Evidence map›Paper›PMID 11508493›Full record

ArticleNeuroscience and behavioral physiology

NMDA glutamate receptor antagonists selectively affect the synaptic mechanisms of nociceptive sensitization in snails.

V P Nikitin, S A Kozyrev, A V Shevelkin

Abstract read
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Article in Neuroscience and behavioral physiology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 2 institutions in 2 countries.

V P NikitinP. K. Anokhin Science Research Institute of Normal Physiology, Russian Academy of Medical Sciences, Moscow.
S A Kozyrev
A V Shevelkin
Institute of Normal Physiology named after P.K. Anokhin · RUAcademy of Medical Sciences · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Defensive behavior command neurons LP11 and RP11 were studied in semi-intact snail preparations to investigate the effects of N-methyl-D-aspartate (NMDA) receptor antagonists on the mechanisms of nociceptive sensitization. Application of sensitizing stimuli to the heads of control snails led to membrane depolarization and increased excitability, and also depressed the responses of neurons to tactile and chemical sensory stimuli in the short-term stage and facilitated responses in the long-term stage of sensitization. Development of sensitization in conditions of exposure to the NMDA receptor antagonists AP5 or MK-801 produced changes in the membrane potential and membrane excitability of command neurons similar to those seen in neurons of control sensitized snails. In addition, changes in the responses of command neurons to tactile stimulation of the head and foot and chemical stimulation of the foot in these conditions were also similar to those seen in neurons of control animals. Acquisition of sensitization during administration of NMDA receptor antagonists led to pronounced depression of responses to chemical test sensory stimulation of the snails' heads in both the short-term and long-term stages of sensitization. Thus. in sensitized snails. NMDA glutamate receptor antagonists selectively acted on the mechanisms of induction of plasticity the synaptic "inputs" of command neurons mediating excitation from chemical sensory stimuli from the animal's head.

Indexed as

AnimalsCell MembraneElectric StimulationElectrophysiologyEvoked PotentialsExcitatory Amino Acid AntagonistsExcitatory Postsynaptic PotentialsHelix, SnailsMembrane PotentialsNeuronal PlasticityNeuronsNociceptorsPhysical StimulationReceptors, N-Methyl-D-AspartateStimulation, ChemicalSynapsesExcitatory Amino Acid AntagonistsReceptors, N-Methyl-D-Aspartate

Identifiers

PMID11508493
OpenAlexW207615336

What OpenQuestion holds

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Read underepoch 390

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.