<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>34(9)</volume><submitter>Shin J</submitter><pubmed_abstract>Alcohol consumption causes severe liver damage and oxidative stress. This study investigated the hepatoprotective effects of enzymatic porcine placenta hydrolysate (EPPH) in Sprague-Dawley rats under acute alcohol administration. EPPH significantly reduced plasma ethanol and acetaldehyde levels in a dose-dependent manner. Furthermore, EPPH decreased the hepatic levels of malondialdehyde and thiobarbituric acid reactive substances and suppressed &lt;i>Cyp2e1&lt;/i> mRNA expression. EPPH decreased the plasma alanine transaminase and aspartate transaminase levels and increased the hepatic NAD&lt;sup>+&lt;/sup>/NADH ratio. Hepatic transcriptome analysis revealed the significant regulation of key genes involved in inflammation, alcohol response, and apoptosis. Phosphokinase array analysis demonstrated that</pubmed_abstract><journal>Food science and biotechnology</journal><pagination>2025-2038</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11972273</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Activation of hepatic alcohol metabolism by enzymatic porcine placenta hydrolysate in rats.</pubmed_title><pmcid>PMC11972273</pmcid><pubmed_authors>Ju SH</pubmed_authors><pubmed_authors>Lee SJ</pubmed_authors><pubmed_authors>Yoon SM</pubmed_authors><pubmed_authors>Shin J</pubmed_authors><pubmed_authors>Sim D</pubmed_authors><pubmed_authors>Kim Y</pubmed_authors><pubmed_authors>Lee Y</pubmed_authors><pubmed_authors>Yoo H</pubmed_authors><pubmed_authors>Jung YJ</pubmed_authors><pubmed_authors>Kim JS</pubmed_authors><pubmed_authors>Bae GW</pubmed_authors></additional><is_claimable>false</is_claimable><name>Activation of hepatic alcohol metabolism by enzymatic porcine placenta hydrolysate in rats.</name><description>Alcohol consumption causes severe liver damage and oxidative stress. This study investigated the hepatoprotective effects of enzymatic porcine placenta hydrolysate (EPPH) in Sprague-Dawley rats under acute alcohol administration. EPPH significantly reduced plasma ethanol and acetaldehyde levels in a dose-dependent manner. Furthermore, EPPH decreased the hepatic levels of malondialdehyde and thiobarbituric acid reactive substances and suppressed &lt;i>Cyp2e1&lt;/i> mRNA expression. EPPH decreased the plasma alanine transaminase and aspartate transaminase levels and increased the hepatic NAD&lt;sup>+&lt;/sup>/NADH ratio. Hepatic transcriptome analysis revealed the significant regulation of key genes involved in inflammation, alcohol response, and apoptosis. Phosphokinase array analysis demonstrated that</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 May</publication><modification>2026-07-16T18:26:57.212Z</modification><creation>2026-07-09T11:14:35.826Z</creation></dates><accession>S-EPMC11972273</accession><cross_references><pubmed>40196334</pubmed><doi>10.1007/s10068-025-01822-1</doi></cross_references></HashMap>