<p>Nifedipine, verapamil and diltiazem partly inhibit isometric contractions induced by 1 μM PE in organ bath-mounted aortic segments. A) Contractions induced by 1 μM PE after incubating the segments with 1 to 100 nM nifedipine (n = 4); B) Ca<sup>2+</sup> channel blocker (CCB) concentration-response curves for the inhibition of contractions induced by 1 μM PE.</p
<p>Representative traces of nifedipine (A)-, verapamil (C)-, and Trp-His (E)-induced relaxation in P...
Calcium may be considered as the final intracellular messenger of excitation-contraction coupling. I...
Experiments were designed to analyze potential interactions between voltage-dependent calcium channe...
<p>Isometric contractions induced by Ca<sup>2+</sup> re-addition (+ Ca) to organ bath mounted aortic...
<p><b>A</b>. A representative trace of the tension developed in an endothelium-denuded small mesente...
Voltage-sensitive calcium channels (L-type) mediate the entry of extracellular calcium into smooth m...
The chief site of action of the calcium antagonist drugs is the slow calcium channel in two tissues:...
<p>Wire myography of CPA was carried out in physiological salt solution with vessels mounted under t...
To compare the effect of diltiazem and verapamil on the responsiveness of vascular smooth muscle to ...
The effects of R 56865, nifedipine, verapamil, diltiazem and flunarizine on K+- and NA-induced contr...
The effects of R 56865, nifedipine, verapamil, diltiazem and flunarizine on K+- and NA-induced contr...
The effects of SR 33557 on isolated cardiovascular preparations were compared to those of nifedipine...
<p>Representative experiments showing bar graphs with standard deviation error bars for the effects ...
AIM: To assess the blockade by CPU 86017 on the L-type calcium channels in the myocardium and on the...
<p>(<b>A</b>) Concentration-response curves for contractions to CaCl<sub>2</sub> (0.01–100 mM) in th...
<p>Representative traces of nifedipine (A)-, verapamil (C)-, and Trp-His (E)-induced relaxation in P...
Calcium may be considered as the final intracellular messenger of excitation-contraction coupling. I...
Experiments were designed to analyze potential interactions between voltage-dependent calcium channe...
<p>Isometric contractions induced by Ca<sup>2+</sup> re-addition (+ Ca) to organ bath mounted aortic...
<p><b>A</b>. A representative trace of the tension developed in an endothelium-denuded small mesente...
Voltage-sensitive calcium channels (L-type) mediate the entry of extracellular calcium into smooth m...
The chief site of action of the calcium antagonist drugs is the slow calcium channel in two tissues:...
<p>Wire myography of CPA was carried out in physiological salt solution with vessels mounted under t...
To compare the effect of diltiazem and verapamil on the responsiveness of vascular smooth muscle to ...
The effects of R 56865, nifedipine, verapamil, diltiazem and flunarizine on K+- and NA-induced contr...
The effects of R 56865, nifedipine, verapamil, diltiazem and flunarizine on K+- and NA-induced contr...
The effects of SR 33557 on isolated cardiovascular preparations were compared to those of nifedipine...
<p>Representative experiments showing bar graphs with standard deviation error bars for the effects ...
AIM: To assess the blockade by CPU 86017 on the L-type calcium channels in the myocardium and on the...
<p>(<b>A</b>) Concentration-response curves for contractions to CaCl<sub>2</sub> (0.01–100 mM) in th...
<p>Representative traces of nifedipine (A)-, verapamil (C)-, and Trp-His (E)-induced relaxation in P...
Calcium may be considered as the final intracellular messenger of excitation-contraction coupling. I...
Experiments were designed to analyze potential interactions between voltage-dependent calcium channe...