Evidence map›Paper›PMID 38177340›Full record

ArticleNature neuroscience2024

Microglia enhance post-anesthesia neuronal activity by shielding inhibitory synapses.

Koichiro Haruwaka, Yanlu Ying, Yue Liang, Anthony D Umpierre, Min-Hee Yi, Vaclav Kremen, Tingjun Chen, Tao Xie, Fangfang Qi, Shunyi Zhao and 5 more

Open access · greenAbstract read
In one paragraph

Article in Nature neuroscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
14.8field-weighted citation impact, top 1% 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

45 citing papers in PubMed, 60 citations in OpenAlex.

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  15. Microglia Modulate Information Processing in the Mouse Barrel Cortex.The Journal of neuroscience : the official journal of the Society for Neuroscience · 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

15 authors at 5 institutions in 3 countries.

Koichiro Haruwaka *Department of Neurology, Mayo Clinic, Rochester, MN, USA.ORCID http://orcid.org/0000-0003-1484-6990
Yanlu Ying *Department of Anesthesiology, Guangzhou First People's Hospital, South China University of Technology, Guangzhou, China. eyyingyanlu@scut.edu.cn.ORCID http://orcid.org/0000-0001-6088-124X
Yue LiangDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
Anthony D UmpierreDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.ORCID http://orcid.org/0000-0002-1470-8881
Min-Hee YiDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.ORCID http://orcid.org/0000-0003-2066-3584
Vaclav KremenDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.ORCID http://orcid.org/0000-0001-9844-7617
Tingjun ChenDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
Tao XieTranslational Oncology Group, Faculty of Science, School of Life Sciences, University of Technology Sydney, Sydney, New South Wales, Australia.ORCID http://orcid.org/0000-0002-0580-6877
Fangfang QiDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
Shunyi ZhaoDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.ORCID http://orcid.org/0000-0001-7265-0801
Jiaying ZhengDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
Yong U LiuDepartment of Anesthesiology, Guangzhou First People's Hospital, South China University of Technology, Guangzhou, China.
Hailong DongDepartment of Anesthesiology and Perioperative Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, China.ORCID http://orcid.org/0000-0001-8984-9067
Gregory A WorrellDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.ORCID http://orcid.org/0000-0003-2916-0553
Long-Jun WuDepartment of Neurology, Mayo Clinic, Rochester, MN, USA. wu.longjun@mayo.edu.ORCID http://orcid.org/0000-0001-8019-3380
Mayo Clinic in Arizona · USGuangzhou First People's Hospital · CNMayo Clinic · USUniversity of Technology Sydney · AUXijing Hospital · CN

Funding

Project 4 (Genetic modifiers for APOE-associated Alzheimer's disease pathogenesis)U19AG069701 · NIA · MAYO CLINIC JACKSONVILLE · PI Na Zhao · 2021 to 2026
$42.0M
The glial mechanism for electrical brain stimulationR01NS112144 · NINDS · MAYO CLINIC ROCHESTER · PI WANG, HAI-LONG, WORRELL, GREGORY A · 2019 to 2023
$3.8M
The Role of Microglia in EpilepsyR01NS088627 · NINDS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI WU, LONG-JUN · 2014 to 2023
$3.6M
How microglia sense and regulate neuronal activity in the adult brainR35NS132326 · NINDS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Long-Jun Wu · 2023 to 2026
$3.2M
Microglial regulation of neuronal activity in TDP-43 neurodegenerationRF1AG082314 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI WU, LONG-JUN · 2023 to 2023
$1.9M
Optimizing Pharmacotherapy with Noninvasive Wearable Sensors and Subscalp EEGUH3NS123066 · NINDS · MAYO CLINIC ROCHESTER · PI Benjamin H Brinkmann, Gregory A Worrell · 2025 to 2026
$1.4M
Microglial regulation of neuronal activity in TDP-43 neurodegenerationR01AG082314 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Long-Jun Wu · 2026 to 2026
$712k
NIA NIH HHS R01 AG082314NIA NIH HHS RF1 AG082314NIA NIH HHS U19 AG069701NINDS NIH HHS R01 NS088627NINDS NIH HHS R01 NS112144NINDS NIH HHS R35 NS132326NINDS NIH HHS UH3 NS123066
6 · The paper itself

Abstract

Microglia are resident immune cells of the central nervous system and play key roles in brain homeostasis. During anesthesia, microglia increase their dynamic process surveillance and interact more closely with neurons. However, the functional significance of microglial process dynamics and neuronal interaction under anesthesia is largely unknown. Using in vivo two-photon imaging in mice, we show that microglia enhance neuronal activity after the cessation of isoflurane anesthesia. Hyperactive neuron somata are contacted directly by microglial processes, which specifically colocalize with GABAergic boutons. Electron-microscopy-based synaptic reconstruction after two-photon imaging reveals that, during anesthesia, microglial processes enter into the synaptic cleft to shield GABAergic inputs. Microglial ablation or loss of microglial β2-adrenergic receptors prevents post-anesthesia neuronal hyperactivity. Our study demonstrates a previously unappreciated function of microglial process dynamics, which enable microglia to transiently boost post-anesthesia neuronal activity by physically shielding inhibitory inputs.

Indexed as

AnesthesiaMicrogliaAnimalsBrainMiceNeuronsSynapses

Identifiers

PMID38177340
PMCPMC10960525
OpenAlexW4390581844

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.