NILVADIPINE - PROFILE OF A NEW CALCIUM-ANTAGONIST - AN OVERVIEW

被引:17
|
作者
ROSENTHAL, J
机构
关键词
NILVADIPINE; PHARMACOKINETIC PROPERTIES; PHARMACODYNAMIC PROPERTIES; HYPERTENSION;
D O I
10.1097/00005344-199406242-00014
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 (RR(diast) <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.
引用
收藏
页码:S92 / S107
页数:16
相关论文
共 50 条
  • [21] EFONIDIPINE HYDROCHLORIDE - A NEW CALCIUM-ANTAGONIST
    MASUDA, Y
    TANAKA, S
    CARDIOVASCULAR DRUG REVIEWS, 1994, 12 (02): : 123 - 135
  • [22] WHY A NEW CALCIUM-ANTAGONIST - INTRODUCTION
    ZANCHETTI, A
    JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1991, 17 : R5 - R7
  • [23] EFFICACY AND DISPOSITION OF A NEW CALCIUM-ANTAGONIST
    SCHNECK, DW
    RUBIN, A
    KNADLER, MP
    BOWSHER, R
    APATHY, J
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 1987, 41 (02) : 234 - 234
  • [24] NEW VASODILATOR CALCIUM-ANTAGONIST FORIDON
    VITOLINYA, RO
    KIMENIS, AA
    KHIMIKO-FARMATSEVTICHESKII ZHURNAL, 1989, 23 (07): : 889 - 892
  • [25] EFFECT OF A NEW CALCIUM-ANTAGONIST, NILVADIPINE, ON VARIANT ANGINA-PECTORIS EVALUATED BY 24-HOUR HOLTER ELECTROCARDIOGRAPHY
    KISHIDA, H
    TOYAMA, S
    YANAGA, T
    SUZUKI, K
    JAPANESE HEART JOURNAL, 1988, 29 (06): : 781 - 793
  • [26] ANTIHYPERTENSIVE EFFECT OF THE CALCIUM-ANTAGONIST ISRADIPINE AND LIPID PROFILE
    FARSANG, C
    KISS, I
    KAPOCSI, J
    TOROK, E
    MAKLARI, E
    AMERICAN JOURNAL OF HYPERTENSION, 1993, 6 (03) : S107 - S109
  • [27] EFFECT OF THE CALCIUM-ANTAGONIST NILVADIPINE ON HEMODYNAMICS AT REST AND DURING COLD STIMULATION IN ESSENTIAL-HYPERTENSION
    TAKABATAKE, T
    YAMAMOTO, Y
    NAKAMURA, S
    HASHIMOTO, N
    SATOH, S
    YAMADA, Y
    OHTA, H
    HATTORI, N
    EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1987, 33 (03) : 215 - 219
  • [28] CARDIOVASCULAR EFFECTS OF NISOLDIPINE, A NEW CALCIUM-ANTAGONIST
    FEIGEN, LP
    KING, LW
    BECKETT, W
    KADOWITZ, PJ
    FEDERATION PROCEEDINGS, 1982, 41 (05) : 1648 - 1648
  • [29] ANTIATHEROSCLEROTIC EFFECTS OF NEW CALCIUM-ANTAGONIST, ANIPAMIL
    OREKHOV, AN
    TERTOV, VV
    ARTERIOSCLEROSIS, 1989, 9 (05): : A756 - A756
  • [30] EFFECTIVENESS OF A NEW CALCIUM-ANTAGONIST IN SEVERE HYPERTENSION
    BURRIS, JF
    SANTANGELO, RP
    MROCZEK, WJ
    JOURNAL OF CLINICAL PHARMACOLOGY, 1986, 26 (08): : 593 - 597