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New Developments in the Pharmacological Treatment of Hypertension: Dead-End or a Glimmer at the Horizon?

机译:高血压药理学的新发展:死胡同还是地平线上的微光?

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摘要

Arterial hypertension is the most prevalent controllable disease world-wide. Yet, we still need to further improve blood pressure control, deal with resistant hypertension, and we hope to reduce risk "beyond blood pressure." The number of candidate molecules aspiring for these aims is constantly declining. The new possible approaches to combat high blood pressure include neprilysineutral endopeptidase (NEP) inhibition, particularly when combined with an angiotensin receptor blockade (such as the ARNI, LCZ696), phosphodiesterase 5 (PDE5) inhibition (KD027/Slx-2101), natriuretic agents (PL3994), or a long-lasting vasointestinal peptide (VIP) analogue (PB1046). Other options exploit the protective arm of the renin-angiotensin-aldosterone system by stimulating the angiotensin AT2 receptor (compound 21), the Mas receptor (AVE-0991), or the angiotensin converting enzyme 2. Finally, we review the possibilities how to optimize the use of the available treatment options by using drug combinations or by tailoring therapy to each patient's angiotensin peptide profile.
机译:动脉高血压是全世界最流行的可控制疾病。但是,我们仍然需要进一步改善血压控制,应对顽固性高血压,并希望降低“超出血压”的风险。渴望实现这些目标的候选分子的数量一直在减少。抗高血压的新方法包括抑制脑啡肽酶/中性内肽酶(NEP),特别是与血管紧张素受体阻滞剂(如ARNI,LCZ696),磷酸二酯酶5(PDE5)抑制(KD027 / Slx-2101)结合使用时,利钠药物(PL3994)或长效血管肠肽(VIP)类似物(PB1046)。其他选择通过刺激血管紧张素AT2受体(化合物21),Mas受体(AVE-0991)或血管紧张素转化酶2来利用肾素-血管紧张素-醛固酮系统的保护臂。最后,我们回顾了如何优化的可能性通过使用药物组合或通过针对每个患者的血管紧张素肽谱进行量身定制的疗法来使用可用的治疗方案。

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