Evidence map›Paper›PMID 23100131›Full record

ArticleJournal of neurophysiology2013

Regulation of AMPA and NMDA receptor-mediated EPSPs in dendritic trees of thalamocortical cells.

Francis Lajeunesse, Helmut Kröger, Igor Timofeev

Open access · greenAbstract read
In one paragraph

Article in Journal of neurophysiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 51% 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

4 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Passive Synaptic Normalization and Input Synchrony-Dependent Amplification of Cortical Feedback in Thalamocortical Neuron Dendrites.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Article
  3. The Global Spike: Conserved Dendritic Properties Enable Unique Ca2+ Spike Generation in Low-Threshold Spiking Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  4. 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.

Francis LajeunesseCentre de recherche de l'Institut universitaire en santé mentale de Québec, Laval University, Québec, Canada.
Helmut Kröger
Igor Timofeev
Université Laval · CA

Funding

Cortical mechanisms and functional role of slow sleep oscillationsR01NS060870 · NINDS · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI BAZHENOV, MAKSIM V · 2008 to 2011
$1.3M
Canadian Institutes of Health Research MOP-37862Canadian Institutes of Health Research MOP-67175NINDS NIH HHS 1R01NS060870
6 · The paper itself

Abstract

Two main excitatory synapses are formed at the dendritic arbor of first-order nuclei thalamocortical (TC) neurons. Ascending sensory axons primarily establish contacts at large proximal dendrites, whereas descending corticothalamic fibers form synapses on thin distal dendrites. With the use of a multicomparment computational model based on fully reconstructed TC neurons from the ventroposterolateral nucleus of the cat, we compared local responses at the site of stimulation as well as somatic responses induced by both α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor (AMPAR)- and N-methyl-D-aspartate receptor (NMDAR)-mediated currents. We found that AMPAR-mediated responses, when synapses were located at proximal dendrites, induced a larger depolarization at the level of soma, whereas NMDAR-mediated responses were more efficient for synapses located at distal dendrites. The voltage transfer and transfer impedance were higher for NMDAR than for AMPAR activation at any location. For both types of synaptic current and for both input locations at the dendritic arbor, somatic responses were characterized by a low variability despite the large variability found in local responses in dendrites. The large neurons had overall smaller somatic responses than small neurons, but this relation was not found in local dendritic responses. We conclude that in TC cells, the dendritic location of small synaptic inputs does not play a major role in the amplitude of a somatic response, but the size of the neuron does. The variability of response amplitude between cells was much larger than the variability within cells. This suggests possible functional segregation of TC neurons of different size.

Indexed as

AnimalsCatsCerebral CortexDendritesExcitatory Postsynaptic PotentialsMembrane PotentialsModels, NeurologicalNeural PathwaysNeuronsReceptors, AMPAReceptors, N-Methyl-D-AspartateSynapsesSynaptic TransmissionThalamusReceptors, AMPAReceptors, N-Methyl-D-Aspartate

Identifiers

PMID23100131
PMCPMC3545156
OpenAlexW2010222533

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.