Literature DB >> 2466175

Pinacidil actions on ion channels in vascular muscle.

R K Hermsmeyer1.   

Abstract

Electrophysiological and mechanical recordings from isolated single vascular muscle cells and isolated segments of caudal artery showed that pinacidil caused vascular muscle relaxation and hyperpolarization which originates from increased K+ conductance. Voltage-clamp recordings of current flow through single K+ channels strongly suggest that pinacidil increases the specific type of K+ conductance associated with the Ca2+-dependent "big" K+ channel (unit conductance of 200 pS in symmetrical K+ solutions). The increased opening of K+ channels appears certain to be an important cellular mechanism to vasodilation by pinacidil.

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 2466175     DOI: 10.1097/00005344-198812002-00005

Source DB:  PubMed          Journal:  J Cardiovasc Pharmacol        ISSN: 0160-2446            Impact factor:   3.105


  11 in total

Review 1.  KATP Channels in the Cardiovascular System.

Authors:  Monique N Foster; William A Coetzee
Journal:  Physiol Rev       Date:  2016-01       Impact factor: 37.312

Review 2.  Pinacidil. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in the treatment of hypertension.

Authors:  H A Friedel; R N Brogden
Journal:  Drugs       Date:  1990-06       Impact factor: 9.546

3.  Ion channel effects of pinacidil in vascular muscle.

Authors:  K Hermsmeyer
Journal:  Drugs       Date:  1988       Impact factor: 9.546

4.  Evidence that pinacidil may promote the opening of ATP-sensitive K+ channels yet inhibit the opening of Ca2(+)-activated K+ channels in K(+)-contracted canine mesenteric artery.

Authors:  K Masuzawa; T Matsuda; M Asano
Journal:  Br J Pharmacol       Date:  1990-05       Impact factor: 8.739

5.  Tissue selectivity and spasmogen selectivity of relaxant drugs in airway and pulmonary vascular smooth muscle contracted by PGF2 alpha or endothelin.

Authors:  S R O'Donnell; J C Wanstall; C S Kay; X P Zeng
Journal:  Br J Pharmacol       Date:  1991-02       Impact factor: 8.739

6.  Inhibition by the putative potassium channel opener pinacidil of the electrically-evoked release of endogenous dopamine and noradrenaline in the rat vas deferens.

Authors:  P Soares-da-Silva; M H Fernandes
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1990-10       Impact factor: 3.000

7.  Effects of pinacidil, RP 49356 and nicorandil on ATP-sensitive potassium channels in insulin-secreting cells.

Authors:  M J Dunne
Journal:  Br J Pharmacol       Date:  1990-03       Impact factor: 8.739

8.  Modulation of intracellular calcium by potassium channel openers in vascular muscle.

Authors:  P Erne; K Hermsmeyer
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1991-12       Impact factor: 3.000

9.  Potassium channel modulation in rat portal vein by ATP depletion: a comparison with the effects of levcromakalim (BRL 38227).

Authors:  T Noack; G Edwards; P Deitmer; A H Weston
Journal:  Br J Pharmacol       Date:  1992-12       Impact factor: 8.739

10.  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

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.