Evidence for mobilization of intracellular calcium during the contractile response of the rat aorta to U44069

1982 ◽  
Vol 60 (5) ◽  
pp. 743-746 ◽  
Author(s):  
Richard J. Heaslip ◽  
Ralf G. Rahwan

The aim of the present investigation was to elucidate the pharmacological mechanism by which U44069, a stable PGH2 analogue, contracts the rat aorta. The results obtained demonstrate that while the contractile effect of potassium chloride is obliterated by removal of extracellular calcium, a substantial proportion of the contractile effect of U44069 persists under these conditions. The persistent effect of U44069 under calcium-free conditions was not diminished by nifedipine (a slow calcium channel blocker) but was blocked by 2-n-butyl-3-dimethylamino-5,6-methylenedioxyindene (an intracellular calcium antagonist). These results provide experimental evidence for the proposal that U44069 contracts the aorta in the absence of extracellular calcium by mobilizing intracellular calcium.


1982 ◽  
Vol 60 (12) ◽  
pp. 1737-1737
Author(s):  
Richard J. Heaslip ◽  
Ralf G. Rahwan

On page 745, left column, the first complete sentence should read "Contractions induced by U44069 in the absence of extracellular calcium (and in the absence or the presence of nifedipine, bu-MDI, or Q-bu-MDI) were expressed as a percentage of the maximum contraction induced by U44069 alone in the presence of 2.5 mM bath calcium."On page 745, the second sentence of the Results section should read "Although tissues which had been washed in calcium-free buffer containing no EGTA contracted tonically upon exposure to 100 mM KCl to 14% of the maximum attainable contraction in the presence of extracellular calcium, tissues which had been washed in calcium-free EGTA buffers were refractory."



1994 ◽  
Vol 72 (2) ◽  
pp. 634-643 ◽  
Author(s):  
C. Luscher ◽  
J. Streit ◽  
P. Lipp ◽  
H. R. Luscher

1. The reliability of the propagation of action potentials (AP) through dorsal root ganglion (DRG) cells in embryonic slice cultures was investigated during repetitive stimulation at 1–20 Hz. Membrane potentials of DRG cells were recorded intracellularly while the axons were stimulated by an extracellular electrode. 2. In analogy to the double-pulse experiments reported previously, either one or two types of propagation failures were recorded during repetitive stimulation, depending on the cell morphology. In contrast to the double-pulse experiments, the failures appeared at longer interpulse intervals and usually only after several tens of stimuli with reliable propagation. 3. In the period with reliable propagation before the failures, a decrease in the conduction velocity and in the amplitude of the afterhyperpolarization (AHP), an increase in the total membrane conductance, and the disappearance of the action potential “shoulder” were observed. 4. The reliability of conduction during repetitive stimulation was improved by lowering the extracellular calcium concentration or by replacing the extracellular calcium by strontium. The reliability of conduction decreased by the application of cadmium, a calcium channel blocker, 4-amino pyridine, a fast potassium channel blocker, or apamin or muscarine, the blockers of calcium-dependent potassium channels. The reliability of conduction was not effected by blocking the sodium potassium pump with ouabain or by replacing extracellular sodium with lithium. 5. In the period with reliable propagation cadmium, apamin, and muscarine reduced the amplitude of the AHP. The shoulder of the action potential was more pronounced and not sensitive to repetitive stimulation when extracellular calcium was replaced by strontium. It disappeared when cadmium was applied. 6. In DRG somata changes of the intracellular Ca2+ concentration were monitored by measuring the fluorescence of the Ca2+ indicator Fluo-3 with a laser-scanning confocal microscope. During repetitive stimulation, an accumulation of intracellular calcium occurred that recovered very slowly (tens of seconds) after the AP trains. 7. Computer model simulations performed in analogy to the experimental protocols produced conduction failures during repetitive stimulation only when the calcium currents during the APs were reduced. 8. From these findings it is concluded that conduction failures during repetitive stimulation are dependent on an accumulation of intracellular calcium leading to an inactivation of calcium currents, combined with small contributions of an accumulation of extracellular potassium and a summation of slow potassium conductances.



Pharmacology ◽  
1988 ◽  
Vol 37 (6) ◽  
pp. 376-384 ◽  
Author(s):  
Craig Hartman ◽  
Mahmood H. Al-Wathiqui ◽  
Harold L. Brooks ◽  
Garrett J. Gross ◽  
David C. Warltier




1991 ◽  
Vol 6 (3) ◽  
pp. 111-124 ◽  
Author(s):  
Yasushi Kondoh ◽  
Shigenori Mizusawa ◽  
Matsutaro Murakami ◽  
Ken Nagata ◽  
Hiroyuki Nakamichi ◽  
...  


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