心血管疾病新的激素阻断策略。

C I Johnston, M Naitoh, J Risvanis, N Farina, L M Burrell
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引用次数: 15

摘要

循环是由重叠的血流动力学、结构和神经体液机制控制的。许多激素血管活性物质,主要来源于内皮细胞,也是生长调节剂。虽然神经激素系统参与正常的生理代偿反应,但在充血性心力衰竭等情况下,它们往往变得不适应。通过血管紧张素转换酶(ACE)抑制剂阻断肾素血管紧张素系统的成功已经导致了阻断其他激素系统的努力。中性内肽酶(NEP)是降解利钠肽的主要酶途径,其催化位点与ACE相似。这就产生了同时抑制这两种酶的化合物。这种双ACE/NEP抑制剂在实验性高血压和心力衰竭中显示出前景。类似的双重NEP/ECE(内皮素转换酶)抑制剂正在变得可用。抗利尿激素通过特定的膜受体对血管系统和肾脏有双重作用。特异性口服抗利尿激素受体拮抗剂已经开发出来,它们在高血压、心力衰竭和水肿状态的治疗潜力正在探索中。
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New hormonal blockade strategies in cardiovascular disease.
The circulation is controlled by overlapping haemodynamic, structural and neurohumoral mechanisms. Many hormonal vasoactive substances, mostly derived from endothelial cells, are also growth regulators. Although neurohormonal systems are involved in normal physiological compensatory responses they often become maladaptive in conditions such as congestive heart failure. The success of blocking the renin angiotensin system by angiotensin converting enzyme (ACE) inhibitors has led to efforts to block other hormonal systems. Neutral endopeptidase (NEP), the major enzymatic pathway for degradation of natriuretic peptides, has a similar catalytic site to ACE. This has led to compounds that simultaneously inhibit both enzymes. Such dual ACE/NEP inhibitors show promise in experimental hypertension and heart failure. Similar dual NEP/ECE (endothelin converting enzyme) inhibitors are becoming available. The hormone vasopressin has dual actions on the vasculature and the kidney via specific membrane receptors. Specific orally active vasopressin receptor antagonists have been developed and their therapeutic potential in hypertension, heart failure and oedematous states are being explored.
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