Tedisamil (KC 8857) differentially inhibits the 86Rb+ efflux-stimulating and vasorelaxant properties of cromakalim-Reference-Cited by-同舟云学术

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Tedisamil (KC 8857) differentially inhibits the 86Rb+ efflux-stimulating and vasorelaxant properties of cromakalim

Published:1991-07 Issue:1 Volume:200 Page:163-165
ISSN:0014-2999
Container-title:European Journal of Pharmacology
language:en
Short-container-title:European Journal of Pharmacology

Author:

Bray Katharine,Quast Ulrich

Publisher

Elsevier BV

Subject

Pharmacology

Reference10 articles.

1. Class III antiarrhythmic actions of tedisamil (KC8857);Beatch;Eur. J. Pharmacol.,1990

2. Differential concentration-dependent effects of K-channel openers on 42K and 86Rb+ efflux in rabbit isolated aorta;Bray;Br. J. Pharmacol.,1989

3. Differences between the effects of cromakalim and nifedipine on agonist-induced responses in rabbit aorta;Bray;Br. J. Pharmacol.,1991

4. Potassium channel pharmacology;Cook,1990

5. Tedisamil inactivates transient outward K+ current in rat ventricular myocytes;Dukes;Am. J. Physiol.,1989

Cited by 17 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Tedisamil: master switch of nature?;Expert Opinion on Investigational Drugs;2001-01

2. Interaction of the diuretics torasemide and U-37883A with the KATP channel in rat isolated aorta;Naunyn-Schmiedeberg's Archives of Pharmacology;1998-08-04

3. Inhibition by protein kinase C of the 86Rb+ efflux and vasorelaxation induced by P1075, a KATP channel opener, in rat isolated aorta;Naunyn-Schmiedeberg's Archives of Pharmacology;1997-08-22

4. Activators of protein kinase A induce a glibenclamide-sensitive 86Rb+ efflux in rat isolated aorta;Naunyn-Schmiedeberg's Archives of Pharmacology;1997-03-21

5. Pharmacological characterization of the sulphonylurea receptor in rat isolated aorta;British Journal of Pharmacology;1997-01

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