Genistein Directly Induces Cardiac CFTR Chloride Current by a Tyrosine Kinase-Independent and Protein Kinase A-Independent Pathway in Guinea Pig Ventricular Myocytes

1997 ◽  
Vol 235 (1) ◽  
pp. 74-78 ◽  
Author(s):  
Chern-En Chiang ◽  
Shih-Ann Chen ◽  
Mau-Song Chang ◽  
Cheng-I Lin ◽  
Hsiang-Ning Luk
2001 ◽  
Vol 441 (6) ◽  
pp. 807-815 ◽  
Author(s):  
Jens Kockskämper ◽  
Kirsty Sendhoff ◽  
Simone Erlenkamp ◽  
Frank Bordusa ◽  
Vaclav Cerovsky ◽  
...  

2000 ◽  
Vol 279 (5) ◽  
pp. H2104-H2115 ◽  
Author(s):  
Jiequan Zhu ◽  
Gregory R. Ferrier

A role for Ca2+-calmodulin-dependent kinase (CamK) in regulation of the voltage-sensitive release mechanism (VSRM) was investigated in guinea pig ventricular myocytes. Voltage clamp was used to separate the VSRM from Ca2+-induced Ca2+release (CICR). VSRM contractions and Ca2+ transients were absent in cells dialyzed with standard pipette solution but present when 2–5 μM calmodulin was included. Effects of calmodulin were blocked by KN-62 (CamK inhibitor), but not H-89, a protein kinase A (PKA) inhibitor. Ca2+ current and caffeine contractures were not affected by calmodulin. Transient-voltage relations were bell-shaped without calmodulin, but they were sigmoidal and typical of the VSRM with calmodulin. Contractions with calmodulin exhibited inactivation typical of the VSRM. These contractions were inhibited by rapid application of 200 μM of tetracaine, but not 100 μM of Cd2+, whereas CICR was inhibited by Cd2+ but not tetracaine. In undialyzed myocytes (high-resistance microelectrodes), KN-62 or H-89 each reduced amplitudes of VSRM contractions by ∼50%, but together they decreased VSRM contractions by 93%. Thus VSRM is facilitated by CamK or PKA, and both pathways regulate the VSRM in undialyzed cells.


1999 ◽  
Vol 438 (2) ◽  
pp. 205-212 ◽  
Author(s):  
D. B. Duridanova ◽  
P. S. Petkova-Kirova ◽  
L. T. Lubomirov ◽  
H. Gagov ◽  
K. Boev

2011 ◽  
Vol 31 (22) ◽  
pp. 4392-4404 ◽  
Author(s):  
S. Luz ◽  
P. Kongsuphol ◽  
A. I. Mendes ◽  
F. Romeiras ◽  
M. Sousa ◽  
...  

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