Takai Shinji, Jin Denan
Department of Innovative Medicine, Graduate School of Medicine, Osaka Medical College, Takatsuki, Japan.
Department of Pharmacology, Osaka Medical College, Takatsuki, Japan.
Clin Exp Pharmacol Physiol. 2016 Apr;43(4):387-93. doi: 10.1111/1440-1681.12549.
Chymase has been identified as an angiotensin II-forming enzyme found in cardiovascular tissues. Angiotensin II is involved not only in the regulation of blood pressure, but also in the progression of cardiovascular remodelling. Interestingly, chymase inhibitors prevent cardiovascular remodelling without lowering blood pressure. The reason why chymase inhibitors do not affect blood pressure may depend on the localization of chymase in vivo. In normal tissues, chymase is stored in mast cell granules and has no enzymatic function; whereas, in damaged tissues, chymase exhibits enzymatic activity immediately following its release from the granules. Chymase also activates transforming growth factor-β and matrix metalloproteinase-9, both of which are involved in cardiovascular remodelling, and their enzymatic functions are also observed only in damaged tissues. In animal models of hypertension, diabetes and hypercholesterolaemia, chymase inhibitors improve cardiovascular remodelling without a general circulatory effect, including blood pressure. Thus, it is proposed that chymase is a potentially important target for preventing cardiovascular diseases.
糜酶已被确定为一种存在于心血管组织中的血管紧张素II生成酶。血管紧张素II不仅参与血压调节,还参与心血管重塑的进展。有趣的是,糜酶抑制剂可预防心血管重塑,而不会降低血压。糜酶抑制剂不影响血压的原因可能取决于其在体内的定位。在正常组织中,糜酶储存在肥大细胞颗粒中,没有酶活性;而在受损组织中,糜酶从颗粒中释放后立即表现出酶活性。糜酶还可激活转化生长因子-β和基质金属蛋白酶-9,二者均参与心血管重塑,且它们的酶活性也仅在受损组织中观察到。在高血压、糖尿病和高胆固醇血症的动物模型中,糜酶抑制剂可改善心血管重塑,而无包括血压在内的一般循环系统效应。因此,有人提出糜酶是预防心血管疾病的一个潜在重要靶点。