Developmental differences in L-type calcium current of human atrial myocytes

2004 ◽  
Vol 286 (5) ◽  
pp. H1963-H1969 ◽  
Author(s):  
Srinivas M. Tipparaju ◽  
Rajiv Kumar ◽  
Yanggan Wang ◽  
Ronald W. Joyner ◽  
Mary B. Wagner

We investigated differences in L-type Ca2+ current ( ICa) between infant (INF, 1–12 mo old), young adult (YAD, 14–18 yr old), and older adult (AD) myocytes from biopsies of right atrial appendages. Basal ICa was smaller in INF myocytes (1.2 ± 0.1 pA/pF, n = 29, 6 ± 1 mo old, 11 patients) than in YAD (2.5 ± 0.2 pA/pF, n = 20, 16 ± 1 yr old, 5 patients) or AD (2.6 ± 0.3 pA/pF, n = 19, 66 ± 3 yr old, 9 patients) myocytes ( P < 0.05). Maximal ICa produced by isoproterenol (Iso) was similar in INF, YAD, and AD cells: 8.4 ± 1.1, 9.6 ± 1.0, and 9.2 ± 1.3 pA/pF, respectively. Efficacy (Emax) was larger in INF (607 ± 50%) than for YAD (371 ± 29%) or AD (455 ± 12%) myocytes. Potency (EC50) was 8- to 10-fold higher in AD (0.82 ± 0.09 nM) or YAD (0.41 ± 0.14 nM) than in INF (7.6 ± 3.5 nM) myocytes. Protein levels were similar for Giα2 but much greater for Giα3 in INF than in AD or YAD atrial tissue. When Giα3 activity was inhibited by inclusion of a Giα3 COOH-terminal decapeptide in the pipette, basal ICa and the response to 10 nM Iso were increased in INF, but not in YAD, cells. We propose that basal ICa and the response to low-dose β-adrenergic stimulation are inhibited in INF (but not YAD or AD) cells as a result of constitutive inhibitory effects of Giα3.

1996 ◽  
Vol 27 (2) ◽  
pp. 96
Author(s):  
Theresa P. Roca ◽  
John D. Pigott ◽  
Craig W. Clarkson ◽  
Arthur S. Pickoff ◽  
William J. Crumb

2018 ◽  
Vol 314 (5) ◽  
pp. H895-H916 ◽  
Author(s):  
Anna Muszkiewicz ◽  
Xing Liu ◽  
Alfonso Bueno-Orovio ◽  
Brodie A. J. Lawson ◽  
Kevin Burrage ◽  
...  

Variability refers to differences in physiological function between individuals, which may translate into different disease susceptibility and treatment efficacy. Experiments in human cardiomyocytes face wide variability and restricted tissue access; under these conditions, computational models are a useful complementary tool. We conducted a computational and experimental investigation in cardiomyocytes isolated from samples of the right atrial appendage of patients undergoing cardiac surgery to evaluate the impact of variability in action potentials (APs) and subcellular ionic densities on Ca2+ transient dynamics. Results showed that 1) variability in APs and ionic densities is large, even within an apparently homogenous patient cohort, and translates into ±100% variation in ionic conductances; 2) experimentally calibrated populations of models with wide variations in ionic densities yield APs overlapping with those obtained experimentally, even if AP characteristics of the original generic model differed significantly from experimental APs; 3) model calibration with AP recordings restricts the variability in ionic densities affecting upstroke and resting potential, but redundancy in repolarization currents admits substantial variability in ionic densities; and 4) model populations constrained with experimental APs and ionic densities exhibit three Ca2+ transient phenotypes, differing in intracellular Ca2+ handling and Na+/Ca2+ membrane extrusion. These findings advance our understanding of the impact of variability in human atrial electrophysiology. NEW & NOTEWORTHY Variability in human atrial electrophysiology is investigated by integrating for the first time cellular-level and ion channel recordings in computational electrophysiological models. Ion channel calibration restricts current densities but not cellular phenotypic variability. Reduced Na+/Ca2+ exchanger is identified as a primary mechanism underlying diastolic Ca2+ fluctuations in human atrial myocytes.


1997 ◽  
Vol 99 (11) ◽  
pp. 2710-2718 ◽  
Author(s):  
M Rivet-Bastide ◽  
G Vandecasteele ◽  
S Hatem ◽  
I Verde ◽  
A Bénardeau ◽  
...  

1995 ◽  
Vol 95 (2) ◽  
pp. 794-802 ◽  
Author(s):  
M Kirstein ◽  
M Rivet-Bastide ◽  
S Hatem ◽  
A Bénardeau ◽  
J J Mercadier ◽  
...  

2014 ◽  
Vol 7 (5) ◽  
pp. 861-868 ◽  
Author(s):  
Adriana Barana ◽  
Marcos Matamoros ◽  
Pablo Dolz-Gaitón ◽  
Marta Pérez-Hernández ◽  
Irene Amorós ◽  
...  

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