Evidence map›Paper›PMID 25716780›Full record

ArticleThe international journal of neuropsychopharmacology2015

Postsynaptic adenosine A2A receptors modulate intrinsic excitability of pyramidal cells in the rat basolateral amygdala.

Andrew R Rau, Olusegun J Ariwodola, Jeff L Weiner

Open access · goldAbstract read
In one paragraph

Article in The international journal of neuropsychopharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.8field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Adenosine ATranslational psychiatry · 2023
    Article
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  5. Review
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  9. Review
  10. Review
  11. Chronic alcohol exposure disrupts CBAddiction biology · 2017
    Article
  12. Adenosine ANeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2016
    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

3 authors at 1 institution in 1 country.

Andrew R RauDepartment of Physiology and Pharmacology, School of Medicine (Mr Rau, Mr Ariwodola, and Dr Weiner), Neuroscience Graduate Program, Graduate School of Arts and Sciences (Mr Rau), Wake Forest University, Winston-Salem, North Carolina.
Olusegun J AriwodolaDepartment of Physiology and Pharmacology, School of Medicine (Mr Rau, Mr Ariwodola, and Dr Weiner), Neuroscience Graduate Program, Graduate School of Arts and Sciences (Mr Rau), Wake Forest University, Winston-Salem, North Carolina.
Jeff L WeinerDepartment of Physiology and Pharmacology, School of Medicine (Mr Rau, Mr Ariwodola, and Dr Weiner), Neuroscience Graduate Program, Graduate School of Arts and Sciences (Mr Rau), Wake Forest University, Winston-Salem, North Carolina. jweiner@wfubmc.edu.
Wake Forest University · US

Funding

Ethanol Mechanisms in GABAAR Gene Targeted MiceR37AA010422 · NIAAA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HOMANICS, GREGG E. · 2010 to 2019
$4.4M
Synaptic Correlates of Vulnerability and Resilience to Alcohol Use DisordersR37AA017531 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI WEINER, JEFFREY L. · 2014 to 2023
$3.5M
Translational Studies on Early-life Stress and Vulnerability to Alcohol AddictionP01AA021099 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI JONES, SARA RAULERSON · 2012 to 2016
$2.8M
Synaptic and Behavioral Correlates of Adeonsinergic Signaling in the BLAF31AA022046 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI RAU, ANDREW RYAN · 2012 to 2014
$121k
NIAAA NIH HHS F31 AA022046NIAAA NIH HHS F31AA022046NIAAA NIH HHS P01 AA021099NIAAA NIH HHS R37 AA010422NIAAA NIH HHS R37AA010422NIAAA NIH HHS R37 AA017531NIAAA NIH HHS R37AA017531
6 · The paper itself

Abstract

backgroundThe basolateral amygdala plays a critical role in the etiology of anxiety disorders and addiction. Pyramidal neurons, the primary output cells of this region, display increased firing following exposure to stressors, and it is thought that this increase in excitability contributes to stress responsivity and the expression of anxiety-like behaviors. However, much remains unknown about the underlying mechanisms that regulate the intrinsic excitability of basolateral amygdala pyramidal neurons.

methodsEx vivo gramicidin perforated patch recordings were conducted in current clamp mode where hyper- and depolarizing current steps were applied to basolateral amygdala pyramidal neurons to assess the effects of adenosine A(2A) receptor modulation on intrinsic excitability.

resultsActivation of adenosine A(2A) receptors with the selective A(2A) receptor agonist CGS-21680 significantly increased the firing rate of basolateral amygdala pyramidal neurons in rat amygdala brain slices, likely via inhibition of the slow afterhyperpolarization potential. Both of these A(2A) receptor-mediated effects were blocked by preapplication of a selective A(2A) receptor antagonist (ZM-241385) or by intra-pipette infusion of a protein kinase A inhibitor, suggesting a postsynaptic locus of A(2A) receptors on basolateral amygdala pyramidal neurons. Interestingly, bath application of the A(2A) receptor antagonist alone significantly attenuated basolateral amygdala pyramidal cell firing, consistent with a role for tonic adenosine in the regulation of the intrinsic excitability of these neurons.

conclusionsCollectively, these data suggest that adenosine, via activation of A(2A) receptors, may directly facilitate basolateral amygdala pyramidal cell output, providing a possible balance for the recently described inhibitory effects of adenosine A1 receptor activation on glutamatergic excitation of basolateral amygdala pyramidal cells.

Indexed as

Synaptic TransmissionAdenosineAdenosine A2 Receptor AgonistsAdenosine A2 Receptor AntagonistsAnimalsBasolateral Nuclear ComplexCyclic AMP-Dependent Protein KinasesExcitatory Postsynaptic PotentialsIn Vitro TechniquesMaleProtein Kinase InhibitorsPyramidal CellsRats, Long-EvansReceptor, Adenosine A2ASynaptic MembranesTime FactorsAdenosineAdenosine A2 Receptor AgonistsAdenosine A2 Receptor AntagonistsCyclic AMP-Dependent Protein KinasesProtein Kinase InhibitorsReceptor, Adenosine A2AA2AadenosineAHPbasolateral amygdalaintrinsic excitability

Identifiers

PMID25716780
PMCPMC4438553
OpenAlexW2070199826

What OpenQuestion holds

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Registered trials

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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.