在人体血管组织中形成基酶依赖的血管新生素II
1Department of Pharmacology, Osaka Medical College, Takatsuki City, Osaka, Japan. Pha010@art.osaka-med.ac.jp
Circulation
|August 10, 1999
概括
肝素结合的人类化学酶对血管二酶的形成有显著的贡献,即使存在天然蛋白酶抑制剂,如α-抗素. 这凸显了它在体内 (in vivo) 的功能作用.
科学领域:
- 生物化学 生物化学
- 生理学 生理学 生理学
背景情况:
- 之前的研究表明,在蛋白酶抑制剂的存在下,人类心脏化学酶对血管素II形成的 in vitro 贡献有限.
- 基马酶活性的体内相关性,特别是当与肝素结合时,仍然不清楚.
研究的目的:
- 为了研究肝素结合的人类化学酶在血管素II形成中的作用.
- 评估天然蛋白酶抑制剂对这一过程的影响.
主要方法:
- 使用的人体血管组织提取物含有血管素I.
- 采用了氨酸亲和染色法来分离氨酸结合基酶.
- 评估 angiotensin II 的形成和通过lisinopril, chymostatin 和 alpha-antitrypsin 的抑制.
主要成果:
- 肝素结合的基马酶显示出显著的血管激素II形成活性.
- 这种活性被基莫斯塔丁和α-抗素抑制,表明它们的功能作用.
- ангиотензин II 的形成是时间依赖的,在肝素结合的部分中增强.
结论:
- 人类基马酶与肝素结合,在血管激素II的形成中起着至关重要的功能作用.
- 在存在自然蛋白酶抑制剂 (如α-antitrypsin) 的情况下,这种活性仍然存在.
- 研究结果表明,基马酶在体内生理性血管激素II生成中的重要性.
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