Evidence map›Paper›PMID 35272593›Full record

ArticleCurrent neuropharmacology2022

Sevoflurane Ameliorates Schizophrenia in a Mouse Model and Patients: A Pre-Clinical and Clinical Feasibility Study.

Tianyun Zhao, Ziwen Shi, Nongxi Ling, Jingwen Qin, Quancai Zhou, Lingzhi Wu, Yuansheng Wang, Chuansong Lin, Daqing Ma, Xingrong Song

Open access · greenAbstract read
In one paragraph

Article in Current neuropharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 39% 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

5 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. 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

10 authors at 4 institutions in 2 countries.

Tianyun ZhaoDepartment of Anesthesiology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Ziwen ShiDepartment of Anesthesiology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Nongxi LingDepartment of Psychiatry, The Third People\'s Hospital of Xinhui District, Guangdong, China.
Jingwen QinDepartment of Anesthesiology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Quancai ZhouDepartment of Psychiatry, The Third People\'s Hospital of Xinhui District, Guangdong, China.
Lingzhi WuDivision of Anaesthetics, Pain Medicine & Intensive Care, Department of Surgery & Cancer, Faculty of Medicine, Imperial College London, Chelsea and Westminster Hospital, London, UK.
Yuansheng WangDepartment of Anesthesiology, Jiangmen Central Hospital, Affiliated Jiangmen Hospital of Sun Yat-sen University, Guangdong, China.
Chuansong LinDepartment of Psychiatry, The Third People\'s Hospital of Xinhui District, Guangdong, China.
Daqing MaDivision of Anaesthetics, Pain Medicine & Intensive Care, Department of Surgery & Cancer, Faculty of Medicine, Imperial College London, Chelsea and Westminster Hospital, London, UK.
Xingrong SongDepartment of Anesthesiology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Guangzhou Medical University · CNXinhui People's Hospital · CNChelsea and Westminster Hospital · GBSun Yat-sen University · CN

Funding

Beijing, Guangzhou Institute of Pediatrics/ Guangzhou Women and Children's Medical Center funds GCP-2018-001, GCP-2019-002Guangzhou Municipal Science and Technology Program 201803010025National Natural Science Foundation 81671116, 81870823
6 · The paper itself

Abstract

backgroundGABAergic deficits have been considered to be associated with the pathophysiology of schizophrenia, and hence, GABA receptors subtype A (GABA

methodsThree weeks after MK801 administration (0.5 mg kg

resultsMK801 induced hypolocomotion and social deficits, downregulated expression of NMDARs subunits and postsynaptic density protein 95 (PSD95), reduced parvalbumin - and GAD67-positive neurons, altered amplitude and frequency of mEPSCs and mIPSCs, and increased the excitation/inhibition ratio. All these changes induced by MK-801 were attenuated by sevoflurane administration. Six and eight patients achieved a response defined as a reduction of at least 30% in the PANSS total score at 1st and 2nd week after treatments. The BPRS-18 total score was found to be significantly decreased by 38% at the 2nd week (p < 0.01).

conclusionLow-concentration sevoflurane effectively reversed MK801-induced schizophrenialike disease in mice and alleviated schizophrenia patients' symptoms. Our work suggests sevoflurane to be a valuable therapeutic strategy for treating schizophrenia patients.

Indexed as

Dizocilpine MaleateSchizophreniaAnimalsFeasibility StudiesMiceNeuronsSevofluraneDizocilpine MaleateSevofluraneearly responseE/I balanceLow-concentrationschizophrenia.sevofluranesocial deficits

Identifiers

PMID35272593
PMCPMC9890293
OpenAlexW4220809498

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.