Evidence map›Paper›PMID 33139568›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Differential attentional control mechanisms by two distinct noradrenergic coeruleo-frontal cortical pathways.

Andrea Bari, Sangyu Xu, Michele Pignatelli, Daigo Takeuchi, Jiesi Feng, Yulong Li, Susumu Tonegawa

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

59 citing papers in PubMed, 113 citations in OpenAlex.

  1. Article
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  4. Galanin receptor 1 expressing neurons in hippocampal-prefrontal circuitry modulate goal directed attention and impulse control.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  5. Article
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  7. Visual attention is linked to temporally structured noradrenaline release in the medial prefrontal cortex.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 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

7 authors at 2 institutions in 2 countries.

Andrea BariRIKEN-MIT Laboratory for Neural Circuit Genetics, Picower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, MA 02139; baria@mit.edu tonegawa@mit.edu.
Sangyu XuRIKEN-MIT Laboratory for Neural Circuit Genetics, Picower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, MA 02139.
Michele PignatelliRIKEN-MIT Laboratory for Neural Circuit Genetics, Picower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, MA 02139.ORCID 0000-0002-4918-2066
Daigo TakeuchiRIKEN-MIT Laboratory for Neural Circuit Genetics, Picower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, MA 02139.
Jiesi FengState Key Laboratory of Membrane Biology, Peking University School of Life Sciences, 100871 Beijing, China.ORCID 0000-0003-3635-2625
Yulong LiState Key Laboratory of Membrane Biology, Peking University School of Life Sciences, 100871 Beijing, China.ORCID 0000-0002-9166-9919
Susumu TonegawaRIKEN-MIT Laboratory for Neural Circuit Genetics, Picower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, MA 02139; baria@mit.edu tonegawa@mit.edu.ORCID 0000-0003-2839-8228
Massachusetts Institute of Technology · USPeking University · CN

Funding

Novel fluorescent sensors based on GPCRs for imaging neuromodulationU01NS103558 · NINDS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI HIRES, SAMUEL ANDREW, LI, YULONG · 2017 to 2019
$2.2M
NINDS NIH HHS U01 NS103558
6 · The paper itself

Abstract

The attentional control of behavior is a higher-order cognitive function that operates through attention and response inhibition. The locus coeruleus (LC), the main source of norepinephrine in the brain, is considered to be involved in attentional control by modulating the neuronal activity of the prefrontal cortex (PFC). However, evidence for the causal role of LC activity in attentional control remains elusive. Here, by using behavioral and optogenetic techniques, we investigate the effect of LC neuron activation or inhibition in operant tests measuring attention and response inhibition (i.e., a measure of impulsive behavior). We show that LC neuron stimulation increases goal-directed attention and decreases impulsivity, while its suppression exacerbates distractibility and increases impulsive responding. Remarkably, we found that attention and response inhibition are under the control of two divergent projections emanating from the LC: one to the dorso-medial PFC and the other to the ventro-lateral orbitofrontal cortex, respectively. These findings are especially relevant for those pathological conditions characterized by attention deficits and elevated impulsivity.

Indexed as

AnimalsAttentionBrainCognitionFrontal LobeImpulsive BehaviorInhibition, PsychologicalLocus CoeruleusMiceMice, TransgenicNeuronsNorepinephrinePrefrontal CortexNorepinephrineattentional controllocus coeruleusnorepinephrineprefrontal cortexresponse inhibition

Identifiers

PMID33139568
PMCPMC7682591
OpenAlexW3096841042

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.