Evidence map›Paper›PMID 23615551›Full record

ArticleJournal of neurophysiology2013

Thalamic microcircuits: presynaptic dendrites form two feedforward inhibitory pathways in thalamus.

Shane R Crandall, Charles L Cox

Abstract 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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Article
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  8. Review
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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.

Shane R CrandallDepartment of Pharmacology, University of Illinois, Urbana, IL, USA.
Charles L Cox

Funding

Modulation of Subcortical Visual Information ProcessingR01EY014024 · NEI · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI COX, CHARLES LEROY · 2003 to 2012
$2.6M
Modulation of Subcortical Visual Information ProcessingR56EY014024 · NEI · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI COX, CHARLES LEROY · 2009 to 2009
$384k
Functions of naturally diverse inhibitory networks in neocortexF32NS084763 · NINDS · BROWN UNIVERSITY · PI CRANDALL, SHANE R · 2013 to 2015
$159k
NEI NIH HHS EY-014024NEI NIH HHS R01 EY014024NINDS NIH HHS F32 NS084763
6 · The paper itself

Abstract

In the visual thalamus, retinal afferents activate both local interneurons and excitatory thalamocortical relay neurons, leading to robust feedforward inhibition that regulates the transmission of sensory information from retina to neocortex. Peculiarly, this feedforward inhibitory pathway is dominated by presynaptic dendrites. Previous work has shown that the output of dendritic terminals of interneurons, also known as F2 terminals, are regulated by both ionotropic and metabotropic glutamate receptors. However, it is unclear whether both classes of glutamate receptors regulate output from the same or distinct dendritic terminals. Here, we used focal glutamate uncaging and whole cell recordings to reveal two types of F2 responses in rat visual thalamus. The first response, which we are calling a Type-A response, was mediated exclusively by ionotropic glutamate receptors (i.e., AMPA and NMDA). In contrast, the second response, which we are calling a Type-B response, was mediated by a combination of ionotropic and type 5 metabotropic glutamate receptors (i.e., mGluR(5)). In addition, we demonstrate that both F2 responses are evoked in the same postsynaptic neurons, which are morphologically distinct from neurons in which no F2 responses are observed. Since photostimulation was relatively focal and small in magnitude, these results suggest distinct F2 terminals, or small clusters of terminals, could be responsible for generating the two inhibitory responses observed. Because of the nature of ionotropic and metabotropic glutamate receptors, we predict the efficacy by which the retina communicates with the thalamus would be strongly regulated by 1) the activity level of a given retinogeniculate axon, and 2) the specific type of F2 terminals activated.

Indexed as

AnimalsDendritesFemaleGABAergic NeuronsGeniculate BodiesInterneuronsIn Vitro TechniquesMaleNeural InhibitionNeuronsPresynaptic TerminalsRatsReceptors, GlutamateReceptors, Glutamatedorsal lateral geniculate nucleusglutamate uncaginginterneuronpresynaptic dendritetwo-photon imaging

Identifiers

PMID23615551
PMCPMC3727071

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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.