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[钙通道阻滞剂在高血压和缺血性冠心病治疗中的应用。评估中的争议]

[Calcium channel blockers in the treatment of hypertension and ischemic coronary disease. Conflicts in their evaluation].

作者信息

Mayer O

机构信息

Oddĕlení klinické farmakologie, FN, Plzen.

出版信息

Cas Lek Cesk. 1998 Apr 6;137(7):216-9.

PMID:9650344
Abstract

Calcium channel blockers represent a pharmacologically non homogenic group. Verapamil and diltiazem have myocardial component of their effect, which acts against activated sympathicus. Short acting dihydropyridines (nifedipin) appear to be harmful by patients after myocardial infarction which is caused by the reflex sympathetic response to the predominant vasodilation. In the treatment of cardiovascular disease (e.g. hypertension, coronary vascular disease) are short acting dihydropyridines not recommended. Dihydropyridines of the new generation (amlodipin, felodipin, isradipin, lacidipin, nicardipin, nimodipin, nisoldipin, nitrendipin) induce less tachycardia due to their favorable kinetic features. If the slow movement in blood or at the receptor site is not a result of molecule features there is necessary to use retarded preparations of active substance. Nevertheless, commonly used retarded preparations fulfil this requirement only incompletely. The desirable quality is provided by modern form of retardation. (e.g. GITS) only.

摘要

钙通道阻滞剂是一类药理学上非同源的药物。维拉帕米和地尔硫䓬具有心肌作用成分,可对抗激活的交感神经。短效二氢吡啶类(硝苯地平)对心肌梗死后的患者似乎有害,这是由对主要血管扩张的反射性交感反应引起的。在治疗心血管疾病(如高血压、冠状动脉疾病)时,不推荐使用短效二氢吡啶类药物。新一代二氢吡啶类(氨氯地平、非洛地平、伊拉地平、拉西地平、尼卡地平、尼莫地平、尼索地平、尼群地平)由于其良好的动力学特性,引起的心动过速较少。如果血液中或受体部位的缓慢移动不是分子特性的结果,则需要使用活性物质的缓释制剂。然而,常用的缓释制剂仅不完全满足这一要求。理想的质量仅由现代缓释形式(如控释片)提供。

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