首页> 美国卫生研究院文献>Pharmacological Reviews >Novel Therapeutic Approaches Targeting the Renin-Angiotensin System and Associated Peptides in Hypertension and Heart Failure
【2h】

Novel Therapeutic Approaches Targeting the Renin-Angiotensin System and Associated Peptides in Hypertension and Heart Failure

机译:针对高血压和心力衰竭的肾素-血管紧张素系统和相关肽的新型治疗方法

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Despite the success of renin-angiotensin system (RAS) blockade by angiotensin-converting enzyme (ACE) inhibitors and angiotensin II type 1 receptor (AT1R) blockers, current therapies for hypertension and related cardiovascular diseases are still inadequate. Identification of additional components of the RAS and associated vasoactive pathways, as well as new structural and functional insights into established targets, have led to novel therapeutic approaches with the potential to provide improved cardiovascular protection and better blood pressure control and/or reduced adverse side effects. The simultaneous modulation of several neurohumoral mediators in key interconnected blood pressure–regulating pathways has been an attractive approach to improve treatment efficacy, and several novel approaches involve combination therapy or dual-acting agents. In addition, increased understanding of the complexity of the RAS has led to novel approaches aimed at upregulating the ACE2/angiotensin-(1-7)/Mas axis to counter-regulate the harmful effects of the ACE/angiotensin II/angiotensin III/AT1R axis. These advances have opened new avenues for the development of novel drugs targeting the RAS to better treat hypertension and heart failure. Here we focus on new therapies in preclinical and early clinical stages of development, including novel small molecule inhibitors and receptor agonists/antagonists, less conventional strategies such as gene therapy to suppress angiotensinogen at the RNA level, recombinant ACE2 protein, and novel bispecific designer peptides.
机译:尽管通过血管紧张素转换酶(ACE)抑制剂和血管紧张素II 1型受体(AT1R)阻断剂成功地阻断了肾素-血管紧张素系统(RAS),但目前对高血压和相关心血管疾病的治疗仍然不足。 RAS附加成分的识别和相关的血管活性途径,以及对既定目标的新结构和功能见解,已导致了新颖的治疗方法,有望提供改善的心血管保护和更好的血压控制和/或减少不良副作用。在关键的相互联系的血压调节途径中同时调节几种神经体液介质是提高治疗效果的一种有吸引力的方法,并且几种新方法涉及联合治疗或双重作用药物。此外,对RAS复杂性的更多了解导致了旨在上调ACE2 /血管紧张素-(1-7)/ Mas轴以反调节ACE /血管紧张素II /血管紧张素III / AT1R的有害作用的新颖方法轴。这些进展为针对RAS的新药开发开辟了新途径,以更好地治疗高血压和心力衰竭。在这里,我们将重点放在临床前和临床早期发展阶段的新疗法,包括新型小分子抑制剂和受体激动剂/拮抗剂,较不常规的策略,例如在RNA水平上抑制血管紧张素原的基因治疗,重组ACE2蛋白和新型双特异性设计肽。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号