<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yan F</submitter><funding>the Natural Science Foundation of Shandong Province</funding><funding>Research Fund for Lin He's Academician Workstation of New Medicine and Clinical Translation at Jining Medical University</funding><funding>Project of Medical and Health Technology Development Program in Shandong Province</funding><funding>National Natural Science Foundation of China</funding><funding>Shandong Training Program of Innovation and Entrepreneurship for Undergraduates</funding><funding>Project of Shandong Province Higher Educational Youth Innovation Science and Technology Program</funding><funding>Tai Shan Young Scholar Foundation of Shandong Province</funding><funding>Research Fund for Lin He’s Academician Workstation of New Medicine and Clinical Translation at Jining Medical University</funding><pagination>2274-2291</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12336090</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>48(4)</volume><pubmed_abstract>Sappanone A (SAP), a high-isoflavone compound derived from the traditional Chinese medicine Sumu, exhibits various pharmacological activities, including anti-inflammatory and anti-oxidant effects. However, its protective effects on the liver have rarely been reported. The aim of this study was to investigate the effects of SAP on immune-mediated liver injury induced by concanavalin A (Con A) in mice and to explore the underlying molecular mechanisms. Mice were administered SAP intraperitoneally (50 mg/kg body weight). Three hours later, Con A (18 mg/kg) was injected via the tail vein to induce liver damage. Livers and blood were collected 12 h after Con A challenge. Liver cell apoptosis, oxidative stress, and M1 macrophage activation in vivo were investigated. Bone marrow-derived macrophag</pubmed_abstract><journal>Inflammation</journal><pubmed_title>Sappanone A Ameliorates Concanavalin A-induced Immune-Mediated Liver Injury by Regulating M1 Macrophage Polarization.</pubmed_title><pmcid>PMC12336090</pmcid><funding_grant_id>S202410443201</funding_grant_id><funding_grant_id>82171810</funding_grant_id><funding_grant_id>202202070388</funding_grant_id><funding_grant_id>JYHL2022MS21</funding_grant_id><funding_grant_id>ZR2021MH287</funding_grant_id><funding_grant_id>ZR2023QH332</funding_grant_id><funding_grant_id>tsqn202211234</funding_grant_id><funding_grant_id>202202050678</funding_grant_id><funding_grant_id>2021KJ074</funding_grant_id><pubmed_authors>Guo Z</pubmed_authors><pubmed_authors>Li C</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Sun X</pubmed_authors><pubmed_authors>Zhong Z</pubmed_authors><pubmed_authors>Wang L</pubmed_authors><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Liu Z</pubmed_authors><pubmed_authors>Dong G</pubmed_authors><pubmed_authors>Gao M</pubmed_authors><pubmed_authors>Chen S</pubmed_authors><pubmed_authors>Yan F</pubmed_authors><pubmed_authors>Xiong H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Sappanone A Ameliorates Concanavalin A-induced Immune-Mediated Liver Injury by Regulating M1 Macrophage Polarization.</name><description>Sappanone A (SAP), a high-isoflavone compound derived from the traditional Chinese medicine Sumu, exhibits various pharmacological activities, including anti-inflammatory and anti-oxidant effects. However, its protective effects on the liver have rarely been reported. The aim of this study was to investigate the effects of SAP on immune-mediated liver injury induced by concanavalin A (Con A) in mice and to explore the underlying molecular mechanisms. Mice were administered SAP intraperitoneally (50 mg/kg body weight). Three hours later, Con A (18 mg/kg) was injected via the tail vein to induce liver damage. Livers and blood were collected 12 h after Con A challenge. Liver cell apoptosis, oxidative stress, and M1 macrophage activation in vivo were investigated. Bone marrow-derived macrophag</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-04-30T14:37:20.065Z</modification><creation>2026-04-07T16:03:40.376Z</creation></dates><accession>S-EPMC12336090</accession><cross_references><pubmed>39589634</pubmed><doi>10.1007/s10753-024-02189-x</doi></cross_references></HashMap>