Cataliotti Alessandro, Burnett John C
Mayo Clinic College of Medicine, Division of Cardiovascular Diseases, Department of Internal Medicine, Rochester, MN 55905, USA.
J Investig Med. 2005 Nov;53(7):378-84. doi: 10.2310/6650.2005.53711.
Since the discovery of the cardiac hormone atrial natriuretic peptide by de Bold and colleagues in 1981, the field of natriuretic peptides has significantly advanced with translation of new knowledge to the clinical practice of heart failure. This new knowledge builds on the importance of cardiorenal mechanisms that contribute to optimal cardiovascular regulation. Recent investigations by our group and others have also established the direct myocardial actions of the natriuretic peptides, broadening their therapeutic potential beyond renal mechanisms. Indeed, a potential therapeutic target is cardiac remodeling and fibrosis based on the unique cardiorenal and humoral protective properties that natriuretic peptides possess. We review new insights into the natriuretic peptide system and specifically focus on the possible role of natriuretic peptides as a new therapeutic strategy to limit cardiac remodeling and fibrosis to delay worsening of cardiac function and the progression of heart failure.
自1981年德博尔德及其同事发现心脏激素心房利钠肽以来,利钠肽领域随着新知识转化为心力衰竭的临床实践而取得了显著进展。这一新知识建立在对有助于优化心血管调节的心脏-肾脏机制的重要性的认识之上。我们团队和其他团队最近的研究还证实了利钠肽对心肌的直接作用,拓宽了其在肾脏机制之外的治疗潜力。事实上,基于利钠肽所具有的独特的心脏-肾脏和体液保护特性,一个潜在的治疗靶点是心脏重塑和纤维化。我们回顾了对利钠肽系统的新见解,并特别关注利钠肽作为一种新的治疗策略的可能作用,以限制心脏重塑和纤维化,延缓心功能恶化和心力衰竭的进展。