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