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Gewählte Publikation:

Quasthoff, S; Franke, C; Hatt, H; Richter-Turtur, M.
Two different types of potassium channels in human skeletal muscle activated by potassium channel openers.
Neurosci Lett. 1990; 119(2):191-194 Doi: 10.1016/0304-3940(90)90831-S
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Führende Autor*innen der Med Uni Graz
Quasthoff Stefan
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Abstract:
The inside-out patch clamp technique was used to record the effects of K+ channel openers (EMD 52692, RP 49356 and Cromakalim) on single channel currents in membrane blebs of human skeletal muscle. Two types of K+ channels were activated by these drugs: an ATP-sensitive K+ channel which was inhibited by 3 mM ATP and 5 microM Glibenclamide and an ATP insensitive K+ channel. The open probability of both types was strongly increased by K+ channel openers. Glibenclamide antagonized the action of the K+ channel openers.
Find related publications in this database (using NLM MeSH Indexing)
Adenosine Triphosphate - pharmacology
Benzopyrans - pharmacology
Cromakalim - pharmacology
Dihydropyridines - pharmacology
Electrophysiology - pharmacology
Glyburide - pharmacology
Humans - pharmacology
Muscles - metabolism
Picolines - pharmacology
Potassium Channels - drug effects
Pyrans - pharmacology
Pyrroles - pharmacology

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