Evidence map›Paper›PMID 41567523›Full record

ArticleAnesthesiology and perioperative science2026

Neurophysiological differences between dexmedetomidine sedation and natural sleep across the rodent lifespan: implications for aging and perioperative brain health.

Morgan J Siegmann, Daniel P Zachs, Jonathan D Kenny, Arianna R S Lark, Fayaz A Mir, Eric D Melonakos, Mohsen Hozan, Sarah Toledano, Rebecca R Goldblum, Yang Liu and 10 more

Abstract read
In one paragraph

Article in Anesthesiology and perioperative science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

20 authors.

Morgan J SiegmannMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA USA.
Daniel P ZachsDepartment of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA USA.
Jonathan D KennyMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA USA.
Arianna R S LarkMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA USA.
Fayaz A MirMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA USA.
Eric D MelonakosMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA USA.
Mohsen HozanDepartment of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA USA.
Sarah ToledanoDepartment of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA USA.
Rebecca R GoldblumDepartment of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA USA.
Yang LiuDepartment of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA USA.
Michael A NolanDepartment of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA USA.
Gabriella CohenMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA USA.
Jinyoung ChoiMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA USA.
Christian G WhiteMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA USA.
Eliza A CrowleyMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA USA.
Abigail Hardy CarpenterMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA USA.
Bryton A ToroMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA USA.
Channing E SymeMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA USA.
Emery N BrownMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA USA.
Christa J NehsMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA USA.ORCID 0000-0002-6708-1656

Funding

TRAINING IN SLEEP, CIRCADIAN &RESPIRATORY NEUROBIOLOGYT32HL007901 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI Charles A Czeisler · 1998 to 2026
$18.5M
Redesigning General Anesthesia (Admin Supp)R01GM104948 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BOYDEN, EDWARD S., BROWN, EMERY N · 2012 to 2016
$4.4M
NHLBI NIH HHS T32 HL007901NIGMS NIH HHS R01 GM104948
6 · The paper itself

Abstract

Purpose: Dexmedetomidine is commonly used for its sedative and neuroprotective effects, but its impact on brain activity and sleep architecture is not fully understood. Emerging evidence suggests it may improve postoperative outcomes, particularly in older adults, by promoting sleep-like states with stable hemodynamics, reducing posttraumatic stress, and decreasing delirium. This study aims to better characterize the neurophysiological profile of dexmedetomidine-induced sedation by comparing it to natural sleep in both young and aged mice. Methods: Twelve 4-5 month old and six 10-18-month-old C57BL/6 J male mice were used. Animals were implanted with electroencephalography/electromyography electrodes. After at least 7 days of recovery, animals received intraperitoneal injections of saline or dexmedetomidine (50-400 µg/kg) and sleep-wake states were recorded for 5-12 h. Results: Dexmedetomidine significantly increased delta (0.5-4 Hz) power beyond levels observed during natural non-rapid eye movement (NREM) sleep, followed by suppression of both high frequency (> 10 Hz) electroencephalography activity and REM sleep in a dose dependent manner. Body posture was sprawled during dexmedetomidine versus curled as during natural sleep. Notably, at the transition into sedation, dexmedetomidine induced high-voltage spikes resembling high-voltage spindles and spike wave discharges. These spikes were more prominent in the prefrontal cortex compared to the parietal cortex and aged animals exhibited more high voltage spikes than young adult animals. Conclusion: The combination of elevated delta power, high-voltage spikes, suppression of high-frequency activity, and sprawled body posture during dexmedetomidine-induced sedation indicates a state of unconsciousness that is neurophysiologically distinct from natural NREM sleep in mice. These findings highlight important age-related differential responses to dexmedetomidine and help inform its safe and effective use in vulnerable patient populations.

Indexed as

Epileptiform activityHigh voltage spindleSpike wave discharge

Identifiers

PMID41567523
PMCPMC12816052

What OpenQuestion holds

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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.