摘要
替米沙坦是一种非肽类血管紧张素Ⅱ受体拮抗剂,可选择性、难以逆转的阻滞AT1受体,而对其他受体,尤其是心血管系统的受体无影响。与安慰剂相比,给予Ⅰ-Ⅱ期高血压患者40—160mg/次,qd给药时,可显著降低收缩压和舒张压,其疗效至少与阿替洛尔50,100mg或赖诺普利10-40mg相当。本品耐受性良好。
Telmisartan, a nonpeptide angiotensin Ⅱ receptor antagonist, selectively and unconvertiblely inhibits AT1 receptor without action on other receptors especially those in cardiovascular system. Its efficacy, tolerability, and clinical uses were reviewed.
出处
《中国新药杂志》
CAS
CSCD
1999年第12期801-802,共2页
Chinese Journal of New Drugs