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ABSTRACT: Purpose
The objective of this study was to develop and produce a novel fusion protein that combines GLP-1 (glucagon-like peptide-1) and FGF21 (fibroblast growth factor 21), with the aim of achieving synergistic pharmacological effects through the targeting of dual pathways, followed by validation of these effects in a non-alcoholic steatohepatitis (NASH) model.Methods
We utilized C57Bl/6J mice to establish a high-fat diet (HFD)/CCl4 NASH model, with the aim of assessing the drug efficacy across low, medium, and high (0.3, 1, 3 mpk) dose groups administered twice a week for 28 days.Results
The animal pharmacological experiment of HSP763-01 demonstrated a significant reduction in body weight without apparent appetite suppression. Analysis of blood biochemic
SUBMITTER: Zhang Z
PROVIDER: S-EPMC12235361 | biostudies-literature | 2025 Apr
REPOSITORIES: biostudies-literature