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. 2015 Jun;62(6):1398–1404. doi: 10.1016/j.jhep.2014.12.034

Fig. 1.

Fig. 1

UDCA alters key determinants of hepatic bile acid and cholesterol homeostasis. (A) mRNA analysis of bile acid biosynthesis markers. Controls: n = 18; UDCA: n = 19. (B) Representative Western blots of CYP7A1, FXR and densitometry (all samples) of protein levels relative to β-actin. Controls: n = 7; UDCA: n = 6. (C) ABCD-assay indicating FXR activity. Controls: n = 7; UDCA: n = 6. (D) mRNA analysis of cholesterol biosynthesis markers. Controls: n = 18; UDCA: n = 19. (E) Representative Western blots of HMGCR, phosphorylation status of HMGCR (HMGCRp), LDLR and densitometry (all samples). Controls: n = 7; UDCA: n = 6. Mean values ± SD are expressed for all data. p ⩽0.05, ∗∗p ⩽0.01 vs. control group.