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. 2018 Jun 22;12:1837–1853. doi: 10.2147/DDDT.S162950

Figure 3.

Figure 3

Figure 3

Salidroside inhibited ECM production and regulated the balance between MMP2 and TIMP1.

Notes: (A) Western blot and quantitative analyses. Salidroside decreased Col-1, α-SMA, and TIMP1 levels and increased MMP2 levels in the two liver fibrosis mouse models, compared with CCl4 or BDL treatment alone. (B) The qPCR analyses. Salidroside downregulated mRNA expression levels of Col-1α1, Col-1α2, α-SMA, and TIMP1 and upregulated MMP2 mRNA. (C) Immunohistochemical staining showed that the increased expression levels of Col-1 and α-SMA proteins in liver tissues in both CCl4 and BDL groups were ameliorated by salidroside (original magnification, ×200, scale bars =100 μm). Data were given as mean ± SD (n=8, *P<0.05 for CCl4 or BDL group vs vehicle or sham group, #P<0.05 for CCl4 + Sal 10 mg/kg or BDL + Sal 10 mg/kg vs CCl4 or BDL group, and +P<0.05 for CCl4 + Sal 20 mg/kg or BDL + Sal 20 mg/kg vs CCl4 + Sal 10 mg/kg or BDL + Sal 10 mg/kg).

Abbreviations: BDL, bile duct ligation; CCl4, carbon tetrachloride; ECM, extracellular matrix; qPCR, quantitative real-time polymerase chain reaction; Sal, salidroside; SD, standard deviation.