Data are the mean and standard deviation LY2835219 concentration relative transcript

level from 3 separate treatments on cells from the same donor, typical of at least 3 separate donors (c). Examination of myofibroblast expression of the major pro-fibrogenic cytokine TGFβ; the fibrogenic TIMP1 and collagen 1A1 mRNAs in human myofibroblasts treated with selected compounds showed that the PXR activator rifampicin (as previously reported [8]) and the PGRMC1 ligand GDC-0449 cost 4A3COOHmethyl inhibited the expression of all mRNAs, whereas other PGRMC1 ligands were less effective (Fig. 6c). Effect of administration of 4A3COOHmethyl in an animal model of liver fibrosis We selected 4A3COOHmethyl for use in an in vivo study for anti-fibrogenic activity, since this compound showed no activity as a PXR activator in either rat or human; competed with dexamethasone for binding to LAGS and was effective as a potential anti-fibrogenic in rat and human screens, in vitro. Since there was no information in the literature regarding any potential adverse effects of 4A3COOHmethyl administration, a pilot toxicity study was initially undertaken, in which adult male rats were administered 4A3COOHmethyl for 3 days at up to 100 mg/kg body weight by i.p. injection. Twenty four hours after the final treatment, liver

serum enzyme levels and liver pathology were examined and no adverse effects were observed (data not shown). To examine the effects of 4A3COOHmethyl on fibrosis, adult male rats were treated with 20 mg/kg body weight by i.p. injection every week

during an 8 week twice weekly treatment BMN 673 ic50 with CCl4, to generate liver fibrosis. A reduced dose of 20 mg/kg body weight was chosen because the compound was to be administered to rats with compromised liver function. Cediranib (AZD2171) To avoid potential interactions with CCl4, toxicity (i.e., reductions in CCl4 hepatotoxicity that could be misinterpreted as anti-fibrogenic effects), 4A3COOHmethyl was not administered within a 48 hour period of CCl4 administration. Previous work has established that a similar dose of PCN – using the same dosing regimen – is sufficient to modulate fibrosis in animal models of fibrosis [6]. Figure 7a indicates that 4A3COOHmethyl administration did not affect serum levels of ALT after 8 weeks confirming that 4A3COOHmethyl did not inhibit the toxicity of CCl4. However, immunohistochemical α-smooth muscle actin staining for liver myofibroblasts (data not shown), determination of collagen 1a1 mRNA levels (Fig. 7b) and a staining for scarring extracellular matrix protein (Fig. 7c and 7d) indicate that 4A3COOHmethyl also did not significantly affect fibrosis severity. Liver sections were therefore immunostained for the presence of rPGRMC1 in vivo using the IZAb. Figures 8a and 8b (high power) indicates that rPGRMC1 expression showed an enhanced centrilobular pattern of expression in hepatocytes with clear evidence of expression in non-parenchymal cells such as quiescent HSCs in control liver sections (Fig.