A selective ROCK inhibitor, Y27632, prevents dimethylnitrosamine-induced hepatic fibrosis in rats

Background: p160ROCK is a direct Rho target which mediates Rho-induced asse mbly of focal adhesions and stress fibers. We previously reported that Rho signaling pathways are involved in the activation of hepatic stellate cells (HSC) in vitro. The aim of the present study was to test the hypothesis th at an inhibitor specific for p160ROCK (Y27632) could prevent experimental h epatic fibrosis induced by dimethylnitrosamine (DMN) in rats. Methods: Y27632 was given orally at 30 mg/kg daily for 4 weeks after the fi rst injection of DMN. The degree of fibrosis was evaluated by image analysi s and also by measurements of collagen and hydroxyproline content in the li ver. The expression of alpha -smooth muscle actin (alpha -SMA) in the liver and in the primary cultured HSC was also evaluated. Semi-quantitative RT-P CR was performed to evaluate the expression of type I collagen mRNA in the liver. Results: Y27632 treatment significantly decreased the occurrence of DMN-ind uced hepatic fibrosis and reduced the collagen and hydroxyproline content a nd alpha -SMA expression in the liver. The expression of alpha -SMA in HSC was also suppressed in vitro. Conclusions: These findings indicate that inhibitors of the Rho-ROCK pathwa y might be useful therapeutically in hepatic fibrosis. (C) 2001 European As sociation for the Study of the Liver. Published by Elsevier Science B.V. Al l rights reserved.