Literature DB >> 3190749

Potassium efflux enhancement by cromakalim (BRL 34915) in rabbit mesenteric artery: an indirect effect independent of calcium?

M C Coldwell1, D R Howlett.   

Abstract

Experiments have been performed in order to investigate the calcium and exposure time dependency of cromakalim (BRL 34915)-stimulated rubidium efflux in rabbit isolated mesenteric artery. Removal of calcium from the bathing medium prolonged the effects of cromakalim on rubidium efflux. Lanthanum was without effect on cromakalim-induced efflux whilst high concentrations of nifedipine were required to produce a significant inhibitory effect. Decreasing the exposure time to cromakalim, either in the presence or absence of calcium, led to a progressive loss of the response. However, significant increases in rubidium efflux rate were observed after very short exposures (15 sec) to the drug. In normal medium, exposure to cromakalim resulted in an inhibition of a second response when the drug was reapplied. Blockade by tetraethylammonium of the initial rubidium efflux response to cromakalim did not reverse the inhibition of the second response. These results suggest that the stimulation by cromakalim of rubidium efflux in rabbit isolated mesenteric artery is independent of calcium influx and requires only a short initial exposure to the drug in order to develop a response. The development and maintenance of the response after the removal of the drug suggest that cromakalim does not directly interact with the potassium channel through which rubidium efflux enhancement is observed.

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Year:  1988        PMID: 3190749     DOI: 10.1016/0006-2952(88)90102-5

Source DB:  PubMed          Journal:  Biochem Pharmacol        ISSN: 0006-2952            Impact factor:   5.858


  6 in total

1.  Humoral and cellular effects of the K(+)-channel activator cromakalim in man.

Authors:  P Lijnen; R Fagard; J Staessen; T Weiping; E Moerman; A Amery
Journal:  Eur J Clin Pharmacol       Date:  1989       Impact factor: 2.953

2.  The novel cardioprotective agent BMS-180448 activates a potassium conductance in cardiac and vascular smooth muscle.

Authors:  N J Lodge; M A Smith
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1996-10       Impact factor: 3.000

3.  Differences in the K(+)-channels opened by cromakalim, acetylcholine and substance P in rat aorta and porcine coronary artery.

Authors:  K Bray; U Quast
Journal:  Br J Pharmacol       Date:  1991-03       Impact factor: 8.739

4.  Effect of depolarizing and hyperpolarizing agents on the membrane potential difference of primary cultures of rabbit aorta vascular smooth muscle cells.

Authors:  H Pavenstädt; V Lindeman; S Lindeman; K Kunzelmann; M Späth; R Greger
Journal:  Pflugers Arch       Date:  1991-08       Impact factor: 3.657

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

Authors:  S Duty; A H Weston
Journal:  Br J Pharmacol       Date:  1992-12       Impact factor: 8.739

6.  Potentiation of P1075-induced K+ channel opening by stimulation of adenylate cyclase in rat isolated aorta.

Authors:  C Linde; U Quast
Journal:  Br J Pharmacol       Date:  1995-06       Impact factor: 8.739

  6 in total

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