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©The Author(s) 2018.
World J Gastroenterol. Mar 7, 2018; 24(9): 992-1003
Published online Mar 7, 2018. doi: 10.3748/wjg.v24.i9.992
Published online Mar 7, 2018. doi: 10.3748/wjg.v24.i9.992
Figure 2 PI3K-AKT-mTOR pathway was involved in autophagy in Jiang Zhi Granule-treated cells.
A: HepG2 cells were treated with 0.4 mmol/L PA and rapamycin (2 μmol/L) or JZG (100 μg/mL) for 24 h; B: HepG2 cells were treated with 0.4 mmol/L PA and rapamycin (2 μmol/L) or JZG (100 μg/mL) for 48 h; C: HepG2 cells stably expressing mRFP-GFP-LC3 were pretreated with 0.4 mmol/L PA and rapamycin (2 μmol/L) or JZG (100 μg/mL) for 24 h and 48 h, and then analyzed by fluorescence microscopy. Data are expressed as mean ± SEM. aP < 0.05, bP < 0.01, eP < 0.001. JZG: Jiang Zhi Granule; PA: Palmitate.
- Citation: Zheng YY, Wang M, Shu XB, Zheng PY, Ji G. Autophagy activation by Jiang Zhi Granule protects against metabolic stress-induced hepatocyte injury. World J Gastroenterol 2018; 24(9): 992-1003
- URL: https://www.wjgnet.com/1007-9327/full/v24/i9/992.htm
- DOI: https://dx.doi.org/10.3748/wjg.v24.i9.992