Evidence map›Paper›PMID 27281752›Full record

ArticleJournal of neurophysiology2016

Two classes of excitatory synaptic responses in rat thalamic reticular neurons.

Charlotte Deleuze, John R Huguenard

Open access · bronzeAbstract read
In one paragraph

Article in Journal of neurophysiology, 2016. 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
2.0field-weighted citation impact, top 15% 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, 33 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
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  7. NMDA Receptors in the Lateral Preoptic Hypothalamus Are Essential for Sustaining NREM and REM Sleep.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  8. NaNeurobiology of disease · 2022
    Article
  9. Review
  10. Article
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  12. Article
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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.

Charlotte DeleuzeDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, California.
John R HuguenardDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, California John.Huguenard@stanford.edu.
Stanford University · US

Funding

Inhibitory Controls of Thalamic NeuronsR01NS034774 · NINDS · STANFORD UNIVERSITY · PI HUGUENARD, JOHN R · 1996 to 2021
$5.5M
Astrocytic Control of GABA Inhibition in EpilepsyR01NS090911 · NINDS · STANFORD UNIVERSITY · PI HUGUENARD, JOHN R · 2014 to 2017
$1.5M
Solid-state patch clamp platform to diagnose autism and screen for effective drugR21MH100717 · NIMH · STANFORD UNIVERSITY · PI HUGUENARD, JOHN R · 2013 to 2014
$427k
NIMH NIH HHS R21 MH100717NINDS NIH HHS R01 NS034774NINDS NIH HHS R01 NS090911
6 · The paper itself

Abstract

The thalamic reticular nucleus (nRt), composed of GABAergic cells providing inhibition of relay neurons in the dorsal thalamus, receives excitation from the neocortex and thalamus. The two excitatory pathways promoting feedback or feedforward inhibition of thalamocortical neurons contribute to sensory processing and rhythm generation. While synaptic inhibition within the nRt has been carefully characterized, little is known regarding the biophysics of synaptic excitation. To characterize the functional properties of thalamocortical and corticothalamic connections to the nRt, we recorded minimal electrically evoked excitatory postsynaptic currents from nRt cells in vitro. A hierarchical clustering algorithm distinguished two types of events. Type 1 events had larger amplitudes and faster kinetics, largely mediated by α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors, whereas type 2 responses had more prominent N-methyl-d-aspartate (NMDA) receptor contribution. Type 1 responses showed subnormal axonal propagation and paired pulse depression, consistent with thalamocortical inputs. Furthermore, responses kinetically similar to type 1 events were evoked by glutamate-mediated activation of thalamic neurons. Type 2 responses, in contrast, likely arise from corticothalamic inputs, with larger NMDA conductance and weak Mg(2+)-dependent block, suggesting that NMDA receptors are critical for the cortical excitation of reticular neurons. The long-lasting action of NMDA receptors would promote reticular cell burst firing and produce powerful inhibitory output to relay neurons proposed to be important in triggering epilepsy. This work provides the first complete voltage-clamp analysis of the kinetics and voltage dependence of AMPA and NMDA responses of thalamocortical and corticothalamic synapses in the nRt and will be critical in optimizing biologically realistic neural network models of thalamocortical circuits relevant to sensory processing and thalamocortical oscillations.

Indexed as

Analysis of VarianceAnimalsAnimals, NewbornBiophysicsCluster AnalysisElectric StimulationExcitatory Amino Acid AgentsExcitatory Postsynaptic PotentialsGlutamic AcidIn Vitro TechniquesNeuronsPatch-Clamp TechniquesRatsRats, Sprague-DawleySynapsesThalamic NucleiExcitatory Amino Acid AgentsGlutamic AcidcorticothalamicN-methyl-d-aspartate receptorthalamic reticular nucleusthalamocorticalα-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor

Identifiers

PMID27281752
PMCPMC5009213
OpenAlexW2409734885

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.