<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhao T</submitter><funding>National Natural Science Foundation</funding><funding>Beijing, Guangzhou Institute of Pediatrics/ Guangzhou Women and Children's Medical Center funds</funding><funding>Guangzhou Municipal Science and Technology Program</funding><funding>Beijing, Guangzhou Institute of Pediatrics/ Guangzhou Women and Children&amp;apos;s Medical Center funds</funding><pagination>2369-2380</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9890293</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(12)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>GABAergic deficits have been considered to be associated with the pathophysiology of schizophrenia, and hence, GABA receptors subtype A (GABA&lt;sub>A&lt;/sub>Rs) modulators, such as commonly used volatile anesthetic sevoflurane, may have therapeutic values for schizophrenia. The present study investigates the therapeutic effectiveness of low-concentration sevoflurane in MK801-induced schizophrenia-like mice and schizophrenia patients.&lt;h4>Methods&lt;/h4>Three weeks after MK801 administration (0.5 mg kg&lt;sup>-1&lt;/sup>, i.p. twice a day for 5 days), mice were exposed to 1% sevoflurane 1hr/day for 5 days. Behavioral tests, immunohistochemical analysis, western blot assay, and electrophysiology assessments were performed 1-week post-exposure. Ten schizophrenia patients received 1% sevo</pubmed_abstract><journal>Current neuropharmacology</journal><pubmed_title>Sevoflurane Ameliorates Schizophrenia in a Mouse Model and Patients: A Pre-Clinical and Clinical Feasibility Study.</pubmed_title><pmcid>PMC9890293</pmcid><funding_grant_id>81870823</funding_grant_id><funding_grant_id>GCP-2019-002</funding_grant_id><funding_grant_id>81671116</funding_grant_id><funding_grant_id>GCP-2018-001</funding_grant_id><funding_grant_id>GCP-2018-001, GCP-2019-002</funding_grant_id><funding_grant_id>81671116, 81870823</funding_grant_id><funding_grant_id>201803010025</funding_grant_id><pubmed_authors>Wu L</pubmed_authors><pubmed_authors>Zhou Q</pubmed_authors><pubmed_authors>Lin C</pubmed_authors><pubmed_authors>Qin J</pubmed_authors><pubmed_authors>Zhao T</pubmed_authors><pubmed_authors>Shi Z</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Ma D</pubmed_authors><pubmed_authors>Song X</pubmed_authors><pubmed_authors>Ling N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Sevoflurane Ameliorates Schizophrenia in a Mouse Model and Patients: A Pre-Clinical and Clinical Feasibility Study.</name><description>&lt;h4>Background&lt;/h4>GABAergic deficits have been considered to be associated with the pathophysiology of schizophrenia, and hence, GABA receptors subtype A (GABA&lt;sub>A&lt;/sub>Rs) modulators, such as commonly used volatile anesthetic sevoflurane, may have therapeutic values for schizophrenia. The present study investigates the therapeutic effectiveness of low-concentration sevoflurane in MK801-induced schizophrenia-like mice and schizophrenia patients.&lt;h4>Methods&lt;/h4>Three weeks after MK801 administration (0.5 mg kg&lt;sup>-1&lt;/sup>, i.p. twice a day for 5 days), mice were exposed to 1% sevoflurane 1hr/day for 5 days. Behavioral tests, immunohistochemical analysis, western blot assay, and electrophysiology assessments were performed 1-week post-exposure. Ten schizophrenia patients received 1% sevo</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-26T13:33:50.307Z</modification><creation>2025-04-06T14:14:53.141Z</creation></dates><accession>S-EPMC9890293</accession><cross_references><pubmed>35272593</pubmed><doi>10.2174/1570159X20666220310115846</doi></cross_references></HashMap>