INHIBITION OF I-KS IN GUINEA-PIG CARDIAC MYOCYTES AND GUINEA-PIG I-SKCHANNELS BY THE CHROMANOL 293B

Citation
Ae. Busch et al., INHIBITION OF I-KS IN GUINEA-PIG CARDIAC MYOCYTES AND GUINEA-PIG I-SKCHANNELS BY THE CHROMANOL 293B, Pflugers Archiv, 432(6), 1996, pp. 1094-1096
Citations number
13
Categorie Soggetti
Physiology
Journal title
ISSN journal
00316768
Volume
432
Issue
6
Year of publication
1996
Pages
1094 - 1096
Database
ISI
SICI code
0031-6768(1996)432:6<1094:IOIIGC>2.0.ZU;2-W
Abstract
The chromanol derivative 293B was previously shown to inhibit a cAMP r egulated K+ conductance in rat colon crypts. Subsequent studies on clo ned K+ channels from the rat demonstrated that 293B blocks specificall y I-sK channels expressed in Xenopus oocytes, but does not affect the delayed and inward rectifier Kv1.1 and KiR2.1, respectively. In the pr esent study, the specificity of 293B for the cardiac K+ conductances I -Ks and I-Kr, and for the cloned guinea pig I-sK channel and the human HERG channel, which underly I-Ks and I-Kr, respectively, was analyzed . 293B inhibited both the slowly activating K+ conductance I-Ks in car diac myocytes and guinea pig I-sK channels expressed in Xenopus oocyte s with a similar IC50 (2-6 mu mol/l). In contrast, high concentrations of 293B had only a negligible effect on the more rapid activating I-K r. Similarly, 293B exerted no effect on HERG channels expressed in Xen opus oocytes. In summary, 293B appears to be a rather specific inhibit or of I-Ks and the underlying I-sK channels.