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Therapeutic Perspectives of Angiotensin-(1-7) in the Treatment ofCardiovascular Disease

机译:血管紧张素-(1-7)在心血管疾病治疗中的治疗前景

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In the last decade, new biologically active components of the renin-angiotensin system were found. Angiotensin-(1-7)(Ang-(1-7)), a metabolite of angiotensin I and angiotensin II (Ang II), is considered the most pleiotropiccomponent of the renin-angiotensin system, acting as a counterregulatory mediator of Ang II. Ang-(1-7) exerts beneficialeffects on the cardiovascular system, including reduction of blood pressure, myocardial antihypertrofic and antifibrotic actions,and reversal of renal dysfunction, among others. Recent discovery of enzymatic pathways involved in Ang-(1-7)synthesis, such as the angiotensin-converting enzyme-2 (ACE2) and the existence of a specific receptor to this heptapeptide,the Mas receptor, have increased interest in the design of therapeutic strategies aimed at increasing the biological actionsof Ang-(1-7). ACE inhibitors, AT1 receptor blockers and aldosterone antagonists enhance Ang-(1-7) levels by differentmechanisms. Actually, non-peptidic Ang-(1-7) agonists and ACE2 activators are under development and couldhave a role in the treatment of cardiovascular diseases. The aim of the present review is to describe the biochemical and physiological actions of Ang-(1-7), the therapeuticstrategies designed to enhance Ang-(1-7) activity foccusing in their possible role and limitations in the treatment of cardiovasculardisease.
机译:在最近的十年中,发现了肾素-血管紧张素系统的新的生物活性成分。血管紧张素I和血管紧张素II(Ang II)的代谢产物血管紧张素-(1-7)(Ang-(1-7))被认为是肾素-血管紧张素系统的最强活性成分,可作为Ang II的反调节介体。 Ang-(1-7)对心血管系统产生有益的影响,包括降低血压,降低心肌的抗高血压和抗纤维化作用以及逆转肾功能不全等。最近发现了与Ang-(1-7)合成有关的酶促途径,例如血管紧张素转化酶2(ACE2)以及该七肽的特异性受体Mas受体的存在,引起了人们对Ang-(1-7)合成的兴趣的增加。旨在提高Ang-(1-7)生物学活性的治疗策略。 ACE抑制剂,AT1受体阻滞剂和醛固酮拮抗剂通过不同机制提高Ang-(1-7)水平。实际上,非肽Ang-(1-7)激动剂和ACE2激活剂正在开发中,并可能在心血管疾病的治疗中发挥作用。本综述的目的是描述Ang-(1-7)的生化和生理作用,旨在增强Ang-(1-7)活性的治疗策略主要是由于其在心血管疾病中的可能作用和局限性。

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