Literature DB >> 1467840

Characteristics of the contractile response of rabbit aorta produced by cromakalim in calcium-free solution.

S Duty1, A H Weston.   

Abstract

1 The effect of potassium channel opening compounds has been investigated in the smooth muscle of rabbit aorta under Ca-free conditions. Examination of the characteristics of the response has been performed using cromakalim as the prototype compound. 2 In order of potency, Ro 31-6930, cromakalim, minoxidil sulphate and pinacidil each produced a contraction in rabbit aortic strips bathed in Ca-free MOPS-buffered physiological salt solution (PSS). In contrast, forskolin, glyceryl trinitrate and nifedipine each failed to increase tension under identical conditions. Cromakalim also evoked contraction of bovine trachealis muscle bathed in Ca-free PSS. 3. The contractile response to cromakalim in rabbit aortic strips was of delayed onset (15-20 min) and reached a plateau after approximately 120 min (1.8 g maximum with 1 microM cromakalim). No cromakalim-induced tension changes were observed in either 1 mM or 2.5 mM Ca-containing PSS. 4. Raising the [KCl] of the Ca-free PSS to 65.9 mM fully inhibited the cromakalim-induced contraction in rabbit aortic strips. In addition, pretreatment of aortic strips with the sulphonylurea glibenclamide antagonized the subsequent mechanical response to cromakalim. 5. In Ca-free PSS, cromakalim (1 microM) stimulated 42K-efflux with a time-course corresponding to the contractile event. Glibenclamide (1 microM) inhibited this cromakalim-induced 42K-efflux. 6. In sharp microelectrode studies in bovine trachealis, cromakalim (10 microM) produced a sustained membrane hyperpolarization in normal PSS. In contrast, the cromakalim-induced hyperpolarization in Ca-free PSS was not sustained. The fading of the hyperpolarization was temporally correlated with the increase in tension under these experimental conditions. 7. It is concluded that the K-channel opener-induced smooth muscle contractile response revealed in Ca-free PSS is the consequence of K-channel opening. The nature of the detailed mechanism which underlies this contractile phenomenon remains to be determined.

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Year:  1992        PMID: 1467840      PMCID: PMC1907956          DOI: 10.1111/j.1476-5381.1992.tb13428.x

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  36 in total

1.  Direct action of BRL 38227 and glibenclamide on intracellular calcium stores in cultured airway smooth muscle of rabbit.

Authors:  L C Chopra; C H Twort; J P Ward
Journal:  Br J Pharmacol       Date:  1992-02       Impact factor: 8.739

2.  Preclinical pharmacology of Ro 31-6930, a new potassium channel opener.

Authors:  P M Paciorek; D T Burden; Y M Burke; I S Cowlrick; R S Perkins; J C Taylor; J F Waterfall
Journal:  J Cardiovasc Pharmacol       Date:  1990-02       Impact factor: 3.105

3.  Electrical and mechanical effects of BRL34915 in guinea-pig isolated trachealis.

Authors:  S L Allen; J P Boyle; J Cortijo; R W Foster; G P Morgan; R C Small
Journal:  Br J Pharmacol       Date:  1986-10       Impact factor: 8.739

4.  The relaxant action of BRL 34915 in rat uterus.

Authors:  M Hollingsworth; T Amédée; D Edwards; J Mironneau; J P Savineau; R C Small; A H Weston
Journal:  Br J Pharmacol       Date:  1987-08       Impact factor: 8.739

5.  The action of procainamide and quinidine on the alpha 1-receptor-operated channels in smooth muscle cells of guinea-pig taenia caeci.

Authors:  A Den Hertog; J Van den Akker
Journal:  Eur J Pharmacol       Date:  1987-06-04       Impact factor: 4.432

6.  The potassium channel opener cromakalim (BRL 34915) activates ATP-dependent K+ channels in isolated cardiac myocytes.

Authors:  D Escande; D Thuringer; S Leguern; I Cavero
Journal:  Biochem Biophys Res Commun       Date:  1988-07-29       Impact factor: 3.575

7.  A comparison of the haemodynamic profiles of Ro 31-6930, cromakalim and nifedipine in anaesthetised normotensive rats.

Authors:  S Duty; P M Paciorek; J F Waterfall; A H Weston
Journal:  Eur J Pharmacol       Date:  1990-08-21       Impact factor: 4.432

8.  Effects of several potassium channel openers and glibenclamide on the uterus of the rat.

Authors:  I Piper; E Minshall; S J Downing; M Hollingsworth; H Sadraei
Journal:  Br J Pharmacol       Date:  1990-12       Impact factor: 8.739

9.  Cytoplasmic calcium and the relaxation of canine coronary arterial smooth muscle produced by cromakalim, pinacidil and nicorandil.

Authors:  T Yanagisawa; T Teshigawara; N Taira
Journal:  Br J Pharmacol       Date:  1990-09       Impact factor: 8.739

10.  Potassium-channel blockers inhibit inositol trisphosphate-induced calcium release in the microsomal fractions isolated from the rat brain.

Authors:  J Shah; H C Pant
Journal:  Biochem J       Date:  1988-03-01       Impact factor: 3.857

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