<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Bai Z</submitter><pubmed_abstract>&lt;b>Background:&lt;/b> Xiao-Yao-San (XYS) is a traditional Chinese prescription that regulates gastrointestinal function, improves mental and psychological abnormalities, and enhances liver function. However, the underlying mechanism of XYS for relieving anti-tuberculosis (AT) drug-induced liver injury is not clear. &lt;b>Objective:&lt;/b> The current study examined whether XYS alleviated the symptoms of AT drug-induced liver injury in mice via the mitochondrial oxidative stress pathway. &lt;b>Methods:&lt;/b> BALB/c male mice were randomly divided into four groups of 12 animals, including a control group, a model group, a 0.32 g/kg XYS group, and a 0.64 g/kg XYS group. The effect of XYS on the degree of liver injury was observed using haematoxylin and eosin staining (HE) and oil red O staining of patholog</pubmed_abstract><journal>Frontiers in pharmacology</journal><pagination>948128</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9475289</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Xiao-Yao-San protects against anti-tuberculosis drug-induced liver injury by regulating Grsf1 in the mitochondrial oxidative stress pathway.</pubmed_title><pmcid>PMC9475289</pmcid><pubmed_authors>Tao W</pubmed_authors><pubmed_authors>Yu S</pubmed_authors><pubmed_authors>Cao Y</pubmed_authors><pubmed_authors>Bai Z</pubmed_authors><pubmed_authors>Zhou Y</pubmed_authors><pubmed_authors>Shi Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Xiao-Yao-San protects against anti-tuberculosis drug-induced liver injury by regulating Grsf1 in the mitochondrial oxidative stress pathway.</name><description>&lt;b>Background:&lt;/b> Xiao-Yao-San (XYS) is a traditional Chinese prescription that regulates gastrointestinal function, improves mental and psychological abnormalities, and enhances liver function. However, the underlying mechanism of XYS for relieving anti-tuberculosis (AT) drug-induced liver injury is not clear. &lt;b>Objective:&lt;/b> The current study examined whether XYS alleviated the symptoms of AT drug-induced liver injury in mice via the mitochondrial oxidative stress pathway. &lt;b>Methods:&lt;/b> BALB/c male mice were randomly divided into four groups of 12 animals, including a control group, a model group, a 0.32 g/kg XYS group, and a 0.64 g/kg XYS group. The effect of XYS on the degree of liver injury was observed using haematoxylin and eosin staining (HE) and oil red O staining of patholog</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-27T03:22:46.943Z</modification><creation>2024-11-14T20:09:36.533Z</creation></dates><accession>S-EPMC9475289</accession><cross_references><pubmed>36120303</pubmed><doi>10.3389/fphar.2022.948128</doi></cross_references></HashMap>