<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>2023</volume><submitter>Qi Z</submitter><pubmed_abstract>There remains a lack of standard models that have all the characteristics of human diseases. Especially in immunological hepatic fibrosis, the bovine serum albumin (BSA)-induced liver fibrosis models have the same developmental mechanisms as human liver fibrosis models, but have received little attention. We standardized a BSA-induced liver fibrosis model in rats and thoroughly assessed its pathological characteristics. We also used 16S sequencing to assess homeostasis of the intestinal microflora of rats with BSA-induced liver fibrosis and detected various differential metabolites in the serum of these rats using ultrahigh-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). We observed stable and unambiguous histological changes in liver tissue morphology and remarka</pubmed_abstract><journal>Journal of immunology research</journal><pagination>5577850</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10539088</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Alterations in the "Gut-Liver Axis" on Rats with Immunological Hepatic Fibrosis.</pubmed_title><pmcid>PMC10539088</pmcid><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Qi Z</pubmed_authors><pubmed_authors>Li D</pubmed_authors><pubmed_authors>Qi X</pubmed_authors><pubmed_authors>Cong M</pubmed_authors><pubmed_authors>Sun H</pubmed_authors><pubmed_authors>Liu T</pubmed_authors><pubmed_authors>Xu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Alterations in the "Gut-Liver Axis" on Rats with Immunological Hepatic Fibrosis.</name><description>There remains a lack of standard models that have all the characteristics of human diseases. Especially in immunological hepatic fibrosis, the bovine serum albumin (BSA)-induced liver fibrosis models have the same developmental mechanisms as human liver fibrosis models, but have received little attention. We standardized a BSA-induced liver fibrosis model in rats and thoroughly assessed its pathological characteristics. We also used 16S sequencing to assess homeostasis of the intestinal microflora of rats with BSA-induced liver fibrosis and detected various differential metabolites in the serum of these rats using ultrahigh-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). We observed stable and unambiguous histological changes in liver tissue morphology and remarka</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2026-06-04T09:49:29.827Z</modification><creation>2025-06-01T12:36:58.007Z</creation></dates><accession>S-EPMC10539088</accession><cross_references><pubmed>37781475</pubmed><doi>10.1155/2023/5577850</doi></cross_references></HashMap>