Evidence map›Paper›PMID 34783016›Full record

ArticleThe Journal of physiology2021

Corticothalamic projections deliver enhanced responses to medial geniculate body as a function of the temporal reliability of the stimulus.

Srinivasa P Kommajosyula, Edward L Bartlett, Rui Cai, Lynne Ling, Donald M Caspary

Abstract read
In one paragraph

Article in The Journal of physiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Timing and Convergence of Ensemble Activity Govern Auditory Thalamocortical Transmission.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
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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

5 authors.

Srinivasa P KommajosyulaDepartment of Pharmacology, Southern Illinois University School of Medicine, Springfield, IL, USA.ORCID 0000-0003-3467-6896
Edward L BartlettDepartment of Biological Sciences and the Weldon School of Biomedical Engineering, Purdue University, West Lafayette, IN, USA.
Rui CaiDepartment of Pharmacology, Southern Illinois University School of Medicine, Springfield, IL, USA.
Lynne LingDepartment of Pharmacology, Southern Illinois University School of Medicine, Springfield, IL, USA.
Donald M CasparyDepartment of Pharmacology, Southern Illinois University School of Medicine, Springfield, IL, USA.ORCID 0000-0001-5993-6004

Funding

CODING IN AUDITORY NEURONS: EFFECTS OF AMINO ACIDSR01DC000151 · NIDCD · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI CASPARY, DONALD M. · 1989 to 2024
$7.1M
Coding in Auditory Neurons: Effects of Amino AcidsR56DC000151 · NIDCD · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI CASPARY, DONALD M. · 2010 to 2010
$128k
MINORITY PREDOCTORAL FELLOWSHIP PROGRAM - NIGMSF31DC000151 · NIDCD · CORNELL UNIVERSITY ITHACA · PI HERMER-VAZQUEZ, RAYMOND W · 1993 to 1995
–
NIDCD NIH HHS DC000151NIDCD NIH HHS F31 DC000151NIDCD NIH HHS R01 DC000151NIDCD NIH HHS R56 DC000151
6 · The paper itself

Abstract

Ageing and challenging signal-in-noise conditions are known to engage the use of cortical resources to help maintain speech understanding. Extensive corticothalamic projections are thought to provide attentional, mnemonic and cognitive-related inputs in support of sensory inferior colliculus (IC) inputs to the medial geniculate body (MGB). Here we show that a decrease in modulation depth, a temporally less distinct periodic acoustic signal, leads to a jittered ascending temporal code, changing MGB unit responses from adapting responses to responses showing repetition enhancement, posited to aid identification of important communication and environmental sounds. Young-adult male Fischer Brown Norway rats, injected with the inhibitory opsin archaerhodopsin T (ArchT) into the primary auditory cortex (A1), were subsequently studied using optetrodes to record single-units in MGB. Decreasing the modulation depth of acoustic stimuli significantly increased repetition enhancement. Repetition enhancement was blocked by optical inactivation of corticothalamic terminals in MGB. These data support a role for corticothalamic projections in repetition enhancement, implying that predictive anticipation could be used to improve neural representation of weakly modulated sounds. KEY POINTS: In response to a less temporally distinct repeating sound with low modulation depth, medial geniculate body (MGB) single units show a switch from adaptation towards repetition enhancement. Repetition enhancement was reversed by blockade of MGB inputs from the auditory cortex. Collectively, these data argue that diminished acoustic temporal cues such as weak modulation engage cortical processes to enhance coding of those cues in auditory thalamus.

Indexed as

Auditory CortexGeniculate BodiesAcoustic StimulationAnimalsMaleNeuronsRatsReproducibility of Resultsauditory thalamusless distinct modulated stimulirepetition enhancementsensory adaptation

Identifiers

PMID34783016
PMCPMC10630908

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Registered trials

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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.