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靶向心肌肥厚:迈向因果性心力衰竭治疗

Targeting cardiac hypertrophy: toward a causal heart failure therapy.

作者信息

Bisping Egbert, Wakula Paulina, Poteser Michael, Heinzel Frank R

机构信息

*Division of Cardiology, Medical University of Graz, Graz, Austria; †Ludwig Boltzmann Institute for Translational Heart Failure Research, Graz, Austria; and ‡Institute for Biophysics, Graz, Austria.

出版信息

J Cardiovasc Pharmacol. 2014 Oct;64(4):293-305. doi: 10.1097/FJC.0000000000000126.

Abstract

Cardiac hypertrophy is commonly observed in conditions of increased hemodynamic or metabolic stress. This hypertrophy is not compensatory but rather reflects activation of maladaptive cellular processes that promote disease progression. Myocardial hypertrophy serves as a diagnostic and prognostic marker of cardiac remodeling, and underlying regulatory processes have provided effective therapeutic targets to slow disease progression and improve outcome. We review hypertrophic signaling pathways in cardiomyocytes and discuss established and novel targets for pharmacological intervention. New drugs in the pipeline include the third generation aldosterone antagonists (PF-03882845 and BAY94-8862) and biased angiotensin II receptor agonists. Furthermore, different approaches to stimulate cGMP-dependent protective signaling are currently evaluated in clinical trials, including the combination of the vasopeptidase neprilysin inhibitor and an angiotensin receptor blocker (ARNi). In an overview on cardiomyocyte hypertrophic signaling, we also highlight emerging experimental treatment concepts such as inhibition of Ca-mediated transcriptional regulation, adeno-associated viruses for sarcoplasmic/endoplasmic reticulum calcium ATPase (SERCA2a), PI3 kinase gene transfer and microRNA-based therapy. We conclude that antihypertrophic therapy extends beyond blocking the classical β-adrenergic and renin-angiotensin-aldosterone system-dependent signaling cascades, although new therapies require clinical validation regarding outcome.

摘要

心脏肥大常见于血流动力学或代谢应激增加的情况下。这种肥大并非代偿性的,而是反映了促进疾病进展的适应性不良细胞过程的激活。心肌肥大是心脏重塑的诊断和预后标志物,其潜在的调节过程为减缓疾病进展和改善预后提供了有效的治疗靶点。我们综述了心肌细胞中的肥大信号通路,并讨论了已确立的和新的药物干预靶点。正在研发的新药包括第三代醛固酮拮抗剂(PF-03882845和BAY94-8862)和偏向性血管紧张素II受体激动剂。此外,目前正在临床试验中评估刺激环鸟苷酸依赖性保护信号的不同方法,包括血管肽酶中性肽链内切酶抑制剂和血管紧张素受体阻滞剂(ARNi)的联合使用。在对心肌细胞肥大信号的综述中,我们还强调了新兴的实验性治疗概念,如抑制钙介导的转录调控、用于肌浆网/内质网钙ATP酶(SERCA2a)的腺相关病毒、PI3激酶基因转移和基于微小RNA的治疗。我们得出结论,抗肥大治疗不仅仅局限于阻断经典的β-肾上腺素能和肾素-血管紧张素-醛固酮系统依赖性信号级联反应,尽管新疗法需要在疗效方面进行临床验证。

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