Evidence map›Paper›PMID 39078595›Full record

ArticleNeuroscience bulletin2024

Triggering Receptor Expressed on Myeloid Cells 2 Alleviated Sevoflurane-Induced Developmental Neurotoxicity via Microglial Pruning of Dendritic Spines in the CA1 Region of the Hippocampus.

Li Deng, Shao-Yong Song, Wei-Ming Zhao, Xiao-Wen Meng, Hong Liu, Qing Zheng, Ke Peng, Fu-Hai Ji

Abstract read
In one paragraph

Article in Neuroscience bulletin, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Restoration of Extrasynaptic/Synaptic GABANeuroscience bulletin · 2026
    Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. 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

8 authors.

Li Deng *Department of Anaesthesiology, The First Affiliated Hospital of Soochow University, Suzhou, 215006, China.ORCID http://orcid.org/0000-0001-5447-4058
Shao-Yong Song *Department of Anaesthesiology, The First Affiliated Hospital of Soochow University, Suzhou, 215006, China.ORCID http://orcid.org/0000-0002-0483-0760
Wei-Ming ZhaoDepartment of Anaesthesiology, The First Affiliated Hospital of Soochow University, Suzhou, 215006, China.ORCID http://orcid.org/0000-0001-6238-1679
Xiao-Wen MengDepartment of Anaesthesiology, The First Affiliated Hospital of Soochow University, Suzhou, 215006, China.ORCID http://orcid.org/0000-0001-6961-8683
Hong LiuDepartment of Anaesthesiology and Pain Medicine, University of California Davis Health, Sacramento, CA, USA.ORCID http://orcid.org/0000-0003-3611-7131
Qing ZhengCenter for Molecular Imaging and Nuclear Medicine, Collaborative Innovation Center of Radiation Medicine of Jiangsu Higher Education, State Key Laboratory of Radiation Medicine and Protection, School for Radiological and Interdisciplinary Sciences (RAD-X), Suzhou Medical College of Soochow University, Suzhou, 215006, China.
Ke PengDepartment of Anaesthesiology, The First Affiliated Hospital of Soochow University, Suzhou, 215006, China. pengke0422@163.com.ORCID http://orcid.org/0000-0003-2879-1759
Fu-Hai JiDepartment of Anaesthesiology, The First Affiliated Hospital of Soochow University, Suzhou, 215006, China. jifuhaisuda@163.com.ORCID http://orcid.org/0000-0001-6649-665X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sevoflurane induces developmental neurotoxicity in mice; however, the underlying mechanisms remain unclear. Triggering receptor expressed on myeloid cells 2 (TREM2) is essential for microglia-mediated synaptic refinement during the early stages of brain development. We explored the effects of TREM2 on dendritic spine pruning during sevoflurane-induced developmental neurotoxicity in mice. Mice were anaesthetized with sevoflurane on postnatal days 6, 8, and 10. Behavioral performance was assessed using the open field test and Morris water maze test. Genetic knockdown of TREM2 and overexpression of TREM2 by stereotaxic injection were used for mechanistic experiments. Western blotting, immunofluorescence, electron microscopy, three-dimensional reconstruction, Golgi staining, and whole-cell patch-clamp recordings were performed. Sevoflurane exposures upregulated the protein expression of TREM2, increased microglia-mediated pruning of dendritic spines, and reduced synaptic multiplicity and excitability of CA1 neurons. TREM2 genetic knockdown significantly decreased dendritic spine pruning, and partially aggravated neuronal morphological abnormalities and cognitive impairments in sevoflurane-treated mice. In contrast, TREM2 overexpression enhanced microglia-mediated pruning of dendritic spines and rescued neuronal morphological abnormalities and cognitive dysfunction. TREM2 exerts a protective role against neurocognitive impairments in mice after neonatal exposures to sevoflurane by enhancing microglia-mediated pruning of dendritic spines in CA1 neurons. This provides a potential therapeutic target in the prevention of sevoflurane-induced developmental neurotoxicity.

Indexed as

CA1 Region, HippocampalDendritic SpinesMembrane GlycoproteinsMicrogliaReceptors, ImmunologicSevofluraneAnesthetics, InhalationAnimalsCognitive DysfunctionMaleMiceMice, Inbred C57BLNeuronal PlasticityNeurotoxicity SyndromesAnesthetics, InhalationMembrane GlycoproteinsReceptors, ImmunologicSevofluraneTrem2 protein, mouseCA1 neuronsDendritic spinesDevelopmental neurotoxicityMicrogliaSevofluraneTREM2

Identifiers

PMID39078595
PMCPMC11365924

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.