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 |
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container_title | American journal of physiology. Heart and circulatory physiology |
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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 |
format | Article |
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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</description><identifier>ISSN: 0363-6135</identifier><identifier>EISSN: 1522-1539</identifier><identifier>DOI: 10.1152/ajpheart.00816.2002</identifier><identifier>PMID: 12531735</identifier><language>eng</language><ispartof>American journal of physiology. Heart and circulatory physiology, 2003-04, Vol.284 (4), p.H1217-H1229</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c254t-17c50b78a63add164b68b42479ce895f791c096efb05e4a0fb004a668ee51e643</citedby><cites>FETCH-LOGICAL-c254t-17c50b78a63add164b68b42479ce895f791c096efb05e4a0fb004a668ee51e643</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3026,27903,27904</link.rule.ids></links><search><creatorcontrib>Rhodes, Samhita S</creatorcontrib><creatorcontrib>Ropella, Kristina M</creatorcontrib><creatorcontrib>Audi, Said H</creatorcontrib><creatorcontrib>Camara, Amadou K. S</creatorcontrib><creatorcontrib>Kevin, Leo G</creatorcontrib><creatorcontrib>Pagel, Paul S</creatorcontrib><creatorcontrib>Stowe, David F</creatorcontrib><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</title><title>American journal of physiology. Heart and circulatory physiology</title><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</description><issn>0363-6135</issn><issn>1522-1539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNp1kE1Lw0AQhhdRtFZ_gZe9S9r9ToInCdYKBS_qRWTZJJNmNWnCbooW8ej_Nq3fgqcX5p1nYB6EjigZUSrZ2Ny3JRjXjQiJqBoxQtgWGvQNC6jk8TYaEK54oCiXe2jf-3tCiAwV30V7lElOQy4H6DVxjfdB6mw-B_xgF9DZzOO6yaGCHBeuqXG9atrK-Npm-DYx7PgOm0WOZze4deD90gE2Habhcw5zB-Bfkk1vig4c5n_Hv_asz0qorTlAO4WpPBx-5BBdT86ukmkwuzy_SE5nQcak6AIaZpKkYWQUN3lOlUhVlAomwjiDKJZFGNOMxAqKlEgQhvRJhFEqApAUlOBDxN_vZuuvHRS6dbY2bqUp0Wup-lOq3kjVa6k9NX6nSjsvH60D3ZYrb5uqma--ARYJLfSUsl7sEJ38T0yWVXUFT90X-oPUbV7wN5CtknI</recordid><startdate>20030401</startdate><enddate>20030401</enddate><creator>Rhodes, Samhita S</creator><creator>Ropella, Kristina M</creator><creator>Audi, Said H</creator><creator>Camara, Amadou K. S</creator><creator>Kevin, Leo G</creator><creator>Pagel, Paul S</creator><creator>Stowe, David F</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20030401</creationdate><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</title><author>Rhodes, Samhita S ; Ropella, Kristina M ; Audi, Said H ; Camara, Amadou K. S ; Kevin, Leo G ; Pagel, Paul S ; Stowe, David F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c254t-17c50b78a63add164b68b42479ce895f791c096efb05e4a0fb004a668ee51e643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rhodes, Samhita S</creatorcontrib><creatorcontrib>Ropella, Kristina M</creatorcontrib><creatorcontrib>Audi, Said H</creatorcontrib><creatorcontrib>Camara, Amadou K. S</creatorcontrib><creatorcontrib>Kevin, Leo G</creatorcontrib><creatorcontrib>Pagel, Paul S</creatorcontrib><creatorcontrib>Stowe, David F</creatorcontrib><collection>CrossRef</collection><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rhodes, Samhita S</au><au>Ropella, Kristina M</au><au>Audi, Said H</au><au>Camara, Amadou K. S</au><au>Kevin, Leo G</au><au>Pagel, Paul S</au><au>Stowe, David F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cross-bridge kinetics modeled from myoplasmic [Ca2+] and LV pressure at 17{degrees}C and after 37{degrees}C and 17{degrees}C ischemia</atitle><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle><date>2003-04-01</date><risdate>2003</risdate><volume>284</volume><issue>4</issue><spage>H1217</spage><epage>H1229</epage><pages>H1217-H1229</pages><issn>0363-6135</issn><eissn>1522-1539</eissn><abstract>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</abstract><pmid>12531735</pmid><doi>10.1152/ajpheart.00816.2002</doi></addata></record> |
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identifier | ISSN: 0363-6135 |
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source | American Physiological Society; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
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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