Evidence map›Paper›PMID 24355495›Full record

ArticleNeuroscience2014

Modulation of synaptic transmission by adenosine in layer 2/3 of the rat visual cortex in vitro.

N M Bannon, P Zhang, V Ilin, M Chistiakova, M Volgushev

Abstract read
In one paragraph

Article in Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 27% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Feedback facilitation by adenosine APurinergic signalling · 2024
    Article
  3. Adenosinergic Modulation of Layer 6 Microcircuitry in the Medial Prefrontal Cortex Is Specific to Presynaptic Cell Type.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  4. Adenosine ABiomolecules · 2023
    Article
  5. Altered Heterosynaptic Plasticity Impairs Visual Discrimination Learning in Adenosine A1 Receptor Knock-Out Mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  6. Article
  7. Distinct Heterosynaptic Plasticity in Fast Spiking and Non-Fast-Spiking Inhibitory Neurons in Rat Visual Cortex.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  8. Article
  9. Review
  10. Article
  11. Adenosine Shifts Plasticity Regimes between Associative and Homeostatic by Modulating Heterosynaptic Changes.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  12. Article
  13. Article
  14. Homeostatic role of heterosynaptic plasticity: models and experiments.Frontiers in computational neuroscience · 2015
    Review
  15. 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

5 authors at 1 institution in 1 country.

N M BannonDepartment of Psychology, University of Connecticut, Storrs, CT 06269, USA. Electronic address: nicholas.bannon@uconn.edu.
P ZhangDepartment of Psychology, University of Connecticut, Storrs, CT 06269, USA. Electronic address: pei.zhang@huskymail.uconn.edu.
V IlinDepartment of Psychology, University of Connecticut, Storrs, CT 06269, USA. Electronic address: vladimir.ilin@uconn.edu.
M ChistiakovaDepartment of Psychology, University of Connecticut, Storrs, CT 06269, USA. Electronic address: chistyakovam@gmail.com.
M VolgushevDepartment of Psychology, University of Connecticut, Storrs, CT 06269, USA. Electronic address: maxim.volgushev@uconn.edu.
University of Connecticut · US

Funding

The role of heterosynaptic plasticity in achieving stable yet adaptable memory stR01MH087631 · NIMH · UNIVERSITY OF CONNECTICUT STORRS · PI VOLGUSHEV, MAXIM · 2010 to 2014
$1.9M
NIMH NIH HHS R01 MH087631NIMH NIH HHS R01MH087631
6 · The paper itself

Abstract

Adenosine is a wide-spread endogenous neuromodulator. In the central nervous system it activates A1 and A2A receptors (A1Rs and A2ARs) which have differential distributions, different affinities to adenosine, are coupled to different G-proteins, and have opposite effects on synaptic transmission. Although effects of adenosine are studied in detail in several brain areas, such as the hippocampus and striatum, the heterogeneity of the effects of A1R and A2AR activation and their differential distribution preclude generalization over brain areas and cell types. Here we study adenosine's effects on excitatory synaptic transmission to layer 2/3 pyramidal neurons in slices of the rat visual cortex. We measured effects of bath application of adenosine receptor ligands on evoked excitatory postsynaptic potentials (EPSPs), miniature excitatory postsynaptic potentials (mEPSPs), and membrane properties. Adenosine reduced the amplitude of evoked EPSPs and excitatory postsynaptic currents (EPSCs), and reduced frequency of mEPSPs in a concentration-dependent and reversible manner. Concurrent with EPSP/C amplitude reduction was an increase in the paired-pulse ratio. These effects were blocked by application of the selective A1R antagonist DPCPX (8-cyclopentyl-1,3-dipropylxanthine), suggesting that activation of presynaptic A1Rs suppresses excitatory transmission by reducing release probability. Adenosine (20μM) hyperpolarized the cell membrane from -65.3±1.5 to -67.7±1.8mV, and reduced input resistance from 396.5±44.4 to 314.0±36.3MOhm (∼20%). These effects were also abolished by DPCPX, suggesting postsynaptic A1Rs. Application of the selective A2AR antagonist SCH-58261 (2-(2-furanyl)-7-(2-phenylethyl)-7H-pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidin-5-a-mine) on the background of high adenosine concentrations revealed an additional decrease in EPSP amplitude. Moreover, application of the A2AR agonist CGS-21680 (4-[2-[[6-amino-9-(N-ethyl-β-d-ribofuranuronamidosyl)-9H-purin-2-yl]amino]ethyl]benzenepropanoic acid hydrochloride) led to an A1R-dependent increase in mEPSP frequency. Dependence of the A2AR effects on the A1R availability suggests interaction between these receptors, whereby A2ARs exert their facilitatory effect on synaptic transmission by inhibiting the A1R-mediated suppression. Our results demonstrate functional pre and postsynaptic A1Rs and presynaptic A2ARs in layer 2/3 of the visual cortex, and suggest interaction between presynaptic A2ARs and A1Rs.

Indexed as

AdenosineAnimalsExcitatory Postsynaptic PotentialsIn Vitro TechniquesPyramidal CellsRatsRats, WistarSynaptic TransmissionVisual CortexAdenosine2-(2-furanyl)-7-(2-phenylethyl)-7H-pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidin-5-a-mine (A(2A)R antagonist)4-[2-[[6-amino-9-(N-ethyl-β-d-ribofuranuronamidosyl)-9H-purin-2-yl]amino]ethyl]benzenepropanoic acid hydrochloride (A(2A)R agonist)8-cyclopentyl-1,3-dipropylxanthine (A(1)R antagonist)A(1) and A(2A) receptorsA(1)RA(2A)Radenosineadenosine receptor type 1adenosine receptor type 2Aadenosine triphosphateAdoAPVATPCGS-21680d-(−)-2-amino-5-phosphonopentanoic acidDPCPXEPSCEPSPexcitatory postsynaptic currentexcitatory postsynaptic potentialmEPSPminiature excitatory postsynaptic potentialmodulationneocortexpresynapticSCH-58261synaptic transmissiontetrodotoxinTTX

Identifiers

PMID24355495
PMCPMC3960601
OpenAlexW1984835124

What OpenQuestion holds

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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.