Effects of daphnodorin A, daphnodorin B and daphnodorin C on human chymase-dependent angiotensin II formation

被引:26
|
作者
Takai, S [1 ]
Sakaguchi, M
Jin, DN
Baba, K
Miyazaki, M
机构
[1] Osaka Med Coll, Dept Pharmacol, Takatsuki, Osaka 5698686, Japan
[2] Osaka Univ Pharmaceut Sci, Dept Pharmacognosy, Takatsuki, Osaka 5691041, Japan
关键词
angiotensin II; chymase; angiotensin converting enzyme; human; human chymase inhibitor;
D O I
10.1016/S0024-3205(99)00135-6
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
We investigated whether daphnodorin A, daphnodorin B and daphnodorin C inhibited human chymase-dependent angiotensin II-forming activity. Although the structures of these compounds are very similar, daphnodorin A completely inhibited angiotensin II formation generated by chymase, while daphnodorin B partially inhibited and daphnodorin C did not. On the other hand, these daphnodorins did not affect angiotensin converting enzyme-dependent angiotensin II formation. Furthermore, these daphnodorins did not inhibit purified human tryptase, which, like chymase, is contained in mast cells. Therefore, daphnodorin A, but not daphnodorin B and daphnodorin C, may specifically inhibit the chymase-dependent angiotensin II formation, and such differences between inhibitory effects of these compounds to human chymase may be useful for the development of human chymase inhibitor.
引用
收藏
页码:1889 / 1896
页数:8
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