bulb (OB) short axon cells (SACs) form interglomerular connections and coexpress markers for DA and GABA. Using an optogenetic approach, we provide evidence that mouse OB SACs release both GABA and DA onto external tufted cells (ETCs) in other glomeruli. Optical activation of channelrhodopsin specifically expressed in DAergic SACs produced a GABA(A) receptor-mediated monosynaptic inhibitory response, followed by DA-D(1)-like receptor-mediated excitatory response in ETCs. The GABA(A) receptor-mediated hyperpolarization activates I(h) current in ETCs; synaptically released DA increases I(h), which enhances postinhibitory rebound spiking. Thus, the opposing actions of synaptically released GABA and DA are functionally integrated by I(h) to generate an inhibition-to-excitation "switch" in ETCs. Consistent with the established role of I(h) in ETC burst firing, we show that endogenous DA release increases ETC spontaneous bursting frequency. ETCs transmit sensory signals to mitral/tufted output neurons and drive intraglomerular inhibition to shape glomerulus output to downstream olfactory networks. GABA and DA cotransmission from SACs to ETCs may play a key role in regulating output coding across the glomerular array.

Indexed as

AnimalsAxonsChannelrhodopsinsDopamineElectric Stimulationgamma-Aminobutyric AcidGlutamate DecarboxylaseHumansImmunohistochemistryJuxtaglomerular ApparatusLasersMiceMice, Inbred C57BLMice, TransgenicNeuronsOlfactory BulbChannelrhodopsinsDopaminegamma-Aminobutyric AcidGlutamate Decarboxylaseglutamate decarboxylase 1Receptors, Dopamine D1Tyrosine 3-Monooxygenase

Identifiers

PMID23407950
PMCPMC3727441
OpenAlexW2004001620

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.