Potassium channel openers: pharmacological and clinical aspects

No abstract is available for this paper.

• Publication year

  1992

• Venue

  Fundamental & Clinical Pharmacology

• Publication date

  1992-10-01

• Fields of study

  Medicine, Chemistry

• Identifiers
  DOI 10.1111/j.1472-8206.1992.tb00122.xPMID 1490649
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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• Effects of a potassium channel opener (SDZ PCO 400) on guinea‐pig and human pulmonary airways

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• K+ channel openers and 'natural' cardioprotection.

  1992influential reference
• A specific binding site for K+ channel openers in rat aorta.

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• EMD 52692 (bimakalim), a new potassium channel opener, attenuates luminol-enhanced chemiluminescence and superoxide anion radical formation by zymosan-activated polymorphonuclear leukocytes.

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• Potassium Channel Openers: Pharmacology and Therapeutic Prospects

  1992influential reference
• Potassium channel openers dilate large epicardial coronary arteries in conscious dogs by an indirect, endothelium-dependent mechanism.

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• Clinical pharmacology of potassium channel openers.

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  1992cited by this paper
• Recent progress in potassium channel opener pharmacology.

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  1991cited by this paper
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• Potassium channel modulators: scientific applications and therapeutic promise.

  1990influential reference
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  1990influential reference
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  1990cited by this paper
• The action of diazoxide and minoxidil sulphate on rat blood vessels: a comparison with cromakalim

  1990cited by this paper
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  1990cited by this paper
• Hypoxic dilation of coronary arteries is mediated by ATP-sensitive potassium channels.

  1990cited by this paper
• Interrelation between pinacidil and intracellular ATP concentrations on activation of the ATP-sensitive K+ current in guinea pig ventricular myocytes.

  1990cited by this paper
• Electrophysiological actions of BRL 34915 in isolated guinea pig ventricular myocytes

  1990cited by this paper
• Two components of cardiac delayed rectifier K+ current. Differential sensitivity to block by class III antiarrhythmic agents

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• Properties and functions of ATP-sensitive K-channels.

  1990cited by this paper
• K+ channel openers activate brain sulfonylurea-sensitive K+ channels and block neurosecretion.

  1990cited by this paper
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  1990cited by this paper
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  1990cited by this paper
• Apparent competition between ATP and the potassium channel opener RP 49356 on ATP-sensitive K+ channels of cardiac myocytes.

  1989cited by this paper
• Effects of putative activators of K+ channels in mouse pancreatic β‐cells

  1989cited by this paper
• In vitro and in vivo comparison of two K+ channel openers, diazoxide and cromakalim, and their inhibition by glibenclamide.

  1989cited by this paper
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  1989cited by this paper
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  1989cited by this paper
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  1989cited by this paper
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  1989cited by this paper
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  1989cited by this paper
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  1989cited by this paper
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  1989cited by this paper
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  1988cited by this paper
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  1988cited by this paper
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  1988cited by this paper
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  1987cited by this paper
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  1981cited by this paper
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