Cromakalim-induced membrane current in guinea-pig tracheal smooth muscle cells

Citation
Y. Matsushita et al., Cromakalim-induced membrane current in guinea-pig tracheal smooth muscle cells, EUR J PHARM, 389(1), 2000, pp. 51-58
Citations number
37
Categorie Soggetti
Pharmacology & Toxicology
Journal title
EUROPEAN JOURNAL OF PHARMACOLOGY
ISSN journal
00142999 → ACNP
Volume
389
Issue
1
Year of publication
2000
Pages
51 - 58
Database
ISI
SICI code
0014-2999(20000211)389:1<51:CMCIGT>2.0.ZU;2-8
Abstract
The characteristics of the cromakalim-induced membrane current were examine d in single tracheal myocytes of the guinea-pig under voltage-clamp conditi ons. When K+ concentrations in the pipette and bathing solutions were simil ar to 140 mM, cromakalim activated a membrane current (I-crom) which was in ward at -60 mV and reversed at -2 mV. I-crom was blocked by 10 mu M glibenc lamide and potentiated when the ATP concentration in the pipette solution w as decreased. The K-d and Hill coefficient of glibenclamide for I-crom bloc k were 200 nM and 1.05, respectively. Application of the tyrosine kinase in hibitors, genistein and alpha-cyano-3-ethoxy-4-hydroxy-5-phenylthiomethylci nnamamid (ST638), reduced I-crom in a concentration-dependent manner. Daidz ein, which does not inhibit tyrosine kinase, was about 10 times less effect ive than genistein. Herbimycin A had no effect on I-crom. Internal applicat ion of these inhibitors from the pipette did not affect I-crom. In conclusi on, cromakalim is a potent activator of the ATP-sensitive K+ channel (K-ATP channel) in guinea-pig tracheal myocytes. The inhibition of I-crom by geni stein and ST638 may be due to the direct block of the channel from outside. (C) 2000 Elsevier Science B.V. All rights reserved.