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Updated: May 1, 2026

Mouse Model of Metabolic Dysfunction-Associated Steatotic Liver Disease with Fibrosis
Published on: July 18, 2025
[Therapeutic effect of fibroblast growth factor 21 on NAFLD in MSG-iR mice and its mechanism]
Abstract:
This study is to evaluate the therapeutic effect of fibroblast growth factor 21 (FGF21) on NAFLD in MSG-IR mice and to provide mechanism insights into its therapeutic effect. The MSG-IR mice with insulin resistance were treated with high dose (0.1 micromol.kg-1d-1) and low dose (0.025 micromol.kg-1d-1) of FGF21 once a day for 5 weeks. Body weight was measured weekly. At the end of the experiment, serum lipids, insulin and aminotransferases were measured. Hepatic steatosis was observed. The expression of key genes regulating energy metabolism were detected by real-time PCR. The results showed that after 5 weeks treatment, both doses of FGF21 reduced body weight (P<0.01), corrected dyslipidemia (P<0.01), reversed steatosis and restored the liver morphology in the MSG model mice and significantly ameliorated insulin resistance. Additionally, real-time PCR showed that FGF21 significantly reduced transcription levels of fat synthetic genes, decreased fat synthesis and promoted lipolysis and energy metabolism by up-regulating key genes of lipolysis, thereby liver fat accumulation was reduced and liver function was restored to normal levels. In conclusion, FGF21 significantly reduces body weight of the MSG-IR mice, ameliorates insulin resistance, reverses hepatic steatosis. These findings provide a theoretical support for clinical application of FGF21 as a novel therapeutics for treatment of NAFLD.
Insights
Fibroblast growth factor 21 (FGF21) effectively treats non-alcoholic fatty liver disease (NAFLD) by reducing body weight, improving insulin resistance, and reversing liver steatosis in mice. This study supports FGF21 as a potential therapeutic for NAFLD.
Area of Science:
- Metabolic disease research
- Hepatology
- Endocrinology
Background:
- Non-alcoholic fatty liver disease (NAFLD) is a growing health concern.
- Insulin resistance is a key factor in NAFLD development.
- Fibroblast growth factor 21 (FGF21) is being investigated for metabolic benefits.
Purpose of the Study:
- To evaluate the therapeutic efficacy of FGF21 in a mouse model of NAFLD with insulin resistance (MSG-IR mice).
- To elucidate the underlying mechanisms of FGF21's action on NAFLD.
- To assess FGF21's impact on body weight, insulin sensitivity, and liver health.
Main Methods:
- MSG-IR mice were treated with high or low doses of FGF21 daily for 5 weeks.
- Body weight, serum lipids, insulin, and aminotransferases were measured.
- Hepatic steatosis was assessed, and gene expression related to energy metabolism was analyzed via real-time PCR.
Main Results:
- FGF21 treatment significantly reduced body weight and corrected dyslipidemia in MSG-IR mice.
- Hepatosteatosis was reversed, liver morphology was restored, and insulin resistance was ameliorated.
- FGF21 downregulated fat synthesis genes and upregulated lipolysis genes, reducing liver fat accumulation.
Conclusions:
- FGF21 demonstrates significant therapeutic potential for NAFLD by improving metabolic parameters and liver function.
- The study provides mechanistic insights into FGF21's role in reducing hepatic fat accumulation.
- These findings support the clinical investigation of FGF21 as a novel treatment for NAFLD.
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