Cross-bridge kinetics modeled from myoplasmic [Ca2+] and LV pressure at 17{degrees}C and after 37{degrees}C and 17{degrees}C ischemia

1  Department of Biomedical Engineering, Marquette University, Milwaukee 53233; Departments of 2  Anesthesiology and 3  Physiology, 4  Cardiovascular Research Center, and 5  Department of Pulmonary Medicine and Critical Care, Medical College of Wisconsin, Milwaukee 53226; and 6  Veterans Affairs Med...

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Veröffentlicht in:American journal of physiology. Heart and circulatory physiology 2003-04, Vol.284 (4), p.H1217-H1229
Hauptverfasser: Rhodes, Samhita S, Ropella, Kristina M, Audi, Said H, Camara, Amadou K. S, Kevin, Leo G, Pagel, Paul S, Stowe, David F
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container_end_page H1229
container_issue 4
container_start_page H1217
container_title American journal of physiology. Heart and circulatory physiology
container_volume 284
creator Rhodes, Samhita S
Ropella, Kristina M
Audi, Said H
Camara, Amadou K. S
Kevin, Leo G
Pagel, Paul S
Stowe, David F
description 1  Department of Biomedical Engineering, Marquette University, Milwaukee 53233; Departments of 2  Anesthesiology and 3  Physiology, 4  Cardiovascular Research Center, and 5  Department of Pulmonary Medicine and Critical Care, Medical College of Wisconsin, Milwaukee 53226; and 6  Veterans Affairs Medical Center, Milwaukee, Wisconsin 53295 We modeled changes in contractile element kinetics derived from the cyclic relationship between myoplasmic [Ca 2+ ], measured by indo 1 fluorescence, and left ventricular pressure (LVP). We estimated model rate constants of the Ca 2+ affinity for troponin C (TnC) on actin (A) filament (TnCA) and actin and myosin (M) cross-bridge (A · M) cycling in intact guinea pig hearts during baseline 37°C perfusion and evaluated changes at 1 ) 20 min 17°C pressure, 2 ) 30-min reperfusion (RP) after 30-min 37°C global ischemia during 37°C RP, and 3 ) 30-min RP after 240-min 17°C global ischemia during 37°C RP. At 17°C perfusion versus 37°C perfusion, the model predicted: A · M binding was less sensitive; A · M dissociation was slower; Ca 2+ was less likely to bind to TnCA with A · M present; and Ca 2+ and TnCA binding was less sensitive in the absence of A · M.   Model results were consistent with a cold-induced fall in heart rate from 260 beats/min (37°C) to 33 beats/min (17°C), increased diastolic LVP, and increased phasic Ca 2+ . On RP after 37°C ischemia vs. 37°C perfusion, the model predicted the following: A · M binding was less sensitive; A · M dissociation was slower; and Ca 2+ was less likely to bind to TnCA in the absence of A · M. Model results were consistent with reduced myofilament responsiveness to [Ca 2+ ] and diastolic contracture on 37°C RP. In contrast, after cold ischemia versus 37°C perfusion, A · M association and dissociation rates, and Ca 2+ and TnCA association rates, returned to preischemic values, whereas the dissociation rate of Ca 2+ from A · M was ninefold faster. This cardiac muscle kinetic model predicted a better-restored relationship between Ca 2+ and cross-bridge function on RP after an eightfold longer period of 17°C than 37°C ischemia. indo 1; ischemia-reperfusion injury; hypothermia; isolated hearts; four-state model
doi_str_mv 10.1152/ajpheart.00816.2002
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We estimated model rate constants of the Ca 2+ affinity for troponin C (TnC) on actin (A) filament (TnCA) and actin and myosin (M) cross-bridge (A · M) cycling in intact guinea pig hearts during baseline 37°C perfusion and evaluated changes at 1 ) 20 min 17°C pressure, 2 ) 30-min reperfusion (RP) after 30-min 37°C global ischemia during 37°C RP, and 3 ) 30-min RP after 240-min 17°C global ischemia during 37°C RP. At 17°C perfusion versus 37°C perfusion, the model predicted: A · M binding was less sensitive; A · M dissociation was slower; Ca 2+ was less likely to bind to TnCA with A · M present; and Ca 2+ and TnCA binding was less sensitive in the absence of A · M.   Model results were consistent with a cold-induced fall in heart rate from 260 beats/min (37°C) to 33 beats/min (17°C), increased diastolic LVP, and increased phasic Ca 2+ . On RP after 37°C ischemia vs. 37°C perfusion, the model predicted the following: A · M binding was less sensitive; A · M dissociation was slower; and Ca 2+ was less likely to bind to TnCA in the absence of A · M. Model results were consistent with reduced myofilament responsiveness to [Ca 2+ ] and diastolic contracture on 37°C RP. In contrast, after cold ischemia versus 37°C perfusion, A · M association and dissociation rates, and Ca 2+ and TnCA association rates, returned to preischemic values, whereas the dissociation rate of Ca 2+ from A · M was ninefold faster. 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We estimated model rate constants of the Ca 2+ affinity for troponin C (TnC) on actin (A) filament (TnCA) and actin and myosin (M) cross-bridge (A · M) cycling in intact guinea pig hearts during baseline 37°C perfusion and evaluated changes at 1 ) 20 min 17°C pressure, 2 ) 30-min reperfusion (RP) after 30-min 37°C global ischemia during 37°C RP, and 3 ) 30-min RP after 240-min 17°C global ischemia during 37°C RP. At 17°C perfusion versus 37°C perfusion, the model predicted: A · M binding was less sensitive; A · M dissociation was slower; Ca 2+ was less likely to bind to TnCA with A · M present; and Ca 2+ and TnCA binding was less sensitive in the absence of A · M.   Model results were consistent with a cold-induced fall in heart rate from 260 beats/min (37°C) to 33 beats/min (17°C), increased diastolic LVP, and increased phasic Ca 2+ . On RP after 37°C ischemia vs. 37°C perfusion, the model predicted the following: A · M binding was less sensitive; A · M dissociation was slower; and Ca 2+ was less likely to bind to TnCA in the absence of A · M. Model results were consistent with reduced myofilament responsiveness to [Ca 2+ ] and diastolic contracture on 37°C RP. In contrast, after cold ischemia versus 37°C perfusion, A · M association and dissociation rates, and Ca 2+ and TnCA association rates, returned to preischemic values, whereas the dissociation rate of Ca 2+ from A · M was ninefold faster. 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We estimated model rate constants of the Ca 2+ affinity for troponin C (TnC) on actin (A) filament (TnCA) and actin and myosin (M) cross-bridge (A · M) cycling in intact guinea pig hearts during baseline 37°C perfusion and evaluated changes at 1 ) 20 min 17°C pressure, 2 ) 30-min reperfusion (RP) after 30-min 37°C global ischemia during 37°C RP, and 3 ) 30-min RP after 240-min 17°C global ischemia during 37°C RP. At 17°C perfusion versus 37°C perfusion, the model predicted: A · M binding was less sensitive; A · M dissociation was slower; Ca 2+ was less likely to bind to TnCA with A · M present; and Ca 2+ and TnCA binding was less sensitive in the absence of A · M.   Model results were consistent with a cold-induced fall in heart rate from 260 beats/min (37°C) to 33 beats/min (17°C), increased diastolic LVP, and increased phasic Ca 2+ . On RP after 37°C ischemia vs. 37°C perfusion, the model predicted the following: A · M binding was less sensitive; A · M dissociation was slower; and Ca 2+ was less likely to bind to TnCA in the absence of A · M. Model results were consistent with reduced myofilament responsiveness to [Ca 2+ ] and diastolic contracture on 37°C RP. In contrast, after cold ischemia versus 37°C perfusion, A · M association and dissociation rates, and Ca 2+ and TnCA association rates, returned to preischemic values, whereas the dissociation rate of Ca 2+ from A · M was ninefold faster. This cardiac muscle kinetic model predicted a better-restored relationship between Ca 2+ and cross-bridge function on RP after an eightfold longer period of 17°C than 37°C ischemia. indo 1; ischemia-reperfusion injury; hypothermia; isolated hearts; four-state model</abstract><pmid>12531735</pmid><doi>10.1152/ajpheart.00816.2002</doi></addata></record>
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title Cross-bridge kinetics modeled from myoplasmic [Ca2+] and LV pressure at 17{degrees}C and after 37{degrees}C and 17{degrees}C ischemia
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