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Effects of Cl- channel blockers on the cardiac ATP-sensitive K+ channel
Article de En | WPRIM | ID: wpr-728244
Bibliothèque responsable: WPRO
ABSTRACT
To explore whether Cl- channel blockers interact with the ATP-sensitive K+ (KATP) channel, I have examined the effect of two common Cl- channel blockers on the KATP channel activity in isolated rat ventricular myocytes using patch clamp techniques. In inside-out patches, 4,4'-diisothio-cyanatostilbene-2,2'-disulfonic acid (DIDS) and niflumic acid applied to bath solution inhibited the KATP channel activity in a concentration-dependent manner with IC50 of 0.24 and 927 muM, respectively. The inhibitory action of DIDS was irreversible whereas that of niflumic acid was reversible. Furthermore, DIDS-induced block was not recovered despite exposure to ATP (1 mM). In cell-attached and inside-out patches, DIDS blocked the pinacidil- or 2,4-dinitrophenol (DNP)-induced KATP channel openings. In contrast, niflumic acid did not block the pinacidil-induced KATP channel openings in inside-out patches, but inhibited it in cell-attached patches. DIDS and niflumic acid produced additional block in the presence of ATP and did not affect current-voltage relationship and channel kinetics. All these results indicate that DIDS among Cl- channel blockers specifically blocks the cardiac KATP channel.
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Texte intégral: 1 Indice: WPRIM Sujet Principal: Bains / Cinétique / Adénosine triphosphate / Acide niflumique / Acide 4,4'-diisothiocyano-stilbène-2,2'-disulfonique / Techniques de patch-clamp / 2,4-Dinitro-phénol / Concentration inhibitrice 50 / Cellules musculaires Type d'étude: Diagnostic_studies Limites du sujet: Animals langue: En Texte intégral: The Korean Journal of Physiology and Pharmacology Année: 1999 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Bains / Cinétique / Adénosine triphosphate / Acide niflumique / Acide 4,4'-diisothiocyano-stilbène-2,2'-disulfonique / Techniques de patch-clamp / 2,4-Dinitro-phénol / Concentration inhibitrice 50 / Cellules musculaires Type d'étude: Diagnostic_studies Limites du sujet: Animals langue: En Texte intégral: The Korean Journal of Physiology and Pharmacology Année: 1999 Type: Article