In vitro and in vivo vascular responses to the L-type calcium channel activator, Bay K 8644, in rats with cirrhosis

1998 ◽  
Vol 13 (12) ◽  
pp. 1254-1258 ◽  
Author(s):  
RICHARD MOREAU ◽  
FREDERIC OBERTI ◽  
PHILIPPE LAHAYE ◽  
ADRIAN GADANO ◽  
STEPHANE CAILMAIL ◽  
...  
1986 ◽  
Vol 64 (6) ◽  
pp. 760-763 ◽  
Author(s):  
Seymour Heisler

The dihydropyridine calcium channel activator, BAY-K-8644, stimulates cGMP formation in ACTH-secreting mouse AtT-20 clonal corticotrophs. The recent report that calmodulin antagonists could inhibit dihydropyridine binding in several tissues suggested that these agents might also affect the cyclic nucleotide response to BAY-K-8644. In fact, TMB-8, trifluoperazine, and melittin, described as in vitro antagonists of calmodulin-dependent enzyme activities, all inhibited BAY-K-8644 induced cGMP synthesis in a concentration-dependent manner. The antagonists had no effect on cGMP formation stimulated by sodium nitroprusside or sodium azide. The calcium channel antagonist, nifedipine, did not stimulate cGMP formation nor did it alter the effect of BAY-K-8644 on accumulation of the nucleotide; one explanation thus is that the cyclase involved in cGMP formation is coupled to a low affinity binding site for BAY-K-8644, which is less accessible to other dihydropyridines. The relation of cyclic GMP formation to the function of the calcium channel in AtT-20 cells remains unknown.


Endocrinology ◽  
1986 ◽  
Vol 118 (2) ◽  
pp. 545-549 ◽  
Author(s):  
CARY W. COOPER ◽  
SUSAN A. BOROSKY ◽  
PATRICK E. FARRELL ◽  
ODD S. STEINSLAND

2004 ◽  
Vol 151 (1-2) ◽  
pp. 267-276 ◽  
Author(s):  
Eun-Joo Shin ◽  
Toshitaka Nabeshima ◽  
Phil Ho Lee ◽  
Won-Ki Kim ◽  
Kwang Ho Ko ◽  
...  

1989 ◽  
Vol 160 (3) ◽  
pp. 339-347 ◽  
Author(s):  
Anne Bourson ◽  
Paul C. Moser ◽  
Alma J. Gower ◽  
Anis K. Mir

1995 ◽  
Vol 22 (2) ◽  
pp. 202-207 ◽  
Author(s):  
Marek Hartleb ◽  
Richard Moreau ◽  
Christophe Gaudin ◽  
Didier Lebrec

Sign in / Sign up

Export Citation Format

Share Document