DocumentCode :
2126501
Title :
Mechanistic investigation of the causes of cellular K+ loss during acute myocardial ischemia: a simulation study
Author :
Rodriguez, B. ; Ferrero, JM, Jr.
Author_Institution :
Departamento de Ingenieria Electroncia, Univ. Politecnica de Valencia, Spain
fYear :
2001
fDate :
2001
Firstpage :
361
Lastpage :
364
Abstract :
During acute myocardial ischemia, extra-cellular K+ accumulation has been proved to induce re-entrant arrhythmias. Despite the important of this phenomenon, the causes of cellular K+ loss remain still unknown. We investigated the simultaneous effect of the activation of the ATP-sensitive K+ current [IK(ATP) ], the inhibition of the Na+/K+ pump current (INaK) and the appearance of an ischemic Na+ inward current (I0Na) on [K+]0 in the absence of coronary flow using computer modelling. Our results show that the simultaneous activation of these three mechanisms produces a fast increase of [K+]0 during the first 11.6 min, which is mainly due to the enhancement of K+ efflux. Then, [K+ ]0 stabilizes at a plateau level of 15.5 mmol/l. This biphasic time course is qualitatively and quantitatively similar to the increase of [K+]0 observed experimentally
Keywords :
cardiology; cellular transport; digital simulation; losses; medical computing; neurophysiology; physiological models; potassium; ATP-sensitive K+ current activation; K+ efflux enhancement; Na+/K+ pump current inhibition; acute myocardial ischemia; adenosine triphosphate; biphasic time course; cellular K+ loss; computer modelling; coronary flow; extra-cellular K+ accumulation; ischemic Na+ inward current; reentrant arrhythmia; simulation; stabilization; Biochemistry; Biomembranes; Cardiac tissue; Cardiology; Cells (biology); Extracellular; Ischemic pain; Myocardium; Permeability; Sugar;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Computers in Cardiology 2001
Conference_Location :
Rotterdam
ISSN :
0276-6547
Print_ISBN :
0-7803-7266-2
Type :
conf
DOI :
10.1109/CIC.2001.977667
Filename :
977667
Link To Document :
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