The Role of Glycolysis in Myocardial Calcium Control
Because glycolysis is thought to be important for maintenance of cellular ion homeostasis, the aim of the present study was to examine the role of glycolysis in the control of cytosolic calcium ([Ca2+]i) and cell shortening during conditions of increased calcium influx. Thus, [Ca2+]iand unloaded cel...
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| Veröffentlicht in: | Journal of molecular and cellular cardiology 1998-09, Vol.30 (9), p.1703-1712 |
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| creator | Aasum, Ellen Lathrop, David A Henden, Thale Sundset, Rune Larsen, Terje S. |
| description | Because glycolysis is thought to be important for maintenance of cellular ion homeostasis, the aim of the present study was to examine the role of glycolysis in the control of cytosolic calcium ([Ca2+]i) and cell shortening during conditions of increased calcium influx. Thus, [Ca2+]iand unloaded cell shortening were measured in fura-2/AM loaded rat ventricular myocytes. All cells were superfused with Tyrode's solution containing glucose and pyruvate (to preserve oxidative metabolism), and glycolysis was inhibited by iodoacetate (IAA, 100μm). Calcium influx was increased, secondary to an increase in intracellular sodium, by addition of veratrine (1μg/ml), or directly by either elevating [Ca2+]ofrom 2 to 5 mmor by exposing the cells to isoproterenol (1 to 100 nm). Veratrine exposure caused a time-dependent increase in both diastolic and systolic [Ca2+]ithat resulted in cellular calcium overload and hypercontraction. The rate of increase in [Ca2+]iwas more rapid in IAA-treated than in untreated myocytes, leading to a 13±3v5±2% increase (P |
| doi_str_mv | 10.1006/jmcc.1998.0732 |
| format | Article |
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Thus, [Ca2+]iand unloaded cell shortening were measured in fura-2/AM loaded rat ventricular myocytes. All cells were superfused with Tyrode's solution containing glucose and pyruvate (to preserve oxidative metabolism), and glycolysis was inhibited by iodoacetate (IAA, 100μm). Calcium influx was increased, secondary to an increase in intracellular sodium, by addition of veratrine (1μg/ml), or directly by either elevating [Ca2+]ofrom 2 to 5 mmor by exposing the cells to isoproterenol (1 to 100 nm). Veratrine exposure caused a time-dependent increase in both diastolic and systolic [Ca2+]ithat resulted in cellular calcium overload and hypercontraction. The rate of increase in [Ca2+]iwas more rapid in IAA-treated than in untreated myocytes, leading to a 13±3v5±2% increase (P<0.05) in diastolic [Ca2+]iafter 5 min of exposure. The corresponding increases in systolic [Ca2+]iwere 43±6 and 24±5% (P<0.05). Elevated [Ca2+]oresulted in increased [Ca2+]itransient amplitudes and cell shortening. These responses were each attenuated by inhibiting glycolysis, so that the increase was 38±5v68±9% ([Ca2+]itransient amplitude,P<0.05) and 41±11v91±18% (cell shortening,P<0.05). Inhibition of glycolysis did not, however, affect the increase in calcium transient or cell shortening during addition of isoproterenol. We conclude that glycolysis plays an essential role in the maintenance of intracellular calcium homeostasis during severe calcium overload. Glycolysis was also essential for signalling the inotropic effect that accompanied elevation in extracellular calcium, while the changes in intracellular calcium following administration of isoproterenol were not influenced by glycolysis in the present model.</description><identifier>ISSN: 0022-2828</identifier><identifier>EISSN: 1095-8584</identifier><identifier>DOI: 10.1006/jmcc.1998.0732</identifier><identifier>PMID: 9769226</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adenosine triphosphate metabolism ; Adrenergic beta-Agonists - pharmacology ; Animals ; Calcium - physiology ; Calcium Channels - drug effects ; Calcium Channels - metabolism ; Calcium homeostasis ; Calcium influx ; Fura-2 ; Glucose metabolism ; Glycolysis ; Glycolysis - physiology ; Heart - drug effects ; Heart - physiology ; Homeostasis - drug effects ; Inotropic stimuli ; Iodoacetate ; Iodoacetates - pharmacology ; Isoproterenol ; Isoproterenol - pharmacology ; Male ; Microscopy, Fluorescence ; Rat ; Rats ; Rats, Sprague-Dawley ; Ventricular cell ; Veratrine ; Veratrine - pharmacology</subject><ispartof>Journal of molecular and cellular cardiology, 1998-09, Vol.30 (9), p.1703-1712</ispartof><rights>1998 Academic Press</rights><rights>Copyright 1998 Academic Press.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c339t-a487707d410f1e7d3e5aba262aee6ea16e401846b153232e1f033c6a957ae6523</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1006/jmcc.1998.0732$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9769226$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aasum, Ellen</creatorcontrib><creatorcontrib>Lathrop, David A</creatorcontrib><creatorcontrib>Henden, Thale</creatorcontrib><creatorcontrib>Sundset, Rune</creatorcontrib><creatorcontrib>Larsen, Terje S.</creatorcontrib><title>The Role of Glycolysis in Myocardial Calcium Control</title><title>Journal of molecular and cellular cardiology</title><addtitle>J Mol Cell Cardiol</addtitle><description>Because glycolysis is thought to be important for maintenance of cellular ion homeostasis, the aim of the present study was to examine the role of glycolysis in the control of cytosolic calcium ([Ca2+]i) and cell shortening during conditions of increased calcium influx. Thus, [Ca2+]iand unloaded cell shortening were measured in fura-2/AM loaded rat ventricular myocytes. All cells were superfused with Tyrode's solution containing glucose and pyruvate (to preserve oxidative metabolism), and glycolysis was inhibited by iodoacetate (IAA, 100μm). Calcium influx was increased, secondary to an increase in intracellular sodium, by addition of veratrine (1μg/ml), or directly by either elevating [Ca2+]ofrom 2 to 5 mmor by exposing the cells to isoproterenol (1 to 100 nm). Veratrine exposure caused a time-dependent increase in both diastolic and systolic [Ca2+]ithat resulted in cellular calcium overload and hypercontraction. The rate of increase in [Ca2+]iwas more rapid in IAA-treated than in untreated myocytes, leading to a 13±3v5±2% increase (P<0.05) in diastolic [Ca2+]iafter 5 min of exposure. The corresponding increases in systolic [Ca2+]iwere 43±6 and 24±5% (P<0.05). Elevated [Ca2+]oresulted in increased [Ca2+]itransient amplitudes and cell shortening. These responses were each attenuated by inhibiting glycolysis, so that the increase was 38±5v68±9% ([Ca2+]itransient amplitude,P<0.05) and 41±11v91±18% (cell shortening,P<0.05). Inhibition of glycolysis did not, however, affect the increase in calcium transient or cell shortening during addition of isoproterenol. We conclude that glycolysis plays an essential role in the maintenance of intracellular calcium homeostasis during severe calcium overload. Glycolysis was also essential for signalling the inotropic effect that accompanied elevation in extracellular calcium, while the changes in intracellular calcium following administration of isoproterenol were not influenced by glycolysis in the present model.</description><subject>Adenosine triphosphate metabolism</subject><subject>Adrenergic beta-Agonists - pharmacology</subject><subject>Animals</subject><subject>Calcium - physiology</subject><subject>Calcium Channels - drug effects</subject><subject>Calcium Channels - metabolism</subject><subject>Calcium homeostasis</subject><subject>Calcium influx</subject><subject>Fura-2</subject><subject>Glucose metabolism</subject><subject>Glycolysis</subject><subject>Glycolysis - physiology</subject><subject>Heart - drug effects</subject><subject>Heart - physiology</subject><subject>Homeostasis - drug effects</subject><subject>Inotropic stimuli</subject><subject>Iodoacetate</subject><subject>Iodoacetates - pharmacology</subject><subject>Isoproterenol</subject><subject>Isoproterenol - pharmacology</subject><subject>Male</subject><subject>Microscopy, Fluorescence</subject><subject>Rat</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Ventricular cell</subject><subject>Veratrine</subject><subject>Veratrine - pharmacology</subject><issn>0022-2828</issn><issn>1095-8584</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM9LwzAYhoMoc06v3oSevLXmV9PmKEWnMBFknkOWfsWMtJlJK_S_t2XDm6fv8L7vA9-D0C3BGcFYPOxbYzIiZZnhgtEztCRY5mmZl_wcLTGmNKUlLS_RVYx7jLHkjC3QQhZCUiqWiG-_IPnwDhLfJGs3Gu_GaGNiu-Rt9EaH2mqXVNoZO7RJ5bs-eHeNLhrtItyc7gp9Pj9tq5d0875-rR43qWFM9qnmZVHgouYENwSKmkGud5oKqgEEaCKAY1JysSM5o4wCaTBjRmiZFxpETtkK3R-5h-C_B4i9am004JzuwA9RCSkLzAWbitmxaIKPMUCjDsG2OoyKYDVrUrMmNWtSs6ZpcHciD7sW6r_6ycuUl8ccpvd-LAQVjYXOQG0DmF7V3v6H_gUlaHTj</recordid><startdate>19980901</startdate><enddate>19980901</enddate><creator>Aasum, Ellen</creator><creator>Lathrop, David A</creator><creator>Henden, Thale</creator><creator>Sundset, Rune</creator><creator>Larsen, Terje S.</creator><general>Elsevier Ltd</general><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>19980901</creationdate><title>The Role of Glycolysis in Myocardial Calcium Control</title><author>Aasum, Ellen ; Lathrop, David A ; Henden, Thale ; Sundset, Rune ; Larsen, Terje S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c339t-a487707d410f1e7d3e5aba262aee6ea16e401846b153232e1f033c6a957ae6523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Adenosine triphosphate metabolism</topic><topic>Adrenergic beta-Agonists - pharmacology</topic><topic>Animals</topic><topic>Calcium - physiology</topic><topic>Calcium Channels - drug effects</topic><topic>Calcium Channels - metabolism</topic><topic>Calcium homeostasis</topic><topic>Calcium influx</topic><topic>Fura-2</topic><topic>Glucose metabolism</topic><topic>Glycolysis</topic><topic>Glycolysis - physiology</topic><topic>Heart - drug effects</topic><topic>Heart - physiology</topic><topic>Homeostasis - drug effects</topic><topic>Inotropic stimuli</topic><topic>Iodoacetate</topic><topic>Iodoacetates - pharmacology</topic><topic>Isoproterenol</topic><topic>Isoproterenol - pharmacology</topic><topic>Male</topic><topic>Microscopy, Fluorescence</topic><topic>Rat</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Ventricular cell</topic><topic>Veratrine</topic><topic>Veratrine - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aasum, Ellen</creatorcontrib><creatorcontrib>Lathrop, David A</creatorcontrib><creatorcontrib>Henden, Thale</creatorcontrib><creatorcontrib>Sundset, Rune</creatorcontrib><creatorcontrib>Larsen, Terje S.</creatorcontrib><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>Journal of molecular and cellular cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aasum, Ellen</au><au>Lathrop, David A</au><au>Henden, Thale</au><au>Sundset, Rune</au><au>Larsen, Terje S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Role of Glycolysis in Myocardial Calcium Control</atitle><jtitle>Journal of molecular and cellular cardiology</jtitle><addtitle>J Mol Cell Cardiol</addtitle><date>1998-09-01</date><risdate>1998</risdate><volume>30</volume><issue>9</issue><spage>1703</spage><epage>1712</epage><pages>1703-1712</pages><issn>0022-2828</issn><eissn>1095-8584</eissn><abstract>Because glycolysis is thought to be important for maintenance of cellular ion homeostasis, the aim of the present study was to examine the role of glycolysis in the control of cytosolic calcium ([Ca2+]i) and cell shortening during conditions of increased calcium influx. Thus, [Ca2+]iand unloaded cell shortening were measured in fura-2/AM loaded rat ventricular myocytes. All cells were superfused with Tyrode's solution containing glucose and pyruvate (to preserve oxidative metabolism), and glycolysis was inhibited by iodoacetate (IAA, 100μm). Calcium influx was increased, secondary to an increase in intracellular sodium, by addition of veratrine (1μg/ml), or directly by either elevating [Ca2+]ofrom 2 to 5 mmor by exposing the cells to isoproterenol (1 to 100 nm). Veratrine exposure caused a time-dependent increase in both diastolic and systolic [Ca2+]ithat resulted in cellular calcium overload and hypercontraction. The rate of increase in [Ca2+]iwas more rapid in IAA-treated than in untreated myocytes, leading to a 13±3v5±2% increase (P<0.05) in diastolic [Ca2+]iafter 5 min of exposure. The corresponding increases in systolic [Ca2+]iwere 43±6 and 24±5% (P<0.05). Elevated [Ca2+]oresulted in increased [Ca2+]itransient amplitudes and cell shortening. These responses were each attenuated by inhibiting glycolysis, so that the increase was 38±5v68±9% ([Ca2+]itransient amplitude,P<0.05) and 41±11v91±18% (cell shortening,P<0.05). Inhibition of glycolysis did not, however, affect the increase in calcium transient or cell shortening during addition of isoproterenol. We conclude that glycolysis plays an essential role in the maintenance of intracellular calcium homeostasis during severe calcium overload. Glycolysis was also essential for signalling the inotropic effect that accompanied elevation in extracellular calcium, while the changes in intracellular calcium following administration of isoproterenol were not influenced by glycolysis in the present model.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>9769226</pmid><doi>10.1006/jmcc.1998.0732</doi><tpages>10</tpages></addata></record> |
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| subjects | Adenosine triphosphate metabolism Adrenergic beta-Agonists - pharmacology Animals Calcium - physiology Calcium Channels - drug effects Calcium Channels - metabolism Calcium homeostasis Calcium influx Fura-2 Glucose metabolism Glycolysis Glycolysis - physiology Heart - drug effects Heart - physiology Homeostasis - drug effects Inotropic stimuli Iodoacetate Iodoacetates - pharmacology Isoproterenol Isoproterenol - pharmacology Male Microscopy, Fluorescence Rat Rats Rats, Sprague-Dawley Ventricular cell Veratrine Veratrine - pharmacology |
| title | The Role of Glycolysis in Myocardial Calcium Control |
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