<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bilinsky LM</submitter><funding>National Institute of Environmental Health Sciences</funding><funding>NIEHS NIH HHS</funding><funding>U.S. Food and Drug Administration</funding><pagination>100299</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11044893</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>29</volume><pubmed_abstract>This paper presents an ordinary differential equation (ODE) model of endogenous H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub> production and elimination in hepatocytes that is unique, at the time of writing, in its ability to accurately compute intracellular H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub> concentration during incidents of oxidative stress and in its usefulness for constructing PBPK/PD models for ROS-generating xenobiotics. Versions of the model are presented for rat hepatocytes &lt;i>in vitro&lt;/i> and mouse liver &lt;i>in vivo&lt;/i>. A generic method is given for using the model to create PBPK/PD models which predict intracellular H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub> concentration and oxidative-stress-induced hepatocyte death; these are identifiable from &lt;i>in vitro&lt;/i> data sets reporting cell mortality following xenobiotic expos</pubmed_abstract><journal>Computational toxicology (Amsterdam, Netherlands)</journal><pubmed_title>A Computational Model of Endogenous Hydrogen Peroxide Metabolism in Hepatocytes, Featuring a Critical Role for GSH.</pubmed_title><pmcid>PMC11044893</pmcid><funding_grant_id>12013</funding_grant_id><funding_grant_id>Y01 S12013001</funding_grant_id><funding_grant_id>FDA IAG #224-17-0502</funding_grant_id><pubmed_authors>Bilinsky LM</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Computational Model of Endogenous Hydrogen Peroxide Metabolism in Hepatocytes, Featuring a Critical Role for GSH.</name><description>This paper presents an ordinary differential equation (ODE) model of endogenous H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub> production and elimination in hepatocytes that is unique, at the time of writing, in its ability to accurately compute intracellular H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub> concentration during incidents of oxidative stress and in its usefulness for constructing PBPK/PD models for ROS-generating xenobiotics. Versions of the model are presented for rat hepatocytes &lt;i>in vitro&lt;/i> and mouse liver &lt;i>in vivo&lt;/i>. A generic method is given for using the model to create PBPK/PD models which predict intracellular H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub> concentration and oxidative-stress-induced hepatocyte death; these are identifiable from &lt;i>in vitro&lt;/i> data sets reporting cell mortality following xenobiotic expos</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2025-04-04T02:46:45.219Z</modification><creation>2025-04-04T02:46:45.219Z</creation></dates><accession>S-EPMC11044893</accession><cross_references><pubmed>38682127</pubmed><doi>10.1016/j.comtox.2024.100299</doi></cross_references></HashMap>