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. 2022 Feb 25;2022:7781910. doi: 10.1155/2022/7781910

Figure 6.

Figure 6

RES suppressed the HG‐induced activation of pathways of TGF‐β1/Smad3 and NF-κB dependent on RAGE in vitro. H9c2 cells were treated with control medium or indicated concentration of RES (40 μg/mL) or FPS-ZM1 (100 μM) for 24 h. WB analysis of RAGE, p-NF-κB P65, P65, TGF‐β1, p-Smad3, Smad3, and GAPDH levels was performed. (a, d) Representative WB images of RAGE, p-NF-κB P65, P65, TGF‐β1, p-Smad3, Smad3, and GAPDH levels; (b) protein expression of RAGE, (c) p-NF-κB P65, (e) TGF‐β1, and (f) p-Smad3. The levels of protein were determined by densitometry and normalised to the levels of GAPDH. The data are presented as the means ± SD of the three repeated experiments; p < 0.05 vs, HG group.