Tetrandrine, one of the alkaloids isolated from the Chinese herb Radix stephania tetrandra S Moore, has traditionally been used to treat hypertension and silicosis. It has also been shown to exhibit antifibrogenic activity against fibroblasts, particularly pulmonary fibroblasts (Reist et al. 1993), strong binding to alveolar macrophages (Ma et al. 1991), inhibition of proliferative activity of pulmonary fibroblast, and an inhibitory effect on types I and III collagen gene mRNA level in lung tissue of rats (Liu et al. 1994).We have previously reported that tetrandrine has an antifibrotic effect on liver fibrosis in rats induced by bile duct ligation and scission and tetrandrine exert a direct inhibition effect on rat hepatic stellate cell activation (Park et al. 2000).Previous studies suggest that collagenase activity becomes deficient during evolution of liver fibrosis in animal models and in humans (Takahashi et al. 1980;Maruyama et al. 1982;Rerez-Tamayo et al. 1987), and the studied described earlier suggest that this may be caused by the tissue inhibitor of metalloproteinase overexpression. Continued inhibition of extracellular matrix degradation by the tissue inhibitor of metalloproteinases may block the ability to recover from fibrosis, even after removal of the injury. These data suggest that the tissue inhibitor of metalloproteinases play a predominant role in regulating fibrosis by protecting fibrotic extracellular matrix from degradation by collagenase and possibly other metalloproteinases.Therefore, the purpose of the present study was to clarify the effects of a tetrandrine on tissue inhibitor of metalloproteinase-1 and collagen type I were examined in rat fibrotic liver induced by bile duct ligation and scission.Males Sprague-Dawley rats (initial body weight 220-250 g) were used. Rats were anaesthetized with ketamine/rompun and double ligatures were performed on the common