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源自牛奶酪蛋白的三肽异亮氨酸 - 脯氨酸 - 脯氨酸、缬氨酸 - 脯氨酸 - 脯氨酸和亮氨酸 - 脯氨酸对体外处理血管活性前体的酶的影响。

Effects of milk casein-derived tripeptides Ile-Pro-Pro, Val-Pro-Pro, and Leu-Pro-Pro on enzymes processing vasoactive precursors in vitro.

作者信息

Lehtinen Risto, Jauhiainen Tiina, Kankuri Esko, Lindstedt Ken, Kovanen Petri T, Kerojoki Outi, Korpela Riitta, Vapaatalo Heikki

机构信息

Institute of Biomedicine, Pharmacology, University of Helsinki, Finland.

出版信息

Arzneimittelforschung. 2010;60(4):182-5. doi: 10.1055/s-0031-1296270.

Abstract

Milk-based drinks containing casein-derived tripeptides isoleucine-proline-proline (Ile-Pro-Pro) and valine-proline-proline (Val-Pro-Pro) have been shown to possess antihypertensive and vascular endothelium-protecting properties in hypertensive animal models. Furthermore in clinical intervention trials they reduce blood pressure and arterial stiffness. The exact mechanisms are not known, but inhibition of angiotensin converting enzyme 1 (ACE1) has been suggested mainly to mediate these beneficial effects. The present study investigated the in vitro effects of three tripeptides: Ile-Pro-Pro, Val-Pro-Pro and leqcine-proline-proline (Leu-Pro-Pro) on four renin-angiotensin system enzymes: ACE1, ACE2, chymase, and cathepsin G. Also their effects on arginase I, a critical enzyme in L-arginine-nitric oxide pathway, were studied. It was shown, apparently for the first time, that the inhibitory effects of Ile-Pro-Pro, Val-Pro-Pro and Leu-Pro-Pro on ACE1 at micromolar concentrations are competitive in nature. Therefore the efficacy of inhibition is largely dependent on the amount of substrate present. Inhibition of ACE2 and arginase I was reached only at concentrations three orders of magnitude greater. No inhibition of chymase and cathepsin G was observed by the tripeptides. The findings support the hypothesis that Ile-Pro-Pro, Val-Pro-Pro and Leu-Pro-Pro act favourably on blood pressure mainly by selective inhibition of ACE1.

摘要

含有源自酪蛋白的三肽异亮氨酸 - 脯氨酸 - 脯氨酸(Ile - Pro - Pro)和缬氨酸 - 脯氨酸 - 脯氨酸(Val - Pro - Pro)的乳基饮料已被证明在高血压动物模型中具有降压和保护血管内皮的特性。此外,在临床干预试验中,它们可降低血压并减轻动脉僵硬程度。确切机制尚不清楚,但主要有人提出抑制血管紧张素转换酶1(ACE1)介导了这些有益作用。本研究调查了三种三肽:Ile - Pro - Pro、Val - Pro - Pro和亮氨酸 - 脯氨酸 - 脯氨酸(Leu - Pro - Pro)对四种肾素 - 血管紧张素系统酶:ACE1、ACE2、糜酶和组织蛋白酶G的体外作用。还研究了它们对精氨酸酶I(L - 精氨酸 - 一氧化氮途径中的关键酶)的影响。首次表明,Ile - Pro - Pro、Val - Pro - Pro和Leu - Pro - Pro在微摩尔浓度下对ACE1的抑制作用本质上是竞争性的。因此,抑制效果在很大程度上取决于底物的量。仅在浓度高三个数量级时才观察到对ACE2和精氨酸酶I的抑制。三肽未观察到对糜酶和组织蛋白酶G的抑制作用。这些发现支持了Ile - Pro - Pro、Val - Pro - Pro和Leu - Pro - Pro主要通过选择性抑制ACE1对血压产生有利作用的假说。

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