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人类中依赖糜蛋白酶的血管紧张素II形成系统。

Chymase-dependent angiotensin II forming systems in humans.

作者信息

Urata H, Nishimura H, Ganten D

机构信息

Max-Delbrück-Centrum for Molecular Medicine, Department of Hypertension Research, Berlin-Buch, Germany.

出版信息

Am J Hypertens. 1996 Mar;9(3):277-84. doi: 10.1016/0895-7061(95)00349-5.

Abstract

Recent studies have provided evidence that human cardiovascular tissues contain components of the renin angiotensin system: angiotensinogen, renin, angiotensin I converting enzyme (ACE), chymase, and angiotensin (Ang) II receptors. It is likely that locally produced Ang II plays an important role in cardiovascular homeostasis in autocrine and paracrine fashions and may also be involved in remodeling of the heart and vasculature in pathological conditions. In addition to ACE, a cardiac Ang II-forming serine proteinase (human heart chymase) has been identified in the left ventricle of the human heart. The different cellular and regional distribution of ACE and heart chymase in the heart as well as in blood vessels implies distinct pathophysiological roles of these two Ang II-forming enzymes. Several reports indicate that both ACE dependent and ACE independent Ang II formation appears to take place in hypoxic or ischemic heart or blood vessel in vivo and seems to be involved in their pathological changes. However, chymase dependent Ang II formation, chymostatin sensitive but aprotinin insensitive, does not explain all of ACE independent Ang II formation. Therefore, it has become quite important to clarify the detailed mechanisms of the tissue Ang II formation in humans and their contribution to the pathophysiological changes in cardiovascular diseases.

摘要

最近的研究提供了证据,表明人类心血管组织含有肾素血管紧张素系统的成分:血管紧张素原、肾素、血管紧张素I转换酶(ACE)、糜酶和血管紧张素(Ang)II受体。局部产生的Ang II可能以自分泌和旁分泌方式在心血管稳态中发挥重要作用,并且在病理状态下也可能参与心脏和血管的重塑。除了ACE之外,在人类心脏的左心室中已鉴定出一种形成心脏Ang II的丝氨酸蛋白酶(人心脏糜酶)。ACE和心脏糜酶在心脏以及血管中的不同细胞和区域分布意味着这两种形成Ang II的酶具有不同的病理生理作用。几份报告表明,依赖ACE和不依赖ACE的Ang II形成似乎都在体内缺氧或缺血的心脏或血管中发生,并且似乎参与了它们的病理变化。然而,依赖糜酶的Ang II形成,对糜蛋白酶抑制剂敏感但对抑肽酶不敏感,无法解释所有不依赖ACE的Ang II形成。因此,阐明人类组织中Ang II形成的详细机制及其对心血管疾病病理生理变化的作用变得非常重要。

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