Evidence map›Paper›PMID 10766918›Full record

ArticleThe Journal of physiology2000

Enhancement of NMDA receptor-mediated currents by light in rat neurones in vitro.

D N Leszkiewicz, K Kandler, E Aizenman

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.9field-weighted citation impact, top 32% 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

17 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Discovery of GluN2A subtype-selectiveActa pharmaceutica Sinica. B · 2024
    Review
  3. Article
  4. Review
  5. Review
  6. Mapping Auditory Synaptic Circuits with Photostimulation of Caged Glutamate.Methods in molecular biology (Clifton, N.J.) · 2016
    Article
  7. Encephalopsin (OPN3) protein abundance in the adult mouse brain.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2012
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. p38 activation is required upstream of potassium current enhancement and caspase cleavage in thiol oxidant-induced neuronal apoptosis.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2001
    Article
  15. Functional redundancy of cryptochromes and classical photoreceptors for nonvisual ocular photoreception in mice.Proceedings of the National Academy of Sciences of the United States of America · 2000
    Article
  16. Article
  17. 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

3 authors at 1 institution in 1 country.

D N LeszkiewiczDepartment of Neurobiology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.
K Kandler
E Aizenman
University of Pittsburgh · US

Funding

Development of Neuronal Circuits In The Auditory SystemsR01DC004199 · NIDCD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KANDLER, KARL · 1999 to 2020
$8.5M
REDOX MODULATION OF NMDA RECEPTORSR01NS029365 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI AIZENMAN, ELIAS · 1991 to 2003
$1.2M
NIDCD NIH HHS DC04199NIDCD NIH HHS R01 DC004199NINDS NIH HHS NS29365
6 · The paper itself

Abstract

1. N-Methyl-D-aspartate (NMDA) receptor function can be modified by the action of several endogenous and exogenous modulatory processes. In the present study, we report that brief pulses of light potentiate NMDA, but not non-NMDA glutamatergic receptor-mediated whole-cell and single channel currents in rat cortical neurones in vitro. In addition, light also potentiated NMDA receptor-mediated whole-cell responses in isolated rat retinal neurones. 2. Potentiation of NMDA whole-cell currents in cortical neurones was readily observed during and following a brief (< 2 s) exposure of neurones to wavelengths of less than 324 nm of relatively bright light (0.09 microW microm-2). In addition, prolonged exposures (> 30 s) to visible wavelengths (> 380 nm) or to attenuated light (1-3 % transmittance of non-attenuated light) were also sufficient to enhance NMDA receptor-mediated responses. 3. The light-induced potentiation of NMDA receptor-mediated currents persisted for several minutes, slowly reversing to control levels with a time constant of approximately 5 min. A subsequent exposure to light could potentiate NMDA receptor-mediated currents for a second time. 4. Light did not alter the apparent affinity of the NMDA receptor for the co-agonists NMDA and glycine. Additionally, potentiation of the NMDA-induced currents was not mediated by a change in the pH sensitivity of the receptor. In excised outside-out membrane patches, the effects of light on NMDA-activated unitary currents were manifested as a twofold increase in channel open frequency without alterations in single channel amplitude or open time. 5. Our results suggest the presence of a light-sensitive moiety within the NMDA receptor, or in a closely associated structure, which affects channel properties. This previously unrecognized form of NMDA receptor modulation may provide a tool for understanding the conformational changes associated with its gating. In addition, it is possible that light may affect NMDA receptor-mediated function or dysfunction in the retina.

Indexed as

AnimalsElectric StimulationElectrophysiologyIn Vitro TechniquesMembrane PotentialsNeuronsN-MethylaspartatePatch-Clamp TechniquesPhotic StimulationProtonsRatsRats, Sprague-DawleyReceptors, GlycineReceptors, N-Methyl-D-AspartateN-MethylaspartateProtonsReceptors, GlycineReceptors, N-Methyl-D-Aspartate

Identifiers

PMID10766918
PMCPMC2269867
OpenAlexW2009965529

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.