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ACE2/Ang-(1–7) signaling and vascular remodeling

机译:ACE2 / Ang-(1-7)信号传导和血管重塑

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The renin-angiotensin system (RAS) regulates vascular tone and plays a critical role in vascular remodeling, which is the result of a complex interplay of alterations in vascular tone and structure. Inhibition of the RAS has led to important pharmacological tools to prevent and treat vascular diseases such as hypertension, diabetic vasculopathy and atherosclerosis. Angiotensin converting enzyme 2 (ACE2) was recently identified as a multifunctional monocarboxypeptidase responsible for the conversion of angiotensin (Ang) II to Ang-(1–7). The ACE2/Ang-(1–7) signaling has been shown to prevent cellular proliferation, pathological hypertrophy, oxidative stress and vascular fibrosis. Thus, the ACE2/Ang-(1–7) signaling is deemed to be beneficial to the cardiovascular system as a negative regulator of the RAS. The addition of the ACE2/Ang-(1–7) signaling to the complexities of the RAS may lead to the development of novel therapeutics for the treatment of hypertension and other vascular diseases. The present review considers recent findings regarding the ACE2/Ang-(1–7) signaling and focuses on its regulatory roles in processes related to proliferation, inflammation, vascular fibrosis and remodeling, providing proof of principle for the potential use of ACE2 as a novel therapy for vascular disorders related to vascular remodeling.
机译:肾素-血管紧张素系统(RAS)调节血管紧张度并在血管重构中起关键作用,这是血管紧张度和结构变化复杂相互作用的结果。抑制RAS已导致预防和治疗血管疾病如高血压,糖尿病性血管病和动脉粥样硬化的重要药理学工具。血管紧张素转换酶2(ACE2)最近被鉴定为负责将血管紧张素(Ang)II转化为Ang-(1-7)的多功能单羧肽酶。 ACE2 / Ang-(1-7)信号可防止细胞增殖,病理性肥大,氧化应激和血管纤维化。因此,ACE2 / Ang-(1-7)信号作为RAS的负调节剂被认为对心血管系统有益。将ACE2 / Ang-(1-7)信号添加到RAS的复杂性可能会导致开发用于治疗高血压和其他血管疾病的新型疗法。本综述考虑了有关ACE2 / Ang-(1-7)信号传导的最新发现,并着重于其在与增殖,炎症,血管纤维化和重塑有关的过程中的调节作用,为ACE2作为一种新型药物的潜在用途提供了原理证明。与血管重塑有关的血管疾病的疗法。

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