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©2012 Baishideng Publishing Group Co.
World J Gastroenterol. Oct 28, 2012; 18(40): 5709-5718
Published online Oct 28, 2012. doi: 10.3748/wjg.v18.i40.5709
Published online Oct 28, 2012. doi: 10.3748/wjg.v18.i40.5709
Figure 3 Effect of ethyl pyruvate on high mobility group box-1 expression in liver tissues of rat acute-on-chronic liver failure model.
A: A representative reverse transcription-polymerase chain reaction specific for high mobility group box-1 (HMGB1) mRNA and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mRNA (internal control) in each group shown in the electrophotogram; B: Western blot assay showing the expression of HMGB1 protein in the liver tissues of rats in each group. bP < 0.01 vs normal; cP < 0.05 vs model; eP < 0.05 vs ethyl pyruvate (EP) treatment at 3 h. The time points of 3 h, 6 h, 12 h and 24 h represent four subgroups of EP treatment group. Results are expressed as mean ± SD (n = 5). N: Normal group; M: Model group.
- Citation: Wang LW, Wang LK, Chen H, Fan C, Li X, He CM, Gong ZJ. Ethyl pyruvate protects against experimental acute-on-chronic liver failure in rats. World J Gastroenterol 2012; 18(40): 5709-5718
- URL: https://www.wjgnet.com/1007-9327/full/v18/i40/5709.htm
- DOI: https://dx.doi.org/10.3748/wjg.v18.i40.5709