血管紧张素受体–脑啡肽酶抑制剂LCZ696

被引:10
作者
刘巍
徐为人
汤立达
机构
[1] 天津药物研究院天津市新药设计与发现重点实验室
关键词
LCZ696; 血管紧张素受体–脑啡肽酶抑制剂; 心力衰竭; 高血压;
D O I
暂无
中图分类号
R972 [心血管系统药物];
学科分类号
100117 [系统生物医学];
摘要
脑啡肽酶属于一种中性肽链内切酶,其受到抑制可以提高利钠肽、缓激肽和P物质的生物活性,引起利尿、血管舒张和抗细胞增殖,进而产生明显的减轻心脏负荷和降低血压作用。LCZ696是诺华公司开发的第一个血管紧张素Ⅱ受体-脑啡肽酶双重抑制剂,由缬沙坦和sacubitril按物质的量1∶1共结晶组成,美国FDA于2014年7月已接受了它作为治疗射血分数降低心力衰竭(HFr EF)的新药申请。主要对LCZ696的基础药学、作用机制、药理作用以及临床治疗心力衰竭的有效性、安全性和耐受性等做一简述。
引用
收藏
页码:732 / 736
页数:5
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