Evidence map›Paper›PMID 8795623›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience1996

Enhanced fast synaptic transmission and a delayed depolarization induced by transient potassium current blockade in rat hippocampal slice as studied by optical recording.

M E Barish, M Ichikawa, T Tominaga, G Matsumoto, T Iijima

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

16 citing papers in PubMed, 47 citations in OpenAlex.

  1. Downmodulation of Potassium Conductances Induces Epileptic Seizures in Cortical Network Models Via Multiple Synergistic Factors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  2. Assessing seizure liabilityFrontiers in cellular neuroscience · 2023
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  10. Imaging spatio-temporal patterns of long-term potentiation in mouse hippocampus.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2003
    Article
  11. Article
  12. Article
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  14. Optical detection of synaptically induced glutamate transport in hippocampal slices.The Journal of neuroscience : the official journal of the Society for Neuroscience · 1999
    Article
  15. Changes in mitochondrial function resulting from synaptic activity in the rat hippocampal slice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 1998
    Article
  16. 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

5 authors at 1 institution in 2 countries.

M E BarishSection of Cellular and Molecular Neuroscience, Electrotechnical Laboratory, Ibaraki, Japan.
M Ichikawa
T Tominaga
G Matsumoto
T Iijima
Laboratory of Molecular Genetics · PL

Funding

DIFFERENTIATION OF NEURONAL SIGNALING MECHANISMSR01NS023857 · NINDS · UNIVERSITY OF CALIFORNIA IRVINE · PI BARISH, MICHAEL E · 1986 to 2000
$253k
INTRACELLULAR CALCIUM IN HIPPOCAMPAL NEURONSR01NS034581 · NINDS · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI BARISH, MICHAEL E · 1995 to 1997
–
NINDS NIH HHS NS23857NINDS NIH HHS NS34581
6 · The paper itself

Abstract

In hippocampal neurons, a slowly inactivating aminopyridine-sensitive transient potassium current, D-current, influences the time course of action potential repolarization and therefore activity-dependent Ca2+ entry. We used high-speed optical recording techniques to study the effects of selectively inhibiting D-current with 4-AP (40 microM) on transmission at the Schaffer collateral (CA3)-CA1 synapse in rat hippocampal slices stained with the voltage-sensitive dye RH-155. We observed that addition of 4-AP to the bathing solution resulted in (1) augmentation of a fast component of the optical signal corresponding to the postsynaptic EPSP and action potential, and (2) the appearance of a delayed depolarization of CA1 neurons and other adjacent cells. 4-AP appeared to alter the presynaptic action potential and the dynamics of synaptic transmission to both reduce the sensitivity of the postsynaptic EPSP and action potential to omega-toxin calcium channel blockers (omega-conotoxin GVIA and omega-agatoxin IVA) and the Ca(2+)-dependent potassium channel blocker charybdotoxin, and to increase sensitivity to the dihydropyridine nifedipine, the NMDA receptor blocker aminophosphonopentanoic acid, and the intracellular Ca2+ release inhibitor thapsigargin. The delayed depolarization induced by 4-AP was inhibited in hyperosmotic extracellular solution, suggesting that enhanced transmitter release resulted in increased accumulation of K+ in the extracellular space. Because 4-AP is a convulsant at concentrations similar to those used here, we suggest that the 4-AP-targeted channel(s) carrying D-current may contribute to the hyperexcitability associated with epilepsy.

Indexed as

4-AminopyridineAnimalsBicucullineElectrophysiologyGABA Antagonistsgamma-Aminobutyric AcidGlutamineHippocampusIn Vitro TechniquesMaleMicroelectrodesOptics and PhotonicsPotassiumPresynaptic TerminalsRatsSignal Transduction4-AminopyridineBicucullineGABA Antagonistsgamma-Aminobutyric AcidGlutaminePotassium

Identifiers

PMID8795623
PMCPMC6578979
OpenAlexW2156138790

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.