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心脏血管系统中阿片促黑素皮质素原系统与 ACE2 的相互作用:治疗意义。

Interaction between the apelinergic system and ACE2 in the cardiovascular system: therapeutic implications.

机构信息

Department of Physiology, University of Alberta, Edmonton, Alberta, Canada.

Mazankowski Alberta Heart Institute, Edmonton, Alberta, Canada.

出版信息

Clin Sci (Lond). 2020 Sep 18;134(17):2319-2336. doi: 10.1042/CS20200479.

Abstract

The apelinergic system is widely expressed and acts through autocrine and paracrine signaling to exert protective effects, including vasodilatory, metabolic, and inotropic effects on the cardiovascular (CV) system. The apelin pathway's dominant physiological role has delineated therapeutic implications for coronary artery disease, heart failure (HF), aortic aneurysm, pulmonary arterial hypertension (PAH), and transplant vasculopathy. Apelin peptides interact with the renin-angiotensin system (RAS) by promoting angiotensin converting enzyme 2 (ACE2) transcription leading to increased ACE2 protein and activity while also antagonizing the effects of angiotensin II (Ang II). Apelin modulation of the RAS by increasing ACE2 action is limited due to its rapid degradation by proteases, including ACE2, neprilysin (NEP), and kallikrein. Apelin peptides are hence tightly regulated in a negative feedback manner by ACE2. Plasma apelin levels are suppressed in pathological conditions, but its diagnostic and prognostic utility requires further clinical exploration. Enhancing the beneficial actions of apelin peptides and ACE2 axes while complementing existing pharmacological blockade of detrimental pathways is an exciting pathway for developing new therapies. In this review, we highlight the interaction between the apelin and ACE2 systems, discuss their pathophysiological roles and potential for treating a wide array of CV diseases (CVDs).

摘要

阿片素能系统广泛表达,并通过自分泌和旁分泌信号发挥保护作用,包括对心血管系统的血管舒张、代谢和变力作用。阿片素途径的主要生理作用为冠状动脉疾病、心力衰竭 (HF)、主动脉瘤、肺动脉高压 (PAH) 和移植血管病的治疗提供了启示。阿片素肽通过促进血管紧张素转换酶 2 (ACE2) 的转录与肾素-血管紧张素系统 (RAS) 相互作用,导致 ACE2 蛋白和活性增加,同时拮抗血管紧张素 II (Ang II) 的作用。阿片素通过增加 ACE2 作用对 RAS 的调节受到限制,因为其被包括 ACE2、脑啡肽酶 (NEP) 和激肽释放酶在内的蛋白酶迅速降解。因此,阿片素肽通过 ACE2 以负反馈的方式被严格调节。在病理条件下,血浆阿片素水平受到抑制,但它的诊断和预后效用需要进一步的临床探索。增强阿片素肽和 ACE2 轴的有益作用,同时补充现有有害途径的药理学阻断,是开发新疗法的令人兴奋的途径。在这篇综述中,我们强调了阿片素和 ACE2 系统之间的相互作用,讨论了它们的病理生理作用及其在治疗广泛心血管疾病 (CVDs) 方面的潜力。

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