Histopathological changes were evaluated by hematoxylin and eosin

Histopathological changes were evaluated by hematoxylin and eosin staining and by Masson’s trichrome method. PI3K and actin expression in the livers were determined by Western blot. FRNK plasmid was used to transfect HSCs. HSC adhesion was

examined by toluidine blue colorimetric assay. HSC migration was evaluated by improved Boyden double-chamber. PI3K expression in HSCs was determined by RT-PCR and Western blot. AP-1 (c-fos, c-jun) mRNA in HSCs was selleck chemicals llc assessed by RT-PCR. Results: Hematoxylin and eosin staining of liver established the bile duct ligated rats. The data suggests that actin and PI3K expression in liver of the bile duct ligated rats was increased following the changes of hepatic fibrosis. At the same time, c-fos and c-jun mRNA in the livers was increased. Overexpression of FRNK can inhibit HSC adhesion and migration time-dependently. Simultaneously FRNK inhibited the PI3K mRNA and protein expression c-jun mRNA expression. Conclusion: FRNK inhibited HSC adhesion and migration by decreasing the expressions of FAK-PI3K-AP-1 signal pathway. Key Word(s): 1. HSC; 2. FRNK; 3. PI3K; 4. AP-1; Presenting Author: QI ZHOU Additional Authors: JUAN YANG, NANNAN XU, MIN WANG, LAI WEI Corresponding Author: JUAN YANG, QI ZHOU Affiliations: Tongji Medical College; Tongji Medical College Objective: In cirrhosis, the up-regulation selleckchem of RhoA/Rho-kinase signaling pathway leads to portal

hypertension by promoting constriction of vascular smooth muscle, inhibiting eNOS (endothelial nitric oxide synthase) synthesis and against hepatic stellate cell

(HSC) apoptosis. Sodium ferulate (SF) is effective in lowering cholesterol synthesis, and geranylgeranyl-pyrophosphate (GGPP), the intermediate product of cholesterol synthesis, contributes to RhoA activation. We were aim at investigating the effect of SF in cirrhotic rats and isolated HSC. Methods: Cirrhosis of rats was induced by bile duct ligation. Three weeks later, they were treated by SF or normal saline for one week separately. Sham-operated rats were set as controls. Cytidine deaminase Compare biochemical parameters between groups. Hepatic hydroxyproline content, pathological characteristics of liver sections, and hepatic α-SMA detected by immunohistochemistry were analyzed to assess fibrosis degree. Hepatic RhoA, Rho-kinase and eNOS were studied by immunohistochemistry. Flow cytometry was performed to compare apoptosis rate between SF-treated and SF + GGPP treated HSC (both isolated rat HSC and LX-2). Intrahepatic resistance and responsiveness of methoxamine between groups were investigated by in situ liver perfusion. Results: Hepatic biochemical parameters and hydroxyproline content did not differ between SF-treated or untreated cirrhotic rats. Pathological observation revealed that, the hepatocyte damage and fibrosis degree were lower in cirrhotic rats treated by SF. In cirrhosis, after treated by SF, the expression of α-SMA and Rho-kinase decreased, reversely eNOS increased.

Comments are closed.