<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Gong B</submitter><funding>Guobing Chen</funding><pagination>531</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12899774</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(3)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Sepsis-induced organ dysfunction poses a significant clinical challenge with limited therapeutic options. This study investigated the therapeutic potential of the glucagon-like peptide-1 receptor agonist (GLP-1RA) liraglutide in sepsis and its underlying mechanisms, focusing on modulation of the gut microbiota-derived metabolome.&lt;h4>Methods&lt;/h4>Public transcriptomic data analysis identified overlapping targets between liraglutide and sepsis-related genes. In a murine cecal ligation and puncture (CLP) model, liraglutide treatment was evaluated for its effects on survival, systemic inflammation, and organ injury. The gut microbiota composition and fecal metabolome were assessed via 16S rRNA sequencing and UPLC-MS. We also measured plasma GLP-1 in sepsis patients and examin</pubmed_abstract><journal>Nutrients</journal><pubmed_title>GLP-1RA Liraglutide Attenuates Sepsis by Modulating Gut Microbiota and Associated Metabolites.</pubmed_title><pmcid>PMC12899774</pmcid><funding_grant_id>Yunnan Province Medical High-level Talents Program, L2024012</funding_grant_id><pubmed_authors>Gong B</pubmed_authors><pubmed_authors>Qi J</pubmed_authors><pubmed_authors>Chen G</pubmed_authors><pubmed_authors>Wang F</pubmed_authors><pubmed_authors>Shi Z</pubmed_authors><pubmed_authors>Su H</pubmed_authors></additional><is_claimable>false</is_claimable><name>GLP-1RA Liraglutide Attenuates Sepsis by Modulating Gut Microbiota and Associated Metabolites.</name><description>&lt;h4>Background&lt;/h4>Sepsis-induced organ dysfunction poses a significant clinical challenge with limited therapeutic options. This study investigated the therapeutic potential of the glucagon-like peptide-1 receptor agonist (GLP-1RA) liraglutide in sepsis and its underlying mechanisms, focusing on modulation of the gut microbiota-derived metabolome.&lt;h4>Methods&lt;/h4>Public transcriptomic data analysis identified overlapping targets between liraglutide and sepsis-related genes. In a murine cecal ligation and puncture (CLP) model, liraglutide treatment was evaluated for its effects on survival, systemic inflammation, and organ injury. The gut microbiota composition and fecal metabolome were assessed via 16S rRNA sequencing and UPLC-MS. We also measured plasma GLP-1 in sepsis patients and examin</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Feb</publication><modification>2026-07-09T13:20:34.172Z</modification><creation>2026-07-09T13:09:33.712Z</creation></dates><accession>S-EPMC12899774</accession><cross_references><pubmed>41683353</pubmed><doi>10.3390/nu18030531</doi></cross_references></HashMap>