Figures & data
Table I. Gene-specific primers for the lipid metabolism enzyme of mRNAs.
Table II. Effect of 3-d DEX treatment (DEX, 2 mg/kg BM) on BM gain (n = 3), feed intake (n = 3), and organ index (% of BM, n = 8) of broiler chickens.
Table III. Effect of 3-d DEX treatment (DEX, 2 mg/kg BM) on plasma metabolite and insulin concentrations of broiler chickens in fasting and fed states.
Figure 1. Effects of 3-d DEX treatment (DEX, 2 mg/kg BM) on the hepatic expression of mRNAs for ACC, FAS, and ME in broiler chickens in fasting (A) and fed states (B) Values were determined in duplicate for each sample; values are means ± SEM (n = 8); a–bmeans with different letters differ significantly, P < 0.05, by ANOVA.
![Figure 1. Effects of 3-d DEX treatment (DEX, 2 mg/kg BM) on the hepatic expression of mRNAs for ACC, FAS, and ME in broiler chickens in fasting (A) and fed states (B) Values were determined in duplicate for each sample; values are means ± SEM (n = 8); a–bmeans with different letters differ significantly, P < 0.05, by ANOVA.](/cms/asset/fe2a3105-df7d-4c80-898d-5401473c63e8/ists_a_543444_f0001_b.gif)
Figure 2. Effects of DEX and insulin treatment on the expression of mRNAs for ACC, FAS, ME, LXR, and SREBP-1 in hepatocytes cultured in vitro. Values were determined in duplicate for each sample; values are means ± SEM (n = 8); a–bmeans with different letters differ significantly, P < 0.05, by ANOVA.
![Figure 2. Effects of DEX and insulin treatment on the expression of mRNAs for ACC, FAS, ME, LXR, and SREBP-1 in hepatocytes cultured in vitro. Values were determined in duplicate for each sample; values are means ± SEM (n = 8); a–bmeans with different letters differ significantly, P < 0.05, by ANOVA.](/cms/asset/474e433a-9b1c-45a4-97af-f17feb452a09/ists_a_543444_f0002_b.gif)