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阿普西坦,一种正在研发用于治疗顽固性高血压的双重内皮素受体拮抗剂。

Aprocitentan, A Dual Endothelin Receptor Antagonist Under Development for the Treatment of Resistant Hypertension.

作者信息

Angeli Fabio, Verdecchia Paolo, Reboldi Gianpaolo

机构信息

Department of Medicine and Surgery, University of Insubria, Varese, Italy.

Department of Medicine and Cardiopulmonary Rehabilitation, Maugeri Care and Research Institutes, IRCCS Tradate, Varese, Italy.

出版信息

Cardiol Ther. 2021 Dec;10(2):397-406. doi: 10.1007/s40119-021-00233-7. Epub 2021 Jul 12.

Abstract

Aprocitentan (ACT-132577) is an orally active, dual endothelin-1 (ET-1) receptor antagonist that prevents the binding of ET-1 to both ETA/ETB receptors. It is an active metabolite of macitentan (obtained by oxidative depropylation), an orphan drug used for the treatment of pulmonary arterial hypertension. Aprocitentan is highly bound to plasma proteins and is eliminated in both urine and feces. It is well tolerated across all doses (up to 600 mg with single dose and 100 mg once a day at multiple doses). Its pharmacokinetic profile shows a half-life of 44 h, fitting a once-daily dosing regimen with plasma ET-1 concentrations (reflecting ET receptor antagonism), significantly increasing with doses ≥ 25 mg. Only minor differences in exposure between healthy females and males, healthy elderly and adult subjects, fed and fasted conditions, and renal function have been observed. Aprocitentan in patients with resistant hypertension is currently under investigation in the PRECISION phase III trial (ClinicalTrials identifier: NCT03541174). Nonetheless, results of pre-clinical data and studies in humans support the potential role of aprocitentan in this clinical setting. The absolute blood pressure (BP) reductions with aprocitentan are in the ranges established as a surrogate for reduction in cardiovascular morbidity in hypertension. Significant changes in BP with aprocitentan are observed within 14 days, and its BP-lowering effects have also been documented with ambulatory BP monitoring. Finally, aprocitentan enhances the BP-lowering effects of other antihypertensive drugs, including renin-angiotensin-system blockers. In conclusion, aprocitentan ameliorates the effects of ET-1 and could potentially reduce BP and provide broader cardiovascular protection in patients with resistant hypertension. Available data support the hypothesis that this new agent could expand our antihypertensive arsenal in resistant hypertension, making aprocitentan an attractive candidate for further large-scale trials.

摘要

阿朴西坦(ACT-132577)是一种口服活性的双重内皮素-1(ET-1)受体拮抗剂,可阻止ET-1与ETA/ETB受体结合。它是马西替坦的活性代谢产物(通过氧化去丙基化获得),马西替坦是一种用于治疗肺动脉高压的孤儿药。阿朴西坦与血浆蛋白高度结合,经尿液和粪便排泄。在所有剂量下(单剂量高达600mg,多剂量为每日一次100mg)耐受性良好。其药代动力学特征显示半衰期为44小时,适合每日一次给药方案,血浆ET-1浓度(反映ET受体拮抗作用)随剂量≥25mg显著增加。在健康女性和男性、健康老年人和成年人、进食和空腹状态以及肾功能之间,仅观察到暴露方面的微小差异。阿朴西坦用于治疗顽固性高血压的患者目前正在进行PRECISION III期试验(临床试验标识符:NCT03541174)。尽管如此,临床前数据和人体研究结果支持阿朴西坦在这种临床情况下的潜在作用。阿朴西坦导致的绝对血压(BP)降低幅度处于已确定的作为高血压心血管发病率降低替代指标的范围内。使用阿朴西坦后14天内可观察到BP的显著变化,动态血压监测也记录了其降压效果。最后,阿朴西坦可增强其他降压药物的降压效果,包括肾素-血管紧张素系统阻滞剂。总之,阿朴西坦可改善ET-1的作用,并可能降低BP,为顽固性高血压患者提供更广泛的心血管保护。现有数据支持这一假说,即这种新药可扩充我们用于治疗顽固性高血压的抗高血压药物库,使阿朴西坦成为进一步大规模试验的有吸引力的候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db5/8555037/f28f0d5455be/40119_2021_233_Fig1_HTML.jpg

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