Kim Young-Jin, Uyama Hiroshi, Kobayashi Shiro
Department of Materials Chemistry, Graduate School of Engineering, Kyoto University, Kyoto 615-8510, Japan.
Biochem Biophys Res Commun. 2004 Jul 16;320(1):256-61. doi: 10.1016/j.bbrc.2004.05.163.
Inhibition effects of (+)-catechin-aldehyde polycondensates against the activity of proteinases, Clostridium histolyticum collagenase (ChC) and human neutrophil elastase (HNE) causing proteolytic degradation of extracellular matrix (ECM), have been investigated. In normal tissues, a balance is reached between the formation and destruction of ECM, leading to a state of homeostasis. However, uncontrolled destruction of ECM contributes to tumor invasion and metastasis. In the measurement of the inhibition activity on ChC and HNE, the polycondensates exhibited superior effects compared to the catechin monomer. Kinetic assays of ChC and HNE inhibition by the polycondensate clearly showed a mixed-type inhibition. These data demonstrate that the polycondensates are a new class of proteinase inhibitors useful for a potent therapeutic agent.
研究了(+)-儿茶素醛缩聚物对导致细胞外基质(ECM)蛋白水解降解的蛋白酶、溶组织梭菌胶原酶(ChC)和人中性粒细胞弹性蛋白酶(HNE)活性的抑制作用。在正常组织中,ECM的形成与破坏之间达到平衡,导致内稳态状态。然而,ECM的不受控制的破坏会促进肿瘤侵袭和转移。在对ChC和HNE的抑制活性测量中,缩聚物表现出比儿茶素单体更优异的效果。缩聚物对ChC和HNE抑制的动力学测定清楚地显示出混合型抑制。这些数据表明,缩聚物是一类新型的蛋白酶抑制剂,可作为一种有效的治疗剂。