Tolerance to ischemia and hypoxia is reduced in aged human myocardium

Background: Recovery of cardiac function after cardiac surgery and other interventional cardiac procedures in elderly patients is inferior to that in younger patients, suggesting that the aged myocardium is more sensitive to ischemia and other stresses. Although convincing data from animal studies o...

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Veröffentlicht in:The Journal of thoracic and cardiovascular surgery 2000-10, Vol.120 (4), p.660-667
Hauptverfasser: Mariani, Justin, Ou, Ruchong, Bailey, Michael, Rowland, Michael, Nagley, Phillip, Rosenfeldt, Franklin, Pepe, Salvatore
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container_end_page 667
container_issue 4
container_start_page 660
container_title The Journal of thoracic and cardiovascular surgery
container_volume 120
creator Mariani, Justin
Ou, Ruchong
Bailey, Michael
Rowland, Michael
Nagley, Phillip
Rosenfeldt, Franklin
Pepe, Salvatore
description Background: Recovery of cardiac function after cardiac surgery and other interventional cardiac procedures in elderly patients is inferior to that in younger patients, suggesting that the aged myocardium is more sensitive to ischemia and other stresses. Although convincing data from animal studies of senescence now exist, there is a dearth of controlled in vitro studies that examine the specific response of aged human myocardium to the stress of hypoxia or ischemia. Objective: We sought to determine the effect of age on the capacity of human atrial trabeculae to recover contractile function after in vitro hypoxic or ischemic stress. Methods: Atrial pectinate trabeculae were dissected from the tip of 58 right atrial appendages harvested during an operation in patients aged between 34 and 89 years and electrically stimulated at 1 Hz in oxygenated Ringer's solution at 37°C. Tissues experienced 30 minutes of either hypoxia (N2 and perfusate) or simulated ischemia (humidified N2 without perfusate) and were returned to normoxia for recovery of function for 30 minutes. Developed force and other contractile variables were determined during each period. Results: Under normoxic conditions, no significant age difference was observed for any contractile function variable. However, after hypoxia, the old (70-89 years) and intermediate age groups (60-69 years) showed reduced recovery of developed force (48.5% ± 22.2% [n = 11] and 44.9% ± 19% [n = 12], respectively) compared with that found (66.4% ± 19.7% [n = 15]) in the younger (34-59 years) group (mean ± SD, P = .02). Similarly, after simulated ischemia, the groups of 70- to 89-year-old and 60- to 69-year-old subjects showed reduced recovery of developed force (35.7% ± 17% [n = 5] and 51.1% ± 11.8% [n = 9], respectively) compared with that found (68.2% ± 10.4% [n = 6]) in the group of 34- to 59-year-old subjects (P = .01). Multivariable analysis, comparing 20 factors of surgical patient characteristics and recovery of developed force, found that only age (P = .01) and hypertension (P = .01) were predictors of reduced recovery of developed force after either hypoxia or simulated ischemia. Conclusions: In aged human atrial myocardium, the capacity to recover contractile function after in vitro hypoxia or simulated ischemia is reduced compared with the younger myocardium of mature adults. These findings suggest that enhanced myocardial protective strategies may be indicated for elderly patients undergoing cardiac surgery
doi_str_mv 10.1067/mtc.2000.106528
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Although convincing data from animal studies of senescence now exist, there is a dearth of controlled in vitro studies that examine the specific response of aged human myocardium to the stress of hypoxia or ischemia. Objective: We sought to determine the effect of age on the capacity of human atrial trabeculae to recover contractile function after in vitro hypoxic or ischemic stress. Methods: Atrial pectinate trabeculae were dissected from the tip of 58 right atrial appendages harvested during an operation in patients aged between 34 and 89 years and electrically stimulated at 1 Hz in oxygenated Ringer's solution at 37°C. Tissues experienced 30 minutes of either hypoxia (N2 and perfusate) or simulated ischemia (humidified N2 without perfusate) and were returned to normoxia for recovery of function for 30 minutes. Developed force and other contractile variables were determined during each period. Results: Under normoxic conditions, no significant age difference was observed for any contractile function variable. However, after hypoxia, the old (70-89 years) and intermediate age groups (60-69 years) showed reduced recovery of developed force (48.5% ± 22.2% [n = 11] and 44.9% ± 19% [n = 12], respectively) compared with that found (66.4% ± 19.7% [n = 15]) in the younger (34-59 years) group (mean ± SD, P = .02). Similarly, after simulated ischemia, the groups of 70- to 89-year-old and 60- to 69-year-old subjects showed reduced recovery of developed force (35.7% ± 17% [n = 5] and 51.1% ± 11.8% [n = 9], respectively) compared with that found (68.2% ± 10.4% [n = 6]) in the group of 34- to 59-year-old subjects (P = .01). Multivariable analysis, comparing 20 factors of surgical patient characteristics and recovery of developed force, found that only age (P = .01) and hypertension (P = .01) were predictors of reduced recovery of developed force after either hypoxia or simulated ischemia. Conclusions: In aged human atrial myocardium, the capacity to recover contractile function after in vitro hypoxia or simulated ischemia is reduced compared with the younger myocardium of mature adults. These findings suggest that enhanced myocardial protective strategies may be indicated for elderly patients undergoing cardiac surgery. 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Vascular system ; Coronary Artery Bypass ; Coronary heart disease ; Female ; Heart ; Heart Atria - physiopathology ; Humans ; Hypoxia - physiopathology ; In Vitro Techniques ; Linear Models ; Male ; Medical sciences ; Middle Aged ; Myocardial Contraction - physiology ; Myocardial Ischemia - physiopathology</subject><ispartof>The Journal of thoracic and cardiovascular surgery, 2000-10, Vol.120 (4), p.660-667</ispartof><rights>2000 American Association for Thoracic Surgery</rights><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c445t-f9856bcfd95beca199f2a894186024cc02fb552575fa9132a1e5720e2f7dfcb33</citedby><cites>FETCH-LOGICAL-c445t-f9856bcfd95beca199f2a894186024cc02fb552575fa9132a1e5720e2f7dfcb33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1067/mtc.2000.106528$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3549,27923,27924,45994</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1524080$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11003745$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mariani, Justin</creatorcontrib><creatorcontrib>Ou, Ruchong</creatorcontrib><creatorcontrib>Bailey, Michael</creatorcontrib><creatorcontrib>Rowland, Michael</creatorcontrib><creatorcontrib>Nagley, Phillip</creatorcontrib><creatorcontrib>Rosenfeldt, Franklin</creatorcontrib><creatorcontrib>Pepe, Salvatore</creatorcontrib><title>Tolerance to ischemia and hypoxia is reduced in aged human myocardium</title><title>The Journal of thoracic and cardiovascular surgery</title><addtitle>J Thorac Cardiovasc Surg</addtitle><description>Background: Recovery of cardiac function after cardiac surgery and other interventional cardiac procedures in elderly patients is inferior to that in younger patients, suggesting that the aged myocardium is more sensitive to ischemia and other stresses. Although convincing data from animal studies of senescence now exist, there is a dearth of controlled in vitro studies that examine the specific response of aged human myocardium to the stress of hypoxia or ischemia. Objective: We sought to determine the effect of age on the capacity of human atrial trabeculae to recover contractile function after in vitro hypoxic or ischemic stress. Methods: Atrial pectinate trabeculae were dissected from the tip of 58 right atrial appendages harvested during an operation in patients aged between 34 and 89 years and electrically stimulated at 1 Hz in oxygenated Ringer's solution at 37°C. Tissues experienced 30 minutes of either hypoxia (N2 and perfusate) or simulated ischemia (humidified N2 without perfusate) and were returned to normoxia for recovery of function for 30 minutes. Developed force and other contractile variables were determined during each period. Results: Under normoxic conditions, no significant age difference was observed for any contractile function variable. However, after hypoxia, the old (70-89 years) and intermediate age groups (60-69 years) showed reduced recovery of developed force (48.5% ± 22.2% [n = 11] and 44.9% ± 19% [n = 12], respectively) compared with that found (66.4% ± 19.7% [n = 15]) in the younger (34-59 years) group (mean ± SD, P = .02). Similarly, after simulated ischemia, the groups of 70- to 89-year-old and 60- to 69-year-old subjects showed reduced recovery of developed force (35.7% ± 17% [n = 5] and 51.1% ± 11.8% [n = 9], respectively) compared with that found (68.2% ± 10.4% [n = 6]) in the group of 34- to 59-year-old subjects (P = .01). Multivariable analysis, comparing 20 factors of surgical patient characteristics and recovery of developed force, found that only age (P = .01) and hypertension (P = .01) were predictors of reduced recovery of developed force after either hypoxia or simulated ischemia. Conclusions: In aged human atrial myocardium, the capacity to recover contractile function after in vitro hypoxia or simulated ischemia is reduced compared with the younger myocardium of mature adults. These findings suggest that enhanced myocardial protective strategies may be indicated for elderly patients undergoing cardiac surgery. (J Thorac Cardiovasc Surg 2000;120:660-7)</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Aging - physiology</subject><subject>Analysis of Variance</subject><subject>Biological and medical sciences</subject><subject>Cardiology. Vascular system</subject><subject>Coronary Artery Bypass</subject><subject>Coronary heart disease</subject><subject>Female</subject><subject>Heart</subject><subject>Heart Atria - physiopathology</subject><subject>Humans</subject><subject>Hypoxia - physiopathology</subject><subject>In Vitro Techniques</subject><subject>Linear Models</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Myocardial Contraction - physiology</subject><subject>Myocardial Ischemia - physiopathology</subject><issn>0022-5223</issn><issn>1097-685X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUFP3DAQRq2Kqmxpz9xQDqicAmMnTuwjQpRWQuqFSr1Zjj0mRnGy2Amw_77eZiVOPc2M9ObT6A0hpxQuKTTtVZjNJQP4N3EmPpANBdmWjeB_jsgGgLGSM1Ydk88pPWWuBSo_kWNKAaq25hty-zANGPVosJinwifTY_C60KMt-t12esu9T0VEuxi0hR8L_ZhrvwQ9FmE3GR2tX8IX8tHpIeHXQz0hv7_fPtz8KO9_3f28ub4vTV3zuXRS8KYzzkreodFUSse0kDUVDbDaGGCu45zxljstacU0Rd4yQOZa60xXVSfk25q7jdPzgmlWIZ-Mw6BHnJakWsYEr4XI4NUKmjilFNGpbfRBx52ioPbmVDan9ubUai5vnB2ily6gfecPqjJwfgB0Mnpwe2k-vXOc1SAgYxcr1vvH_tVHVCnoYcipVD3NJlEGqlZNsyflSmI29uIxqmQ85k_YvGVmZSf_32v_Ato9ln0</recordid><startdate>20001001</startdate><enddate>20001001</enddate><creator>Mariani, Justin</creator><creator>Ou, Ruchong</creator><creator>Bailey, Michael</creator><creator>Rowland, Michael</creator><creator>Nagley, Phillip</creator><creator>Rosenfeldt, Franklin</creator><creator>Pepe, Salvatore</creator><general>Mosby, Inc</general><general>AATS/WTSA</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20001001</creationdate><title>Tolerance to ischemia and hypoxia is reduced in aged human myocardium</title><author>Mariani, Justin ; Ou, Ruchong ; Bailey, Michael ; Rowland, Michael ; Nagley, Phillip ; Rosenfeldt, Franklin ; Pepe, Salvatore</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c445t-f9856bcfd95beca199f2a894186024cc02fb552575fa9132a1e5720e2f7dfcb33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Aging - physiology</topic><topic>Analysis of Variance</topic><topic>Biological and medical sciences</topic><topic>Cardiology. Vascular system</topic><topic>Coronary Artery Bypass</topic><topic>Coronary heart disease</topic><topic>Female</topic><topic>Heart</topic><topic>Heart Atria - physiopathology</topic><topic>Humans</topic><topic>Hypoxia - physiopathology</topic><topic>In Vitro Techniques</topic><topic>Linear Models</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Myocardial Contraction - physiology</topic><topic>Myocardial Ischemia - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mariani, Justin</creatorcontrib><creatorcontrib>Ou, Ruchong</creatorcontrib><creatorcontrib>Bailey, Michael</creatorcontrib><creatorcontrib>Rowland, Michael</creatorcontrib><creatorcontrib>Nagley, Phillip</creatorcontrib><creatorcontrib>Rosenfeldt, Franklin</creatorcontrib><creatorcontrib>Pepe, Salvatore</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of thoracic and cardiovascular surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mariani, Justin</au><au>Ou, Ruchong</au><au>Bailey, Michael</au><au>Rowland, Michael</au><au>Nagley, Phillip</au><au>Rosenfeldt, Franklin</au><au>Pepe, Salvatore</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tolerance to ischemia and hypoxia is reduced in aged human myocardium</atitle><jtitle>The Journal of thoracic and cardiovascular surgery</jtitle><addtitle>J Thorac Cardiovasc Surg</addtitle><date>2000-10-01</date><risdate>2000</risdate><volume>120</volume><issue>4</issue><spage>660</spage><epage>667</epage><pages>660-667</pages><issn>0022-5223</issn><eissn>1097-685X</eissn><coden>JTCSAQ</coden><abstract>Background: Recovery of cardiac function after cardiac surgery and other interventional cardiac procedures in elderly patients is inferior to that in younger patients, suggesting that the aged myocardium is more sensitive to ischemia and other stresses. Although convincing data from animal studies of senescence now exist, there is a dearth of controlled in vitro studies that examine the specific response of aged human myocardium to the stress of hypoxia or ischemia. Objective: We sought to determine the effect of age on the capacity of human atrial trabeculae to recover contractile function after in vitro hypoxic or ischemic stress. Methods: Atrial pectinate trabeculae were dissected from the tip of 58 right atrial appendages harvested during an operation in patients aged between 34 and 89 years and electrically stimulated at 1 Hz in oxygenated Ringer's solution at 37°C. Tissues experienced 30 minutes of either hypoxia (N2 and perfusate) or simulated ischemia (humidified N2 without perfusate) and were returned to normoxia for recovery of function for 30 minutes. Developed force and other contractile variables were determined during each period. Results: Under normoxic conditions, no significant age difference was observed for any contractile function variable. However, after hypoxia, the old (70-89 years) and intermediate age groups (60-69 years) showed reduced recovery of developed force (48.5% ± 22.2% [n = 11] and 44.9% ± 19% [n = 12], respectively) compared with that found (66.4% ± 19.7% [n = 15]) in the younger (34-59 years) group (mean ± SD, P = .02). Similarly, after simulated ischemia, the groups of 70- to 89-year-old and 60- to 69-year-old subjects showed reduced recovery of developed force (35.7% ± 17% [n = 5] and 51.1% ± 11.8% [n = 9], respectively) compared with that found (68.2% ± 10.4% [n = 6]) in the group of 34- to 59-year-old subjects (P = .01). Multivariable analysis, comparing 20 factors of surgical patient characteristics and recovery of developed force, found that only age (P = .01) and hypertension (P = .01) were predictors of reduced recovery of developed force after either hypoxia or simulated ischemia. Conclusions: In aged human atrial myocardium, the capacity to recover contractile function after in vitro hypoxia or simulated ischemia is reduced compared with the younger myocardium of mature adults. These findings suggest that enhanced myocardial protective strategies may be indicated for elderly patients undergoing cardiac surgery. (J Thorac Cardiovasc Surg 2000;120:660-7)</abstract><cop>Philadelphia, PA</cop><pub>Mosby, Inc</pub><pmid>11003745</pmid><doi>10.1067/mtc.2000.106528</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Aged
Aged, 80 and over
Aging - physiology
Analysis of Variance
Biological and medical sciences
Cardiology. Vascular system
Coronary Artery Bypass
Coronary heart disease
Female
Heart
Heart Atria - physiopathology
Humans
Hypoxia - physiopathology
In Vitro Techniques
Linear Models
Male
Medical sciences
Middle Aged
Myocardial Contraction - physiology
Myocardial Ischemia - physiopathology
title Tolerance to ischemia and hypoxia is reduced in aged human myocardium
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