©The Author(s) 2025.
World J Hepatol. Dec 27, 2025; 17(12): 113660
Published online Dec 27, 2025. doi: 10.4254/wjh.v17.i12.113660
Published online Dec 27, 2025. doi: 10.4254/wjh.v17.i12.113660
Figure 7 Xietu Hemu prescription inhibits lipid synthesis of mature 3T3-L1 cells through the leptin signal axis at the protein level of the nucleus and cytoplasm.
A: Secretion levels of leptin (LEP) at different time points during high dose of Xietu Hemu prescription (XHP) intervention in 3T3-L1 cell differentiation; B: Immunofluorescence assay for protein expression of LEP after 10 days of XHP intervention in 3T3-L1 cell differentiation at different concentrations; C-H: Detection and quantitative statistics of cytoplasm protein levels on day 10 (n = 3); I-K: Detection and quantitative statistics of nucleus protein levels on day 10 (n = 3). Data were expressed as mean ± SEM. 200 ×, 50 μm; 400 ×, 25 μm; aP < 0.05 vs control; bP < 0.01 vs control; cP < 0.005 vs control; dP < 0.001 vs control; eP < 0.05 vs model; fP < 0.01 vs model; gP < 0.005 vs model; hP < 0.001 vs model; iP < 0.05 vs low dose of XHP (L-XHP); jP < 0.001 vs L-XHP; kP < 0.001 vs medium dose of XHP. L-XHP: Low dose of Xietu Hemu prescription; M-XHP: Medium dose of Xietu Hemu prescription; H-XHP: High dose of Xietu Hemu prescription; LEP: Leptin.
- Citation: Cheng Z, Lu YF, He YX, Wei W, Xie YX, Lv TS, Wei Y, Lou Y, Yu JY, Zhou XQ. Integrated serum metabolomics reveal molecular mechanism of Xietu Hemu prescription on metabolic dysfunction-associated steatotic liver disease-related obesity. World J Hepatol 2025; 17(12): 113660
- URL: https://www.wjgnet.com/1948-5182/full/v17/i12/113660.htm
- DOI: https://dx.doi.org/10.4254/wjh.v17.i12.113660