Hoque Mohammad Z, Arumugham Pradeep, Huda Nazmul, Verma Nitin, Afiniwala Mitul, Karia Darshak H
Albert Einstein Medical Center, Cardiology, 5501 Old York Road, Philadelphia, PA 19141, USA.
Expert Opin Pharmacother. 2009 Sep;10(13):2161-9. doi: 10.1517/14656560903173237.
Conivaptan, the first vasopressin receptor antagonist approved by the FDA, is available for the treatment of hyponatremia in euvolemic and hypervolemic patients. The renin-angiotensin-aldosterone system is activated in heart failure (HF) causing clinical worsening. Arginine vasopressin levels are also elevated in HF. Conivaptan is an effective and FDA approved for the treatment of euvolemic and hypervolemic hyponatremia and may offer an extra treatment option in HF by targeting V(1a) and V(2) receptors. In this article we review the physiology, preclinical studies as well as the human clinical studies on the use of conivaptan and its potential and promise in the treatment of HF.
考尼伐坦是美国食品药品监督管理局(FDA)批准的首个血管加压素受体拮抗剂,可用于治疗血容量正常和血容量过多患者的低钠血症。肾素-血管紧张素-醛固酮系统在心力衰竭(HF)中被激活,导致临床症状恶化。心力衰竭患者的精氨酸血管加压素水平也会升高。考尼伐坦是一种有效的药物,已获FDA批准用于治疗血容量正常和血容量过多的低钠血症,通过作用于V(1a)和V(2)受体,可能为心力衰竭提供一种额外的治疗选择。在本文中,我们综述了考尼伐坦的生理学、临床前研究以及人体临床研究,及其在治疗心力衰竭方面的潜力和前景。