Coca Antonio, Mazón Pilar, Aranda Pedro, Redón Josep, Divisón Juan Antonio, Martínez Javier, Calvo Carlos, Galcerán Josep María, Barrios Vivencio, Roca-Cusachs I Coll Alexandre
Department of Internal Medicine, Hypertension Unit, Institute of Medicine & Dermatology, Hospital Clínico, University of Barcelona, Barcelona, Spain.
Expert Rev Cardiovasc Ther. 2013 Jan;11(1):91-105. doi: 10.1586/erc.12.155.
Dihydropyridinic calcium channel blockers are a subclass of antihypertensive drugs with growing significance in the therapeutic armamentarium. Early studies in the 1990s had aroused certain fears with regard to the safety of the first drugs from this class, since they had a fast onset of action and a short half-life, and thus they were associated with reflex adrenergic activation. New molecules with long half-lives and high lipophilia have shown safety and efficacy in the control of blood pressure, as well as in the reduction of several end points related to hypertension. Moreover, these new molecules, which block special subtypes of calcium channel receptors, provide drugs not only with an action profile that goes beyond the antihypertensive effect, but also with a lower rate of side effects. Therefore, in the light of new studies that include calcium channel blockers alone or in combination, these agents will probably be used even more extensively for the management of hypertension in the following years.
二氢吡啶类钙通道阻滞剂是一类抗高血压药物,在治疗药物库中的重要性日益增加。20世纪90年代的早期研究引发了对该类首批药物安全性的某些担忧,因为它们起效迅速且半衰期短,因此与反射性肾上腺素能激活有关。具有长半衰期和高亲脂性的新分子已在血压控制以及降低与高血压相关的几个终点方面显示出安全性和有效性。此外,这些阻断钙通道受体特殊亚型的新分子不仅为药物提供了超越抗高血压作用的作用谱,而且副作用发生率更低。因此,鉴于包括单独或联合使用钙通道阻滞剂的新研究,这些药物在未来几年可能会更广泛地用于高血压的管理。