<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>118</volume><submitter>Kuhre RE</submitter><funding>Novo Nordisk</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>Amycretin is a novel unimolecular glucagon-like peptide-1 (GLP-1) and amylin receptor agonist. This study aimed to determine its role in mitigating diet-induced metabolic disorders, such as obesity, insulin resistance, and fatty liver disease, in mice and rats.&lt;h4>Methods&lt;/h4>Preclinical studies were conducted to characterise amycretin activation of GLP-1, amylin and calcitonin receptors, and determine the effects of amycretin administration on the metabolic health of mice and rats. Investigations included measurements of body weight and body composition, energy intake and energy expenditure, insulin sensitivity, metabolic dysfunction-associated steatotic liver disease (MASLD), and access in the mouse brain.&lt;h4>Findings&lt;/h4>Amycretin activated human, mouse and rat GLP-1,</pubmed_abstract><journal>EBioMedicine</journal><pagination>105862</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12309853</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The effect of amycretin, a unimolecular glucagon-like peptide-1 and amylin receptor agonist, on body weight and metabolic dysfunction in mice and rats.</pubmed_title><pmcid>PMC12309853</pmcid><pubmed_authors>Ipsen DH</pubmed_authors><pubmed_authors>Lundh S</pubmed_authors><pubmed_authors>Hjollund KR</pubmed_authors><pubmed_authors>Madsen KG</pubmed_authors><pubmed_authors>Hogendorf WFJ</pubmed_authors><pubmed_authors>Raun K</pubmed_authors><pubmed_authors>Secher A</pubmed_authors><pubmed_authors>Ballarin-Gonzalez B</pubmed_authors><pubmed_authors>Petersen SB</pubmed_authors><pubmed_authors>Brand CL</pubmed_authors><pubmed_authors>Glendorf T</pubmed_authors><pubmed_authors>Kruse T</pubmed_authors><pubmed_authors>Vegge A</pubmed_authors><pubmed_authors>Kuhre RE</pubmed_authors></additional><is_claimable>false</is_claimable><name>The effect of amycretin, a unimolecular glucagon-like peptide-1 and amylin receptor agonist, on body weight and metabolic dysfunction in mice and rats.</name><description>&lt;h4>Background&lt;/h4>Amycretin is a novel unimolecular glucagon-like peptide-1 (GLP-1) and amylin receptor agonist. This study aimed to determine its role in mitigating diet-induced metabolic disorders, such as obesity, insulin resistance, and fatty liver disease, in mice and rats.&lt;h4>Methods&lt;/h4>Preclinical studies were conducted to characterise amycretin activation of GLP-1, amylin and calcitonin receptors, and determine the effects of amycretin administration on the metabolic health of mice and rats. Investigations included measurements of body weight and body composition, energy intake and energy expenditure, insulin sensitivity, metabolic dysfunction-associated steatotic liver disease (MASLD), and access in the mouse brain.&lt;h4>Findings&lt;/h4>Amycretin activated human, mouse and rat GLP-1,</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jul</publication><modification>2026-03-27T15:28:59.059Z</modification><creation>2025-08-24T03:06:52.178Z</creation></dates><accession>S-EPMC12309853</accession><cross_references><pubmed>40706446</pubmed><doi>10.1016/j.ebiom.2025.105862</doi></cross_references></HashMap>