Basic Research
Copyright ©2008 The WJG Press and Baishideng.
World J Gastroenterol. Jul 21, 2008; 14(27): 4324-4331
Published online Jul 21, 2008. doi: 10.3748/wjg.14.4324
Figure 1
Figure 1 Time course of effects on the IGF-I system, JNK1/2 activity, and cell viability induced by ethanol in primary cultured rat hepatocytes (mean ± SD). The cells were exposed to 200 mmol/L ethanol for 0, 60, 120 and 180 min. A: P-JNK1/2, t-JNK1/2, and IGF-IR activities; B: IGF-I concentration; C and D: IGF-I mRNA expression; E: Cell viability. β-actin (A) and GAPDH (C) were used as loading controls. The mRNA expression (as indicated by a band at 180 bp, C) was determined by densitometric analysis (D) of the amplification products. Data represent percentages relative to control. The cell viability (D) was determined by the MTT assay. aP < 0.05, bP < 0.01 vs control (n = 6).