Evidence map›Paper›PMID 39151432›Full record

ArticleCurrent biology : CB2024

Strategic stabilization of arousal boosts sustained attention.

Jan Willem de Gee, Zakir Mridha, Marisa Hudson, Yanchen Shi, Hannah Ramsaywak, Spencer Smith, Nishad Karediya, Matthew Thompson, Kit Jaspe, Hong Jiang and 2 more

Abstract read
In one paragraph

Article in Current biology : CB, 2024. 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. Neural and autonomic predictors of future listening errors.bioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Benefits of Dual-Tasking on Implicit Sensorimotor Adaptation.The European journal of neuroscience · 2026
    Article
  7. Article
  8. Article
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

12 authors.

Jan Willem de GeeDepartment of Neuroscience, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, 1250 Moursund Street, Houston, TX 77030, USA; Cognitive and Systems Neuroscience, Swammerdam Institute for Life Sciences, University of Amsterdam, Science Park 904, Amsterdam 1098 XH, the Netherlands; Research Priority Area Brain and Cognition, University of Amsterdam, Science Park 904, Amsterdam 1098 XH, the Netherlands. Electronic address: j.w.degee@uva.nl.
Zakir MridhaDepartment of Neuroscience, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, 1250 Moursund Street, Houston, TX 77030, USA.
Marisa HudsonDepartment of Neuroscience, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, 1250 Moursund Street, Houston, TX 77030, USA.
Yanchen ShiDepartment of Neuroscience, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, 1250 Moursund Street, Houston, TX 77030, USA.
Hannah RamsaywakDepartment of Neuroscience, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, 1250 Moursund Street, Houston, TX 77030, USA.
Spencer SmithDepartment of Neuroscience, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, 1250 Moursund Street, Houston, TX 77030, USA.
Nishad KarediyaDepartment of Neuroscience, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, 1250 Moursund Street, Houston, TX 77030, USA.
Matthew ThompsonDepartment of Neuroscience, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, 1250 Moursund Street, Houston, TX 77030, USA.
Kit JaspeDepartment of Neuroscience, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, 1250 Moursund Street, Houston, TX 77030, USA.
Hong JiangDepartment of Neuroscience, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, 1250 Moursund Street, Houston, TX 77030, USA.
Wenhao ZhangDepartment of Neuroscience, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, 1250 Moursund Street, Houston, TX 77030, USA.
Matthew J McGinleyDepartment of Neuroscience, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, 1250 Moursund Street, Houston, TX 77030, USA; Department of Electrical and Computer Engineering, Rice University, 6100 Main Street, Houston, TX 77005, USA. Electronic address: matthew.mcginley@bcm.edu.

Funding

Elucidating neural circuits and pupil readouts of motivated effortful listeningR01DC017797 · NIDCD · BAYLOR COLLEGE OF MEDICINE · PI MCGINLEY, MATTHEW J · 2019 to 2023
$2.4M
Neuromodulatory mechanisms of listening effortR03DC015618 · NIDCD · BAYLOR COLLEGE OF MEDICINE · PI MCGINLEY, MATTHEW J · 2016 to 2018
$476k
NIDCD NIH HHS R01 DC017797NIDCD NIH HHS R03 DC015618
6 · The paper itself

Abstract

Arousal and motivation interact to profoundly influence behavior. For example, experience tells us that we have some capacity to control our arousal when appropriately motivated, such as staying awake while driving a motor vehicle. However, little is known about how arousal and motivation jointly influence decision computations, including if and how animals, such as rodents, adapt their arousal state to their needs. Here, we developed and show results from an auditory, feature-based, sustained-attention task with intermittently shifting task utility. We use pupil size to estimate arousal across a wide range of states and apply tailored signal-detection theoretic, hazard function, and accumulation-to-bound modeling approaches in a large cohort of mice. We find that pupil-linked arousal and task utility both have major impacts on multiple aspects of task performance. Although substantial arousal fluctuations persist across utility conditions, mice partially stabilize their arousal near an intermediate and optimal level when task utility is high. Behavioral analyses show that multiple elements of behavior improve during high task utility and that arousal influences some, but not all, of them. Specifically, arousal influences the likelihood and timescale of sensory evidence accumulation but not the quantity of evidence accumulated per time step while attending. In sum, the results establish specific decision-computational signatures of arousal, motivation, and their interaction in attention. So doing, we provide an experimental and analysis framework for studying arousal self-regulation in neurotypical brains and in diseases such as attention-deficit/hyperactivity disorder.

Indexed as

ArousalAttentionAnimalsDecision MakingFemaleMaleMiceMice, Inbred C57BLMotivationPupilarousalattentionevidence accumulationlistening effortmotivationpupilsensitivitysignal detection theorysurvival analysistask utility

Identifiers

PMID39151432
PMCPMC11447271

What OpenQuestion holds

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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.