Inhibitory Activity of Drynariae rhizoma Extracts on Cathepsin Having Bone Resorption Activity

Abstract

Effects of traditional Korean (Hanbang) medicine, Drynariae rhizoma (DR), on the protease activity of bone loss‐initiation in rats and mice were investigated. Ethanol extracts‐DR (EE‐DR) and water extracts‐DR (WE‐DR) were identified as potent inhibitor of cathepsins K and L. The original WE‐DR inhibits cathepsins K and L with IC50 values of 3.7 µg/ml and 4.5 µg/ml, respectively. EE‐DR was more potent than that of WE‐DR, because the inhibitions of cathepsin K and L increased to 0.5 µg/ml and 0.8 µg/ml, respectively. The EE‐DR was proved to be the most potent. EE‐DR was found to be a potent inhibitor of cathepsins K with a Ki value of 5.0 µg/ml for cathepsin K. The activity was increased by 10‐fold when the assay is performed in the presence of glutathione at pH 7.0, which favors the formation of a GSH thiolate anion. Thus, it is suggested that this increase in potency is probably due to an enhanced chemical reactivity of the extract mixtures toward the thiolate of the active site of the enzyme. WE‐DR exhibited time‐dependet inhibition which allowed us to determine the association and dissociation rate constants with cathepsin K. Finally, EE‐DR inhibits bone resorption in an in vitro assay involving mouse osteoclasts and bovine bone with an IC50 value of 70 µg/ml. WE‐DR represents a new herbal formulation inhibiting cathepsin K and L activity and proteolysis of bone collagen. These results strongly suggest that DR is effective for preventing the development of bone loss induced by cathepsin K. This result also suggested that the DR is effective for bone resorptive action in bone cells.