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尼伐地平:一种新型钙拮抗剂的概况。综述。

Nilvadipine: profile of a new calcium antagonist. An overview.

作者信息

Rosenthal J

机构信息

Section of Pharmacotherapy, University of Ulm, Germany.

出版信息

J Cardiovasc Pharmacol. 1994;24 Suppl 2:S92-107.

PMID:7898101
Abstract

Nilvadipine is a new calcium antagonist of the the dihydropyridine group. Owing to its high receptor affinity, nilvadipine blocks L-type calcium channels in vascular muscle cells. This leads to prolonged vascular relaxation and lowering of blood pressure. In comparison with nifedipine, the prototype of the dihydropyridines, nilvadipine possesses special pharmacokinetic and pharmacodynamic properties. The duration of action is longer, and the vasodilatory effect is 5-16 times greater. Compared with nifedipine, the cardiodepressive action and the adrenergic counterregulation are less intense for nilvadipine. Nilvadipine's higher vasoselectivity is expressed in a vascular/cardiac efficacy quotient of 251, is 9-10 times higher than that of nifedipine. In therapeutic dosages nilvadipine has no negative inotropic, chronotropic, or dromotropic effects. In various in vitro and animal experiments, nilvadipine demonstrated a good antiatherogenic action. Nilvadipine is absorbed quickly and completely. Owing to a marked first-pass effect, the absolute bioavailability is 14-19%. The final elimination half-life is between 15 and 20 h, probably due to slow redistribution from the tissue. Nilvadipine is mainly excreted via the kidneys in the form of inactive metabolites. The pharmaceutical preparation as a depot form prevents an over-increase of the plasma level, and therefore reduces the typical side effects of dihydropyridine calcium antagonists. The pharmacokinetics of nilvadipine are not affected by reduced renal function. The bioavailability is increased in liver cirrhosis, but with repeated administration no cumulative effect takes place. Because of nilvadipine's long half-life, a once-daily administration is adequate to reduce blood pressure over 24 h in the treatment of arterial hypertension. At a daily dosage of 8-16 mg, the responder rate (RRdiast < 90 mm Hg) is 60-70% in single-drug therapy and up to 80% in combination therapy. Nilvadipine can be used to treat hypertensive patients who are also suffering from diabetes mellitus, lipometabolic disturbances, chronic obstructive respiratory tract disease, or cerebral circulatory disturbances. Owing to its high vascular selectivity, antiatherogenic properties, 24-h action, and good tolerance, nilvadipine fulfills the requirements for a modern antihypertensive agent.

摘要

尼伐地平是一种新型的二氢吡啶类钙拮抗剂。由于其对受体的高亲和力,尼伐地平可阻断血管平滑肌细胞中的L型钙通道。这会导致血管舒张时间延长和血压降低。与二氢吡啶类的原型硝苯地平相比,尼伐地平具有特殊的药代动力学和药效学特性。其作用持续时间更长,血管舒张作用强5至16倍。与硝苯地平相比,尼伐地平的心脏抑制作用和肾上腺素能反向调节作用较弱。尼伐地平较高的血管选择性表现为血管/心脏效能商为251,比硝苯地平高9至10倍。在治疗剂量下,尼伐地平没有负性肌力、负性频率或负性传导作用。在各种体外和动物实验中,尼伐地平显示出良好的抗动脉粥样硬化作用。尼伐地平吸收迅速且完全。由于明显的首过效应,绝对生物利用度为14%至19%。最终消除半衰期在15至20小时之间,这可能是由于从组织中缓慢再分布所致。尼伐地平主要以无活性代谢产物的形式经肾脏排泄。作为长效剂型的药物制剂可防止血浆水平过度升高,因此减少了二氢吡啶类钙拮抗剂的典型副作用。尼伐地平的药代动力学不受肾功能降低的影响。在肝硬化患者中生物利用度会增加,但重复给药不会产生累积效应。由于尼伐地平半衰期长,每日一次给药足以在治疗动脉高血压时24小时内降低血压。在单药治疗中,每日剂量为8至16毫克时,有效率(舒张压<90毫米汞柱)为60%至70%,联合治疗时可达80%。尼伐地平可用于治疗同时患有糖尿病、脂质代谢紊乱、慢性阻塞性呼吸道疾病或脑循环障碍的高血压患者。由于其高血管选择性、抗动脉粥样硬化特性、24小时作用时间和良好的耐受性,尼伐地平符合现代抗高血压药物的要求。

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