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Updated: Oct 11, 2025

Measuring the Rate of Lipolysis in Ex Vivo Murine Adipose Tissue and Primary Preadipocytes Differentiated In Vitro
Published on: March 17, 2023
Chlorogenic Acids Inhibit Adipogenesis: Implications of Wnt/β-Catenin Signaling Pathway
Mengting Liu1, Jian Qin2, Jing Cong3
1The First Affiliated Hospital of Guangdong Pharmaceutical University, Guangzhou 510080, China.
Abstract:
In our previous in vitro study, we found that chlorogenic acid (CGA) inhibited adipocyte differentiation and triglyceride (TG) accumulation, but the underlying mechanism is still unclear. Accumulative genetic evidence supports that canonical Wnt signaling is a key modulator on adipogenesis. Methods. In this study, 3T3-L1 cells were induced adipogenic differentiation and then treated with CGA. We investigate the effect of CGA in inhibiting adipogenesis and evaluate its role in modulating Wnt10b (wingless integration1 10b), β-catenin, glycogen synthase kinase-3β (GSK-3β), and peroxisome proliferator-activated receptor γ (PPAR-γ) involved in the Wnt (wingless integration1)/β-catenin signaling pathway. Results. The result showed that after CGA treatment, lipid accumulation and TG level decreased significantly in 3T3-L1 cells, indicating that CGA could inhibit adipogenesis. In addition, CGA repressed the induction of adipocyte differentiation biomarkers as PPAR-γ, adipocyte protein 2 (aP2), fatty acid synthase (FAS), and lipoprotein lipase (LPL), and the secretion of GSK-3β in a dose-dependent manner upregulated the expression of β-catenin and Wnt10b both in gene and protein levels. Moreover, CGA induced phosphorylation of GSK-3β and promoted the accumulation of free cytosolic β-catenin in 3T3-L1 adipocytes. Conclusion. Overall, these findings gave us the implications that CGA inhibits adipogenesis via the canonical Wnt signaling pathway.
Insights
Chlorogenic acid (CGA) inhibits fat cell (adipocyte) formation and fat (triglyceride) buildup by activating the Wnt signaling pathway, offering a potential strategy for managing obesity.
Area of Science:
- Biochemistry
- Molecular Biology
- Cell Biology
Background:
- Adipogenesis, the process of fat cell differentiation, is a complex mechanism regulated by various signaling pathways.
- The canonical Wnt signaling pathway plays a crucial role in modulating adipogenesis.
- Chlorogenic acid (CGA) has shown potential in inhibiting adipocyte differentiation and triglyceride accumulation, but its mechanism remains unclear.
Purpose of the Study:
- To investigate the mechanism by which CGA inhibits adipogenesis.
- To evaluate the effect of CGA on the Wnt/β-catenin signaling pathway.
- To assess CGA's impact on key adipogenic markers and Wnt pathway components.
Main Methods:
- 3T3-L1 cells were induced for adipogenic differentiation and subsequently treated with CGA.
- The expression and levels of Wnt10b, β-catenin, GSK-3β, and PPAR-γ were analyzed.
- Adipogenic biomarkers (PPAR-γ, aP2, FAS, LPL) and triglyceride accumulation were quantified.
Main Results:
- CGA significantly reduced lipid accumulation and triglyceride levels in 3T3-L1 cells.
- CGA repressed the expression of adipogenic differentiation markers.
- CGA upregulated Wnt10b and β-catenin expression while increasing GSK-3β phosphorylation and β-catenin accumulation.
Conclusions:
- Chlorogenic acid effectively inhibits adipogenesis in 3T3-L1 cells.
- CGA exerts its anti-adipogenic effects by modulating the canonical Wnt signaling pathway.
- These findings suggest CGA as a potential therapeutic agent for obesity management.
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