Evidence map›Paper›PMID 10066246›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience1999

Temperature-dependent modulation of excitatory transmission in hippocampal slices is mediated by extracellular adenosine.

S A Masino, T V Dunwiddie

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.8field-weighted citation impact, top 5% 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

34 citing papers in PubMed, 102 citations in OpenAlex.

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  9. Many parameter sets in a multicompartment model oscillator are robust to temperature perturbations.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
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  16. Purinergic mechanisms in gliovascular coupling.Seminars in cell & developmental biology · 2011
    Review
  17. Calcium-independent inhibitory G-protein signaling induces persistent presynaptic muting of hippocampal synapses.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2011
    Article
  18. Article
  19. Metabolic autocrine regulation of neurons involves cooperation among pannexin hemichannels, adenosine receptors, and KATP channels.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2010
    Article
  20. Control of cannabinoid CB1 receptor function on glutamate axon terminals by endogenous adenosine acting at A1 receptors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2010
    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

2 authors at 2 institutions in 1 country.

S A MasinoNeuroscience Program, University of Colorado Health Sciences Center, Denver, Colorado 80262, USA.
T V Dunwiddie
Society for Neuroscience · USUniversity of Colorado Health · US

Funding

ADENOSINE AND MODULATION OF SYNAPTIC TRANSMISSIONR01NS029173 · NINDS · UNIVERSITY OF COLORADO DENVER · PI MASINO, SUSAN A · 1991 to 2004
$1.2M
NINDS NIH HHS R01 NS029173NINDS NIH HHS R01 NS 29173
6 · The paper itself

Abstract

Although extracellular adenosine concentrations in brain are increased markedly by a variety of stimuli such as hypoxia and ischemia, it has been difficult to demonstrate large increases in adenosine with stimuli that do not result in pathological tissue damage. The present studies demonstrate that increasing the temperature at which rat hippocampal brain slices are maintained (typically from 32.5 to 38.5 degrees C) markedly inhibits excitatory synaptic transmission. This effect was reversible on cooling, readily repeatable, and was blocked by A1 receptor antagonists and by adenosine deaminase, suggesting that it was mediated by increased activation of presynaptic adenosine A1 receptors by endogenous adenosine. This increase in adenosinergic inhibition was not a response to hyperthermia per se, because it could be elicited by temperatures that remained entirely within the hypothermic range (e. g., from 32.5 to 35.5 degrees C). The increased activity at A1 receptors appeared to be attributable to the direct release of adenosine via nucleoside transporters; the release of adenine nucleotides, linked to either the activation of NMDA receptors or the increased efflux of cAMP, appeared not to be involved. These results suggest that changes in brain temperature can alter the regulation of extracellular adenosine in rat brain slices and that increased adenosine release may be an important regulatory mechanism for countering increased excitability consequent to increased brain temperature.

Indexed as

TemperatureAdenosineAnimalsExtracellular SpaceHippocampusIn Vitro TechniquesNeural InhibitionRatsRats, Sprague-DawleySynapsesSynaptic TransmissionAdenosine

Identifiers

PMID10066246
PMCPMC6782539
OpenAlexW2113792847

What OpenQuestion holds

Texttitle and abstract
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.