Literature DB >> 2196168

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

H A Friedel1, R N Brogden.   

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.

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Year:  1990        PMID: 2196168     DOI: 10.2165/00003495-199039060-00008

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  95 in total

1.  Comparison of antihypertensive, renal hemodynamic, and humoral effects of pinacidil and hydralazine monotherapy.

Authors:  P A Abraham; C E Halstenson; G R Matzke; W F Keane
Journal:  J Clin Hypertens       Date:  1987-12       Impact factor: 3.738

2.  Pinacidil inhibits insulin release by increasing K+ outflow from pancreatic B-cells.

Authors:  P Lebrun; V Devreux; M Hermann; A Herchuelz
Journal:  Eur J Pharmacol       Date:  1988-11-01       Impact factor: 4.432

3.  Pinacidil: history, basic pharmacology, and therapeutic implications.

Authors:  I Ahnfelt-Rønne
Journal:  J Cardiovasc Pharmacol       Date:  1988       Impact factor: 3.105

4.  Systemic and coronary hemodynamic effects of pinacidil, a new antihypertensive agent, in awake dogs: comparison with hydralazine.

Authors:  S Kawashima; C S Liang
Journal:  J Pharmacol Exp Ther       Date:  1985-02       Impact factor: 4.030

5.  Evidence that the mechanism of the inhibitory action of pinacidil in rat and guinea-pig smooth muscle differs from that of glyceryl trinitrate.

Authors:  K M Bray; D T Newgreen; R C Small; J S Southerton; S G Taylor; S W Weir; A H Weston
Journal:  Br J Pharmacol       Date:  1987-06       Impact factor: 8.739

6.  Age-dependence of the effects of pinacidil on rat aorta.

Authors:  J C Wanstall; S R O'Donnell; X P Zeng
Journal:  J Pharm Pharmacol       Date:  1989-09       Impact factor: 3.765

7.  Pinacidil, a new vasodilator, in the treatment of mild to moderate essential hypertension.

Authors:  V D'Arcy; M Laher; D McCoy; P Sullivan; C H Walsh; M P Hickey
Journal:  Eur J Clin Pharmacol       Date:  1985       Impact factor: 2.953

8.  Vasodilator monotherapy in the treatment of hypertension: comparative efficacy and safety of pinacidil, a potassium channel opener, and prazosin.

Authors:  M R Goldberg; C S Sushak; F W Rockhold; W L Thompson
Journal:  Clin Pharmacol Ther       Date:  1988-07       Impact factor: 6.875

9.  In vitro studies on the mode of action of pinacidil.

Authors:  A H Weston; K M Bray; S Duty; A D McHarg; D T Newgreen; J S Southerton
Journal:  Drugs       Date:  1988       Impact factor: 9.546

10.  Inhibition of platelet aggregation and thromboxane production by pinacidil.

Authors:  R P Goodman; D M Little; J T Wright
Journal:  Prostaglandins Leukot Med       Date:  1985-08
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  13 in total

Review 1.  Nitrile-containing pharmaceuticals: efficacious roles of the nitrile pharmacophore.

Authors:  Fraser F Fleming; Lihua Yao; P C Ravikumar; Lee Funk; Brian C Shook
Journal:  J Med Chem       Date:  2010-08-30       Impact factor: 7.446

Review 2.  Potassium channel openers. Pharmacological effects and future uses.

Authors:  S Duty; A H Weston
Journal:  Drugs       Date:  1990-12       Impact factor: 9.546

Review 3.  K(ATP) channel therapeutics at the bedside.

Authors:  A Jahangir; Andre Terzic
Journal:  J Mol Cell Cardiol       Date:  2005-07       Impact factor: 5.000

Review 4.  Electrophysiologic effects of potassium channel openers.

Authors:  W Haverkamp; M Borggrefe; G Breithardt
Journal:  Cardiovasc Drugs Ther       Date:  1995-03       Impact factor: 3.727

Review 5.  Pharmacology of the potassium channel openers.

Authors:  G Edwards; A H Weston
Journal:  Cardiovasc Drugs Ther       Date:  1995-03       Impact factor: 3.727

Review 6.  K+ channel opening: a new drug principle in cardiovascular medicine.

Authors:  J E Nielsen-Kudsk; S Boesgaard; J Aldershvile
Journal:  Heart       Date:  1996-08       Impact factor: 5.994

7.  Modifications by chronic intermittent hypoxia and drug treatment on skeletal muscle metabolism.

Authors:  O Pastoris; M Dossena; P Foppa; R Arnaboldi; A Gorini; R F Villa; G Benzi
Journal:  Neurochem Res       Date:  1995-02       Impact factor: 3.996

Review 8.  Nicorandil. A review of its pharmacology and therapeutic efficacy in angina pectoris.

Authors:  J Frampton; M M Buckley; A Fitton
Journal:  Drugs       Date:  1992-10       Impact factor: 9.546

9.  Contribution of Na+ -Ca2+ exchanger to pinacidil-induced relaxation in the rat mesenteric artery.

Authors:  Suk Ying Tsang; Xiaoqiang Yao; Chi Ming Wong; Chak Leung Au; Zhen Yu Chen; Yu Huang
Journal:  Br J Pharmacol       Date:  2003-02       Impact factor: 8.739

10.  Comparison of the effects of several potassium-channel openers on rat bladder and rat portal vein in vitro.

Authors:  G Edwards; M Henshaw; M Miller; A H Weston
Journal:  Br J Pharmacol       Date:  1991-03       Impact factor: 8.739

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