Evidence map›Paper›PMID 10694206›Full record

ArticleBritish journal of pharmacology2000

Sustained ethanol inhibition of native AMPA receptors on medial septum/diagonal band (MS/DB) neurons.

G D Frye, A Fincher

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.7field-weighted citation impact, top 38% 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, 34 citations in OpenAlex.

  1. Deleterious effects of a low amount of ethanol on LTP-like plasticity in human cortex.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2014
    Trial
  2. Synaptic Effects Induced by Alcohol.Current topics in behavioral neurosciences · 2025
    Review
  3. Article
  4. Article
  5. Role of GABAMolecular brain · 2017
    Review
  6. Review
  7. Synaptic effects induced by alcohol.Current topics in behavioral neurosciences · 2013
    Review
  8. Article
  9. Perturbation of the glutamate-glutamine system in alcohol dependence and remission.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2011
    Article
  10. Review
  11. Effects of topiramate and other anti-glutamatergic drugs on the acute intoxicating actions of ethanol in mice: modulation by genetic strain and stress.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2009
    Article
  12. Article
  13. Review
  14. Article
  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

2 authors at 1 institution in 1 country.

G D FryeDepartment of Medical Pharmacology and Toxicology, College of Medicine, Texas A&M Health Science Center, College Station, Texas, TX 77843-1114, USA. gdfrye@tamu.edu
A Fincher
Texas College · US

Funding

SYNAPTIC MECHANISMS OF ACUTE ETHANOL TOLERANCER01AA010067 · NIAAA · TEXAS ENGINEERING EXPERIMENT STATION · PI FRYE, GERALD D · 1995 to 1997
–
NIAAA NIH HHS AA10067
6 · The paper itself

Abstract

The direct impact of ethanol on native, non-NMDA glutamate receptors was examined in acutely isolated MS/DB neurons from rat. The impact of ethanol functional tolerance and physical dependence on non-NMDA receptor function was also determined. Non-NMDA receptors were defined pharmacologically as predominantly the AMPA subtype, because both AMPA- or kainate-activated currents were blocked by GYKI 52466, a selective AMPA receptor antagonist. The relative magnitude of potentiation of AMPA-activated currents by 10 or 100 microM cyclothiazide was consistent with recombinant AMPA flop-subtype receptors. Finally, the selective kainate receptor agonist, SYM 8021, induced little current in MS/DB neurons. AMPA receptor currents when activated by kainate were sensitive to ethanol, showing inhibition of approximately 5 - 50% when 10 - 300 mM ethanol and kainate were briefly co-applied (3 s). Ethanol (100 mM) also inhibited both the initial transient peak and sustained currents activated by AMPA. Inhibition was sustained during continuous ethanol superfusions of 5 min, suggesting a lack of acute tolerance to ethanol-induced AMPA receptor blockade. Rapid application of 3 - 3000 microM kainate activated concentration-dependent currents in MS/DB neurons from Control and Ethanol Dependent animals that were not significantly different. Also, direct ethanol inhibition (300 mM) of kainate-activated currents was not reduced by ethanol dependence, suggesting a lack of functional tolerance. These results suggest that native AMPA receptors on MS/DB neurons are inhibited by pharmacologically-relevant concentrations of ethanol. However, these receptors, unlike NMDA receptors, do not undergo adaptation with sustained ethanol exposure sufficient to induce physical dependence. British Journal of Pharmacology (2000) 129, 87 - 94

Indexed as

Benzodiazepinesalpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic AcidAnimalsAnti-Anxiety AgentsCentral Nervous System DepressantsDiagonal Band of BrocaEthanolExcitatory Amino Acid AgonistsExcitatory Amino Acid AntagonistsKainic AcidKainic Acid ReceptorsMaleNeuronal PlasticityNeuronsPatch-Clamp TechniquesRatsalpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic AcidAnti-Anxiety AgentsBenzodiazepinesCentral Nervous System DepressantsEthanolExcitatory Amino Acid AgonistsExcitatory Amino Acid AntagonistsGYKI 52466Kainic AcidKainic Acid ReceptorsReceptors, AMPAReceptors, N-Methyl-D-Aspartate

Identifiers

PMID10694206
PMCPMC1621129
OpenAlexW2021260503

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.