Evidence map›Paper›PMID 30506279›Full record

ArticleBrain structure & function2019

A specific olfactory cortico-thalamic pathway contributing to sampling performance during odor reversal learning.

Emmanuelle Courtiol, Michelle Neiman, Gloria Fleming, Catia M Teixeira, Donald A Wilson

Abstract read
In one paragraph

Article in Brain structure & function, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. 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

5 authors.

Emmanuelle CourtiolEmotional Brain Institute, Nathan Kline Institute for Psychiatric Research, 140 Old Orangeburg Road, Orangeburg, NY, 10962, USA. Emmanuelle.courtiol@cnrs.fr.ORCID http://orcid.org/0000-0002-7197-1117
Michelle NeimanEmotional Brain Institute, Nathan Kline Institute for Psychiatric Research, 140 Old Orangeburg Road, Orangeburg, NY, 10962, USA.
Gloria FlemingEmotional Brain Institute, Nathan Kline Institute for Psychiatric Research, 140 Old Orangeburg Road, Orangeburg, NY, 10962, USA.
Catia M TeixeiraEmotional Brain Institute, Nathan Kline Institute for Psychiatric Research, 140 Old Orangeburg Road, Orangeburg, NY, 10962, USA.
Donald A WilsonEmotional Brain Institute, Nathan Kline Institute for Psychiatric Research, 140 Old Orangeburg Road, Orangeburg, NY, 10962, USA.

Funding

CORTICAL PROCESSING OF OLFACTORY STIMULIR01DC003906 · NIDCD · UNIVERSITY OF OKLAHOMA NORMAN · PI WILSON, DONALD A · 1999 to 2017
$4.2M
Olfactory thalamus and odor perceptionR03DC014540 · NIDCD · NATHAN S. KLINE INSTITUTE FOR PSYCH RES · PI COURTIOL, EMMANUELLE · 2015 to 2017
$485k
National Institute on Deafness and Other Communication Disorders R01DC003906National Institute on Deafness and Other Communication Disorders R03DC014540NIDCD NIH HHS R01 DC003906NIDCD NIH HHS R03 DC014540
6 · The paper itself

Abstract

A growing body of evidence shows that olfactory information is processed within a thalamic nucleus in both rodents and humans. The mediodorsal thalamic nucleus (MDT) receives projections from olfactory cortical areas including the piriform cortex (PCX) and is interconnected with the orbitofrontal cortex (OFC). Using electrophysiology in freely moving rats, we recently demonstrated the representation of olfactory information in the MDT and the dynamics of functional connectivity between the PCX, MDT and OFC. Notably, PCX-MDT coupling is specifically increased during odor sampling of an odor discrimination task. However, whether this increase of coupling is functionally relevant is unknown. To decipher the importance of PCX-MDT coupling during the sampling period, we used optogenetics to specifically inactivate the PCX inputs to MDT during an odor discrimination task and its reversal in rats. We demonstrate that inactivating the PCX inputs to MDT does not affect the performance accuracy of an odor discrimination task and its reversal, however, it does impact the rats' sampling duration. Indeed, rats in which PCX inputs to MDT were inactivated during the sampling period display longer sampling duration during the odor reversal learning compared to controls-an effect not observed when inactivating OFC inputs to MDT. We demonstrate a causal link between the PCX inputs to MDT and the odor sampling performance, highlighting the importance of this specific cortico-thalamic pathway in olfaction.

Indexed as

OdorantsAnimalsDiscrimination LearningMaleOlfactory CortexOlfactory PathwaysOlfactory PerceptionRatsRats, Long-EvansReversal LearningThalamusMediodorsal thalamusOlfactionOrbitofrontal cortexPiriform cortexSampling

Identifiers

PMID30506279
PMCPMC6420857

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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.