Hematoxylin

and eosin (H&E) stainings of 3-μm paraffin sections were used to evaluate basic histomorphology of the specimens, especially the portal and lobular amount of inflammatory cells (score 0-3 for negative to strong infiltration) and signs of regeneration/degeneration of hepatocytes (e.g., cytoplasmic volume, nuclear polymorphism, and thickness of liver cell plates as well as hepatic apoptotic bodies).23 Content of extracellular collagen was measured by the amount of chromotrope-aniline blue (CAB) in the portal tract and hepatic lobule (score 0-3 for negative to strong staining).24 Proliferating selleck chemicals cell nuclear antigen (PCNA) and desmin staining were performed on an autostainer system (Dako), using the EnVision Detection System (Dako, Glostrup, Denmark), and developed using diaminobenzidine as the chromogen substrate (Roche Molecular Biochemicals, Mannheim, Germany), according to the manufacturer’s instructions. To highlight neutrophil granulocytes in liver tissue, naphtol AS-D chloroacetate esterase enzyme (NASD) histochemistry was used.25 Liver slices were stained for cluster of differentiation (CD)3 and forkhead box protein 3 (Foxp3) and developed with the PolapKit (Zytochem, Las Condes, Chile). Images were evaluated per mm2 (PCNA) or high-power field (400× magnification) using ImageAccess Enterprise software (version

9; Imagic, Glattbrugg, Switzerland). Histological quantification CYC202 manufacturer was performed by a pathologist. Results were analyzed using the Student’s t test, if two groups were compared; in addition, for analysis of real-time RT-PCR, logarithmized data and Welch’s t test were used. All data 上海皓元医药股份有限公司 in this study are expressed as a mean ± standard error of the mean. P ≤ 0.05 was considered significant. HO-1 induction or overexpression have been shown to interfere with liver damage in mouse models of acute inflammation and apoptosis.7, 8 We have investigated the effects of HO-1 induction on chronic hepatic inflammation and fibrosis in Mdr2ko mice. Nine weeks of HO-1 induction in Mdr2ko mice (weeks 5-14 of lifespan) decreased plasma ALT levels, which increased over the first 22 weeks of lifespan (Fig. 1A, open bars). Significant

improvement was observed for at least 8 weeks beyond treatment (Fig. 1A, closed bars). HO-1 induction by CoPP in liver tissue was detectable on messenger RNA (mRNA) (Supporting Fig. 1A) and protein level (Supporting Fig. 1B) and did not alter hematocrit values (Supporting Fig. 1C). Likewise, isolated PHs and HSCs of Mdr2ko mice showed HO-1 induction after CoPP incubation (Supporting Fig. 1D). IHC staining of liver samples obtained at 12 weeks of age revealed reduced periportal and lobular inflammation in CoPP-treated mice (Fig. 1B). HO-1 induction significantly reduced the expression of TNFR1 and 2, whereas TNF expression in whole liver tissue was increased in Mdr2ko mice, compared to FVB background control (data not shown), but was not altered by HO-1 induction (Fig. 1C).