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PMID: 1724758 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Bay K 8644 enhances Ca2+ channel activities in embryonic chick heart cells without prolongation of open times.

European journal of pharmacology ·Vol. 203 ·No. 2 ·1991-10-15 ·Pages 307-10

Tohse N, Conforti L, Sperelakis N

Abstract

The effects of the Ca2+ channel agonist, Bay K 8644, on the slow (L-type) Ca2+ channels was examined in young (3-day-old) embryonic chick heart cells, which naturally exhibit long-lasting openings. Bay K 8644 (5 microM) increased (a) the peak amplitude of the ensemble-averaged current by 3.9 +/- 0.9-fold (mean +/- S.E.) and (b) the maximal number of simultaneous opening from 2.6 +/- 0.4 to 4.4 +/- 0.9. Bay K 8644 had no effect on the unitary conductance (27 pS in control), and relatively little effect in the open-close kinetic analysis. The mean open times were 4.2 ms and 5.2 ms, in control and Bay K 8644, respectively. These results suggest that the agonistic effect of Bay K 8644 involves a mechanism other than open-time prolongation, such as activation of silent channels.

MeSH Terms
3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester/pharmacology Animals Calcium/physiology Calcium Channels/drug effects Cells, Cultured Chick Embryo Heart/drug effects Myocardium/cytology Stimulation, Chemical
Chemicals
Calcium Channels 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester Calcium
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Tohse N
Department of Physiology and Biophysics, University of Cincinnati, College of Medicine, OH.
Conforti L
Sperelakis N
Article Info
Journal
European journal of pharmacology
Abbr.
Eur J Pharmacol
ISSN
0014-2999
Published
1991-10-15
Pages
307-10
Language
English
Region
Netherlands
NLM ID
1254354
Subset
IM
Grants
NHLBI NIH HHS · HL-31942 · United States
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