<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Hu M</submitter><pubmed_abstract>This study investigated the protective properties and mechanisms of D-mannose against hepatic steatosis in experimental alcoholic liver disease (ALD). Drinking-water supplementation of D-mannose significantly attenuated hepatic steatosis in a standard mouse ALD model established by chronic-binge ethanol feeding, especially hepatocyte lipid deposition. This function of D-mannose on lipid accumulation in hepatocytes was also confirmed using ethanol-treated primary mouse hepatocytes (PMHs) with a D-mannose supplement. Meanwhile, D-mannose regulated lipid metabolism by rescuing ethanol-mediated reduction of fatty acid oxidation genes (PPARα, ACOX1, CPT1) and elevation of lipogenic genes (SREBP1c, ACC1, FASN). PI3K/Akt/mTOR signaling pathway was involved in this effect of D-mannose on lipid met</pubmed_abstract><journal>Frontiers in immunology</journal><pagination>877650</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9021718</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>D-Mannose Regulates Hepatocyte Lipid Metabolism &lt;i>via&lt;/i> PI3K/Akt/mTOR Signaling Pathway and Ameliorates Hepatic Steatosis in Alcoholic Liver Disease.</pubmed_title><pmcid>PMC9021718</pmcid><pubmed_authors>Chang B</pubmed_authors><pubmed_authors>Luo J</pubmed_authors><pubmed_authors>Lu X</pubmed_authors><pubmed_authors>Chen Z</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Hu M</pubmed_authors><pubmed_authors>Dong L</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Deng F</pubmed_authors><pubmed_authors>Zhou J</pubmed_authors></additional><is_claimable>false</is_claimable><name>D-Mannose Regulates Hepatocyte Lipid Metabolism &lt;i>via&lt;/i> PI3K/Akt/mTOR Signaling Pathway and Ameliorates Hepatic Steatosis in Alcoholic Liver Disease.</name><description>This study investigated the protective properties and mechanisms of D-mannose against hepatic steatosis in experimental alcoholic liver disease (ALD). Drinking-water supplementation of D-mannose significantly attenuated hepatic steatosis in a standard mouse ALD model established by chronic-binge ethanol feeding, especially hepatocyte lipid deposition. This function of D-mannose on lipid accumulation in hepatocytes was also confirmed using ethanol-treated primary mouse hepatocytes (PMHs) with a D-mannose supplement. Meanwhile, D-mannose regulated lipid metabolism by rescuing ethanol-mediated reduction of fatty acid oxidation genes (PPARα, ACOX1, CPT1) and elevation of lipogenic genes (SREBP1c, ACC1, FASN). PI3K/Akt/mTOR signaling pathway was involved in this effect of D-mannose on lipid met</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-04T12:56:12.929Z</modification><creation>2025-04-04T12:56:12.929Z</creation></dates><accession>S-EPMC9021718</accession><cross_references><pubmed>35464439</pubmed><doi>10.3389/fimmu.2022.877650</doi></cross_references></HashMap>