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©2006 Baishideng Publishing Group Co.
World J Gastroenterol. Jan 14, 2006; 12(2): 214-221
Published online Jan 14, 2006. doi: 10.3748/wjg.v12.i2.214
Published online Jan 14, 2006. doi: 10.3748/wjg.v12.i2.214
Figure 5 Effects of PGG-induced ERK activation on HO-1 expression and t-Bt-HP-induced toxicity in HepG2 cells.
A: Cells were incubated with 20 µmol/L PGG for indicated times, and Western blotting was performed with specific antibodies; B: Cells were incubated with 20 µmol/L PGG for 12 h in the presence or absence of 10 µmol/L U0123 (UO), 20 µmol/L SB203580 (SB), or 20 µmol/L SP600125 (SP), and Western blotting was performed with HO-1 antibody; C: Cells untreated or treated with PGG in the presence or absence of each specific inhibitor for 12 h were exposed to 100 µmol/L t-Bt-HP for 4 h. Data are expressed as mean ± SE of five independent experiments.
- Citation: Pae HO, Oh GS, Jeong SO, Jeong GS, Lee BS, Choi BM, Lee HS, Chung HT. 1,2,3,4,6-penta-O-galloyl-β-D-glucose up-regulates heme oxygenase-1 expression by stimulating Nrf2 nuclear translocation in an extracellular signal-regulated kinase-dependent manner in HepG2 cells. World J Gastroenterol 2006; 12(2): 214-221
- URL: https://www.wjgnet.com/1007-9327/full/v12/i2/214.htm
- DOI: https://dx.doi.org/10.3748/wjg.v12.i2.214