TY - JOUR
T1 - Lack of evidence of M-cells in porcine left ventricular myocardium
AU - Rodríguez-Sinovas, A.
AU - Cinca, Juan
AU - Tapias, Alfons
AU - Armadans, Lluís
AU - Tresànchez, Màrius
AU - Soler-Soler, J.
PY - 1997/2/1
Y1 - 1997/2/1
N2 - Objectives: The aim of this study was to analyze whether cells with long action potential duration, fast V(max), and spike-and-dome configuration (M-cells) are present in porcine left ventricular myocardium. Methods: Transmembrane action potentials (n = 505) of the left ventricle were recorded with conventional glass microelectrodes in an epicardial-endocardial direction at 2000 ms basic cycle length in 14 pigs. In 3 pigs, potentials were obtained at 1000, 2000, and 5000 ms cycle length before and after superfusion with quinidine HCl 1 μg/ml. In addition, transmembrane potentials (n = 52) were recorded in 4 dogs at 2000 ms cycle length to verify the ability of our protocol to detect M-cells. Results: In pigs, action potential duration at 90% repolarization was shorter (ANOVA, P < 0.001) and V(max) slower (P < 0.001) in the epicardium than in the other transmural sites, but there were no regional differences in resting membrane potential or in action potential amplitude. Potentials with particularly long phase 3 or with spike-and-dome configuration were not observed. All myocardial sites displayed rate dependence of action potential duration (P = 0.02) which was transmurally homogeneous and persisted after quinidine exposure. The drug did not induce afterdepolarizations. In dogs, potentials with spike-and-dome configuration, long duration, and fast V(max), like those described in M-cells, were detected in deep epicardial and midmyocardial areas. Conclusion: The porcine left ventricular myocardium shows transmural differences in action potential duration and V(max), but, unlike dogs, it lacks M-cells.
AB - Objectives: The aim of this study was to analyze whether cells with long action potential duration, fast V(max), and spike-and-dome configuration (M-cells) are present in porcine left ventricular myocardium. Methods: Transmembrane action potentials (n = 505) of the left ventricle were recorded with conventional glass microelectrodes in an epicardial-endocardial direction at 2000 ms basic cycle length in 14 pigs. In 3 pigs, potentials were obtained at 1000, 2000, and 5000 ms cycle length before and after superfusion with quinidine HCl 1 μg/ml. In addition, transmembrane potentials (n = 52) were recorded in 4 dogs at 2000 ms cycle length to verify the ability of our protocol to detect M-cells. Results: In pigs, action potential duration at 90% repolarization was shorter (ANOVA, P < 0.001) and V(max) slower (P < 0.001) in the epicardium than in the other transmural sites, but there were no regional differences in resting membrane potential or in action potential amplitude. Potentials with particularly long phase 3 or with spike-and-dome configuration were not observed. All myocardial sites displayed rate dependence of action potential duration (P = 0.02) which was transmurally homogeneous and persisted after quinidine exposure. The drug did not induce afterdepolarizations. In dogs, potentials with spike-and-dome configuration, long duration, and fast V(max), like those described in M-cells, were detected in deep epicardial and midmyocardial areas. Conclusion: The porcine left ventricular myocardium shows transmural differences in action potential duration and V(max), but, unlike dogs, it lacks M-cells.
KW - M-cells
KW - dog, ventricle
KW - membrane potential
KW - pig, ventricle
KW - quinidine
UR - https://www.scopus.com/pages/publications/0031015666
U2 - 10.1016/S0008-6363(96)00205-2
DO - 10.1016/S0008-6363(96)00205-2
M3 - Article
SN - 0008-6363
VL - 33
SP - 307
EP - 313
JO - Cardiovascular Research
JF - Cardiovascular Research
ER -