Ca$^2+$ transients measured in failing human ventricular myocytes
exhibit reduced amplitude, slowed relaxation, and blunted frequency
dependence. In the companion article (O'Rourke B, Kass DA, Tomaselli
GF, K��b S, Tunin R, Marb�n E. Mechanisms of altered excitation-contraction
coupling in canine tachycardia-induced heart, I: experimental studies.
Circ. Res.. 1999;84:562-570), O'Rourke et al show that Ca$^2+$
transients recorded in myocytes isolated from canine hearts subjected
to the tachycardia pacing protocol exhibit similar responses. Analyses
of protein levels in these failing hearts reveal that both SR Ca$^2+$
ATPase and phospholamban are decreased on average by 28\% and that
Na$^+$/Ca$^2+$ exchanger (NCX) protein is increased on average
by 104\%. In this article, we present a model of the canine midmyocardial
ventricular action potential and Ca$^2+$ transient. The model
is used to estimate the degree of functional upregulation and downregulation
of NCX and SR Ca$^2+$ ATPase in heart failure using data obtained
from 2 different experimental protocols. Model estimates of average
SR Ca$^2+$ ATPase functional downregulation obtained using these
experimental protocols are 49\% and 62\%. Model estimates of average
NCX functional upregulation range are 38\% and 75\%. Simulation of
voltage-clamp Ca$^2+$ transients indicates that such changes
are sufficient to account for the reduced amplitude, altered shape,
and slowed relaxation of Ca$^2+$ transients in the failing canine
heart. Model analyses also suggest that altered expression of Ca$^2+$
handling proteins plays a significant role in prolongation of action
potential duration in failing canine myocytes.
%0 Journal Article
%1 Wins_1999_571
%A Winslow, R. L.
%A Rice, J.
%A Jafri, S.
%A Marb�n, E.
%A O'Rourke, B.
%D 1999
%J Circ. Res.
%K 10082479 20th ATPase, Acids, Action Animals, Antigens, Apoptosis, Blockers, CD8, CHO Calcium Calcium, California, Cardiovascular, Cell Cells, Century, Channel Channels, Congestive, Contraction, Cultured, Decanoic Diazoxide, Dinucleoside Diuretics, Dogs, Electrophysiology, Emergency Enzyme Exchanger, Factors, Failure, Flavoproteins, Forecasting, Fractions, Fusion, Gating, Glyburide, Gov't, Guinea Hamsters, Health Heart Heart, History, Humans, Hydroxy Inhibitors, Intracellular Inwardly Ion Ischemia, Ischemic Medical Membrane Membranes, Mice, Mitochondria, Models, Myocardial Myocardial, Myocardium, National Non-P.H.S., Non-U.S. P.H.S., Patch-Clamp Phosphates, Pigs, Potassium Potentials, Preconditioning, Programs, Proteins, Rabbits, Rats, Rectifying, Regional Research Reticulum, Sarcolemma, Sarcoplasmic Services, Sodium, Sodium-Calcium States, Subcellular Support, Techniques, Thiazide, Time U.S. United Voltage-Gated, {C}a$^{2+}$-Transporting
%N 5
%P 571--586
%T Mechanisms of altered excitation-contraction coupling in canine tachycardia-induced
heart failure, II: model studies.
%U http://circres.ahajournals.org/cgi/content/full/84/5/571
%V 84
%X Ca$^2+$ transients measured in failing human ventricular myocytes
exhibit reduced amplitude, slowed relaxation, and blunted frequency
dependence. In the companion article (O'Rourke B, Kass DA, Tomaselli
GF, K��b S, Tunin R, Marb�n E. Mechanisms of altered excitation-contraction
coupling in canine tachycardia-induced heart, I: experimental studies.
Circ. Res.. 1999;84:562-570), O'Rourke et al show that Ca$^2+$
transients recorded in myocytes isolated from canine hearts subjected
to the tachycardia pacing protocol exhibit similar responses. Analyses
of protein levels in these failing hearts reveal that both SR Ca$^2+$
ATPase and phospholamban are decreased on average by 28\% and that
Na$^+$/Ca$^2+$ exchanger (NCX) protein is increased on average
by 104\%. In this article, we present a model of the canine midmyocardial
ventricular action potential and Ca$^2+$ transient. The model
is used to estimate the degree of functional upregulation and downregulation
of NCX and SR Ca$^2+$ ATPase in heart failure using data obtained
from 2 different experimental protocols. Model estimates of average
SR Ca$^2+$ ATPase functional downregulation obtained using these
experimental protocols are 49\% and 62\%. Model estimates of average
NCX functional upregulation range are 38\% and 75\%. Simulation of
voltage-clamp Ca$^2+$ transients indicates that such changes
are sufficient to account for the reduced amplitude, altered shape,
and slowed relaxation of Ca$^2+$ transients in the failing canine
heart. Model analyses also suggest that altered expression of Ca$^2+$
handling proteins plays a significant role in prolongation of action
potential duration in failing canine myocytes.
@article{Wins_1999_571,
abstract = {{C}a$^{2+}$ transients measured in failing human ventricular myocytes
exhibit reduced amplitude, slowed relaxation, and blunted frequency
dependence. In the companion article (O'Rourke B, Kass {DA}, Tomaselli
{GF}, K��b S, Tunin R, Marb�n E. Mechanisms of altered excitation-contraction
coupling in canine tachycardia-induced heart, I: experimental studies.
Circ. Res.. 1999;84:562-570), O'Rourke et al show that {C}a$^{2+}$
transients recorded in myocytes isolated from canine hearts subjected
to the tachycardia pacing protocol exhibit similar responses. Analyses
of protein levels in these failing hearts reveal that both SR {C}a$^{2+}$
ATPase and phospholamban are decreased on average by 28\% and that
{N}a$^{+}$/{C}a$^{2+}$ exchanger (NCX) protein is increased on average
by 104\%. In this article, we present a model of the canine midmyocardial
ventricular action potential and {C}a$^{2+}$ transient. The model
is used to estimate the degree of functional upregulation and downregulation
of NCX and SR {C}a$^{2+}$ ATPase in heart failure using data obtained
from 2 different experimental protocols. Model estimates of average
SR {C}a$^{2+}$ ATPase functional downregulation obtained using these
experimental protocols are 49\% and 62\%. Model estimates of average
NCX functional upregulation range are 38\% and 75\%. Simulation of
voltage-clamp {C}a$^{2+}$ transients indicates that such changes
are sufficient to account for the reduced amplitude, altered shape,
and slowed relaxation of {C}a$^{2+}$ transients in the failing canine
heart. Model analyses also suggest that altered expression of {C}a$^{2+}$
handling proteins plays a significant role in prolongation of action
potential duration in failing canine myocytes.},
added-at = {2009-06-03T11:20:58.000+0200},
author = {Winslow, R. L. and Rice, J. and Jafri, S. and Marb�n, E. and O'Rourke, B.},
biburl = {https://www.bibsonomy.org/bibtex/235b91ae6be07c397522b3d49a55160c7/hake},
description = {The whole bibliography file I use.},
file = {Wins_1999_571.pdf:Wins_1999_571.pdf:PDF},
interhash = {1b2e07d0a304f81b8c6d7fddee421230},
intrahash = {35b91ae6be07c397522b3d49a55160c7},
journal = {Circ. Res.},
key = 1,
keywords = {10082479 20th ATPase, Acids, Action Animals, Antigens, Apoptosis, Blockers, CD8, CHO Calcium Calcium, California, Cardiovascular, Cell Cells, Century, Channel Channels, Congestive, Contraction, Cultured, Decanoic Diazoxide, Dinucleoside Diuretics, Dogs, Electrophysiology, Emergency Enzyme Exchanger, Factors, Failure, Flavoproteins, Forecasting, Fractions, Fusion, Gating, Glyburide, Gov't, Guinea Hamsters, Health Heart Heart, History, Humans, Hydroxy Inhibitors, Intracellular Inwardly Ion Ischemia, Ischemic Medical Membrane Membranes, Mice, Mitochondria, Models, Myocardial Myocardial, Myocardium, National Non-P.H.S., Non-U.S. P.H.S., Patch-Clamp Phosphates, Pigs, Potassium Potentials, Preconditioning, Programs, Proteins, Rabbits, Rats, Rectifying, Regional Research Reticulum, Sarcolemma, Sarcoplasmic Services, Sodium, Sodium-Calcium States, Subcellular Support, Techniques, Thiazide, Time U.S. United Voltage-Gated, {C}a$^{2+}$-Transporting},
month = Mar,
number = 5,
pages = {571--586},
pmid = {10082479},
timestamp = {2009-06-03T11:21:37.000+0200},
title = {Mechanisms of altered excitation-contraction coupling in canine tachycardia-induced
heart failure, II: model studies.},
url = {http://circres.ahajournals.org/cgi/content/full/84/5/571},
volume = 84,
year = 1999
}