Evidence map›Paper›PMID 37714750›Full record

ArticleBritish journal of anaesthesia2023

Early-in-life isoflurane exposure alters resting-state functional connectivity in juvenile non-human primates.

Viola Neudecker, Jose F Perez-Zoghbi, Oscar Miranda-Domínguez, Katie J Schenning, Julian Sb Ramirez, A J Mitchell, Anders Perrone, Eric Earl, Sam Carpenter, Lauren D Martin and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in British journal of anaesthesia, 2023. 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
1.6field-weighted citation impact, top 18% 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

8 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Social Housing of Postoperative Animals to Support Animal Welfare.Journal of the American Association for Laboratory Animal Science : JAALAS · 2026
    Review
  4. Article
  5. Article
  6. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 5 institutions in 1 country.

Viola NeudeckerDepartment of Anesthesiology, Columbia University Medical Center, New York, NY, USA.
Jose F Perez-ZoghbiDepartment of Anesthesiology, Columbia University Medical Center, New York, NY, USA.
Oscar Miranda-DomínguezClinical Behavioral Neuroscience Masonic Institute for the Developing Brain, Minneapolis, MN, USA.
Katie J SchenningDepartment of Anesthesiology and Perioperative Medicine, Oregon Health & Science University, Portland, OR, USA.
Julian Sb RamirezDepartment of Behavioral Neuroscience, Oregon Health & Science University, Portland, OR, USA.
A J MitchellDepartment of Behavioral Neuroscience, Oregon Health & Science University, Portland, OR, USA.
Anders PerroneClinical Behavioral Neuroscience Masonic Institute for the Developing Brain, Minneapolis, MN, USA.
Eric EarlData Science and Sharing Team, National Institute of Mental Health, Bethesda, MD, USA.
Sam CarpenterDepartment of Behavioral Neuroscience, Oregon Health & Science University, Portland, OR, USA.
Lauren D MartinAnimal Resources & Research Support, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR, USA.
Kristine ColemanDivision of Neuroscience, Oregon National Primate Research Center, Oregon Health & Science University, Portland, OR, USA.
Martha NeuringerDivision of Neuroscience, Oregon National Primate Research Center, Oregon Health & Science University, Portland, OR, USA.
Christopher D KroenkeDivision of Neuroscience, Oregon National Primate Research Center, Oregon Health & Science University, Portland, OR, USA; Advanced Imaging Research Center, Oregon Health & Science University, Portland, OR, USA.
Gregory A DissenDivision of Neuroscience, Oregon National Primate Research Center, Oregon Health & Science University, Portland, OR, USA.
Damien A FairClinical Behavioral Neuroscience Masonic Institute for the Developing Brain, Minneapolis, MN, USA.
Ansgar M BrambrinkDepartment of Anesthesiology, Columbia University Medical Center, New York, NY, USA. Electronic address: amb2457@cumc.columbia.edu.
Oregon National Primate Research Center · USOregon Health & Science University · USAllen Institute for Brain Science · USColumbia University Irving Medical Center · USNational Institute of Mental Health · US

Funding

Upgrade of confocal microscopy at the Oregon National Primate Research CenterP51OD011092 · OD · OREGON HEALTH & SCIENCE UNIVERSITY · PI Bonnie J. Nagel · 2012 to 2026
$203.9M
NEUROSCIENCE TRAINING IN DRUG ABUSE RESEARCHT32DA007234 · NIDA · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Paul G Mermelstein, Jocelyn M Richard · 1986 to 2026
$10.9M
NIDA NIH HHS T32 DA007234NIH HHS P51 OD011092
6 · The paper itself

Abstract

backgroundClinical studies suggest that anaesthesia exposure early in life affects neurobehavioural development. We designed a non-human primate (NHP) study to evaluate cognitive, behavioural, and brain functional and structural alterations after isoflurane exposure during infancy. These NHPs displayed decreased close social behaviour and increased astrogliosis in specific brain regions, most notably in the amygdala. Here we hypothesise that resting-state functional connectivity MRI can detect alterations in connectivity of brain areas that relate to these social behaviours and astrogliosis.

methodsImaging was performed in 2-yr-old NHPs under light anaesthesia, after early-in-life (postnatal days 6-12) exposure to 5 h of isoflurane either one or three times, or to room air. Brain images were segmented into 82 regions of interest; the amygdala and the posterior cingulate cortex were chosen for a seed-based resting-state functional connectivity MRI analysis.

resultsWe found differences between groups in resting-state functional connectivity of the amygdala and the auditory cortices, medial premotor cortex, and posterior cingulate cortex. There were also alterations in resting-state functional connectivity between the posterior cingulate cortex and secondary auditory, polar prefrontal, and temporal cortices, and the anterior insula. Relationships were identified between resting-state functional connectivity alterations and the decrease in close social behaviour and increased astrogliosis.

conclusionsEarly-in-life anaesthesia exposure in NHPs is associated with resting-state functional connectivity alterations of the amygdala and the posterior cingulate cortex with other brain regions, evident at the juvenile age of 2 yr. These changes in resting-state functional connectivity correlate with the decrease in close social behaviour and increased astrogliosis. Using resting-state functional connectivity MRI to study the neuronal underpinnings of early-in-life anaesthesia-induced behavioural alterations could facilitate development of a biomarker for anaesthesia-induced developmental neurotoxicity.

Indexed as

IsofluraneAnimalsBrainBrain MappingGliosisGyrus CinguliMagnetic Resonance ImagingNeural PathwaysPrimatesIsofluraneamygdalaanaesthesiabrain developmentconnectivityneuroimagingneurotoxicitynon-human primatesposterior cingulate cortex

Identifiers

PMID37714750
PMCPMC10687619
OpenAlexW4386751442

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.