Suppr超能文献

当前和未来针对心血管疾病内皮素途径的靶向策略。

Current and future strategies for targeting the endothelin pathway in cardiovascular disease.

机构信息

Division of Experimental Medicine and Immunotherapeutics, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK.

Royal Papworth Hospital NHS Foundation Trust, Cambridge Biomedical Campus, Cambridge, UK.

出版信息

Nat Cardiovasc Res. 2023 Nov;2(11):972-990. doi: 10.1038/s44161-023-00347-2. Epub 2023 Nov 2.

Abstract

The first endothelin (ET)-1 receptor antagonist was approved for clinical use over 20 years ago, but to date this class of compounds has been limited to treating pulmonary arterial hypertension, a rare disease. Translational research over the last 5 years has reignited interest in the ET system as a therapeutic target across the spectrum of cardiovascular diseases including resistant hypertension, microvascular angina and post-coronavirus disease 2019 conditions. Notable developments include approval of a new ET receptor antagonist and, intriguingly, combining the actions of ET and an angiotensin II type 1 receptor antagonist within the same novel small molecule. Combinations of ET receptor blockers with other drugs, including phosphodiesterase-5 inhibitors and sodium-glucose co-transporter-2 antagonists, may drive synergistic benefits with the prospect of alleviating side effects. These new therapeutic strategies have the potential to dramatically widen the scope of indications targeting the ET-1 pathway.

摘要

20 多年前,首个内皮素(ET)-1 受体拮抗剂获批临床应用,但迄今为止,此类化合物仅限于治疗肺动脉高压这一罕见疾病。过去 5 年的转化研究再次激发了人们对 ET 系统作为治疗靶点的兴趣,涵盖了心血管疾病的各个方面,包括耐药性高血压、微血管性心绞痛和新冠病毒病 2019 后的状况。值得注意的进展包括一种新型 ET 受体拮抗剂的获批,以及在同一新型小分子中结合 ET 和血管紧张素 II 型 1 受体拮抗剂的作用。ET 受体阻滞剂与其他药物(包括磷酸二酯酶-5 抑制剂和钠-葡萄糖共转运蛋白-2 拮抗剂)的联合应用可能会带来协同效益,并有望减轻副作用。这些新的治疗策略有可能极大地拓宽靶向 ET-1 途径的适应证范围。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验