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Pinacidil. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in the treatment of hypertension.

作者信息

Friedel H A, Brogden R N

机构信息

ADIS Drug Information Services, Auckland, New Zealand.

出版信息

Drugs. 1990 Jun;39(6):929-67. doi: 10.2165/00003495-199039060-00008.

DOI:10.2165/00003495-199039060-00008
PMID:2196168
Abstract

Pinacidil is an orally administered antihypertensive drug that acts via direct relaxation of vascular smooth muscle to produce peripheral vasodilatation and a reduction in blood pressure without significant direct effects on cardiac electrophysiology. Pinacidil is unrelated to other antihypertensive drugs in clinical use, either in structure or mechanism of action. It belongs to a new class of agents called 'potassium channel openers' which act via potassium efflux to hyperpolarize cell membranes, indirectly causing a net reduction in intracellular calcium that leads to relaxation of vascular smooth muscle. Pinacidil is indicated in the management of essential hypertension. In clinical trials of up to 1 year duration, pinacidil administered twice daily in a controlled release capsule formulation has been shown to achieve adequate blood pressure control both in previously untreated patients and in those with blood pressure inadequately controlled by beta-adrenoceptor blocking drugs or thiazide diuretics. In long term (up to 1 year) comparative studies pinacidil was at least as effective as hydralazine, prazosin or nifedipine in maintaining blood pressure control. Pinacidil may also have a potential use in the treatment of patients with secondary renal hypertension. Clinical trials to date have usually allowed the addition of a thiazide diuretic and/or beta-adrenoceptor blocking drug to enhance the efficacy of pinacidil and/or to reduce the incidence of adverse effects. The main adverse effects of pinacidil treatment, which result from its peripheral vasodilator activity, are headache, oedema, palpitations and tachycardia. Although the overall incidence of adverse effects is quite high, they are usually mild, transient in nature and respond to a reduction in dose. Nevertheless, these effects may occasionally be severe, necessitating withdrawal from therapy. Thus, pinacidil is an effective antihypertensive drug for the treatment of mild to moderate essential hypertension. Despite its novel mechanism of action pinacidil causes adverse effects typical of peripheral vasodilators; during long term use with twice daily administration of the controlled release capsule formulation, the addition of a diuretic is often necessary to attenuate peripheral oedema and maintain adequate control of blood pressure. Further long term controlled trials are needed to determine the precise role of pinacidil relative to that of the angiotensin converting enzyme (ACE) inhibitors and calcium channel blocking drugs.

摘要

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Experientia. 1980 Apr 15;36(4):445-7. doi: 10.1007/BF01975139.
2
Effect of a new vasodilator, pinacidil (P 1134), on potassium, noradrenaline and serotonin induced contractions in rabbit vascular tissues.新型血管扩张剂匹那地尔(P 1134)对兔血管组织中钾、去甲肾上腺素和5-羟色胺诱导收缩的影响。
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Comparison of the effects of a new vasodilator pinacidil and nifedipine on isolated blood vessels.
鉴定四种结构不同的 SUR2 内含型 K 通道抑制剂。
Channels (Austin). 2024 Dec;18(1):2398565. doi: 10.1080/19336950.2024.2398565. Epub 2024 Sep 20.
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Pinacidil ameliorates cardiac microvascular ischemia-reperfusion injury by inhibiting chaperone-mediated autophagy of calreticulin.吡那地尔通过抑制钙网织蛋白伴侣介导的自噬来改善心脏微血管缺血再灌注损伤。
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J Neurogastroenterol Motil. 2015 Oct 1;21(4):494-502. doi: 10.5056/jnm15061.
新型血管扩张剂匹那地尔与硝苯地平对离体血管作用的比较。
Acta Pharmacol Toxicol (Copenh). 1982 Nov;51(5):407-12. doi: 10.1111/j.1600-0773.1982.tb01045.x.
4
Metabolism of the new antihypertensive agent pinacidil in rat, dog and man.
Xenobiotica. 1982 Mar;12(3):187-96. doi: 10.3109/00498258209046793.
5
Pharmacokinetics and distribution of the new antihypertensive agent pinacidil in rat, dog and man.新型抗高血压药物匹那地尔在大鼠、犬和人体中的药代动力学及分布
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