Effect of in vivo administration of ethylmalonic acid on energy metabolism in rat tissues
High concentrations of ethylmalonic acid (EMA) occur in tissues and biological fluids of patients affected by deficiency of short-chain acyl-CoA dehydrogenase activity, as well as in other illnesses characterized by neurological and muscular symptoms. Considering that the pathophysiological mechanis...
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creator | FERREIRA, Gustavo Da C ROTH ANDRE, Karina SCHUCK, Patricia Fernanda VIEGAS, Carolina M TONIN, Anelise DE MOURA COELHO, Daniella WYSE, Angela T. S WANNMACHER, Clovis M. D VARGAS, Carmen R WAJNER, Moacir |
description | High concentrations of ethylmalonic acid (EMA) occur in tissues and biological fluids of patients affected by deficiency of short-chain acyl-CoA dehydrogenase activity, as well as in other illnesses characterized by neurological and muscular symptoms. Considering that the pathophysiological mechanisms responsible for the clinical manifestations of these diseases are virtually unknown, in the present work we developed a chemical in vivo model of ethylmalonic acidemia in young Wistar rats for neurochemical and behavioral studies through subcutaneous administration of EMA to young rats. The doses of EMA administered subcutaneously varied according to the age of the animals, being injected 3, 4, and 6 micromol g(-1) of body weight in rats of 7, 14, and 21 days, respectively. The concentrations of the acid were measured in blood and brain at regular intervals after a single injection (30-120 min) and reached the highest concentrations (3.0 mM and 0.5 micromol g(-1), approximately 0.5 mM), respectively, after 30 and 60 min of EMA injection. Next, we investigated the effects of acute EMA administration on the activities of complexes I-III, II, II-III, and IV of the respiratory chain in cerebral cortex and skeletal muscle, as well as on the activity of creatine kinase in cerebral cortex, striatum, skeletal muscle, and cardiac muscle of rats of 14 days of life. Control rats were treated with saline in the same volumes. We verified EMA administration did not change these enzymatic activities in all tissues studied. Although transient high concentrations of EMA did not alter important parameters of energy metabolism, it cannot be ruled out that chronic administration of this organic acid would disrupt energy metabolism. |
doi_str_mv | 10.1007/s11011-006-9004-7 |
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S ; WANNMACHER, Clovis M. D ; VARGAS, Carmen R ; WAJNER, Moacir</creator><creatorcontrib>FERREIRA, Gustavo Da C ; ROTH ANDRE, Karina ; SCHUCK, Patricia Fernanda ; VIEGAS, Carolina M ; TONIN, Anelise ; DE MOURA COELHO, Daniella ; WYSE, Angela T. S ; WANNMACHER, Clovis M. D ; VARGAS, Carmen R ; WAJNER, Moacir</creatorcontrib><description>High concentrations of ethylmalonic acid (EMA) occur in tissues and biological fluids of patients affected by deficiency of short-chain acyl-CoA dehydrogenase activity, as well as in other illnesses characterized by neurological and muscular symptoms. Considering that the pathophysiological mechanisms responsible for the clinical manifestations of these diseases are virtually unknown, in the present work we developed a chemical in vivo model of ethylmalonic acidemia in young Wistar rats for neurochemical and behavioral studies through subcutaneous administration of EMA to young rats. The doses of EMA administered subcutaneously varied according to the age of the animals, being injected 3, 4, and 6 micromol g(-1) of body weight in rats of 7, 14, and 21 days, respectively. The concentrations of the acid were measured in blood and brain at regular intervals after a single injection (30-120 min) and reached the highest concentrations (3.0 mM and 0.5 micromol g(-1), approximately 0.5 mM), respectively, after 30 and 60 min of EMA injection. Next, we investigated the effects of acute EMA administration on the activities of complexes I-III, II, II-III, and IV of the respiratory chain in cerebral cortex and skeletal muscle, as well as on the activity of creatine kinase in cerebral cortex, striatum, skeletal muscle, and cardiac muscle of rats of 14 days of life. Control rats were treated with saline in the same volumes. We verified EMA administration did not change these enzymatic activities in all tissues studied. Although transient high concentrations of EMA did not alter important parameters of energy metabolism, it cannot be ruled out that chronic administration of this organic acid would disrupt energy metabolism.</description><identifier>ISSN: 0885-7490</identifier><identifier>EISSN: 1573-7365</identifier><identifier>DOI: 10.1007/s11011-006-9004-7</identifier><identifier>PMID: 16773468</identifier><identifier>CODEN: MBDIEE</identifier><language>eng</language><publisher>New York, NY: Springer</publisher><subject>Acidosis - metabolism ; Age Factors ; Animals ; Biological and medical sciences ; Blood. Blood coagulation. Reticuloendothelial system ; Butyryl-CoA Dehydrogenase - deficiency ; Cerebral Cortex - drug effects ; Cerebral Cortex - enzymology ; Electron Transport Complex I - metabolism ; Electron Transport Complex II - metabolism ; Electron Transport Complex III - metabolism ; Electron Transport Complex IV - metabolism ; Energy Metabolism - drug effects ; Energy Metabolism - physiology ; Enzyme Activation - drug effects ; Enzyme Activation - physiology ; Female ; Injections, Subcutaneous ; Male ; Malonates - blood ; Malonates - pharmacokinetics ; Medical sciences ; Muscle, Skeletal - drug effects ; Muscle, Skeletal - enzymology ; Myocardium - enzymology ; Neurology ; Neuropharmacology ; Neuroprotective agent ; Pharmacology. Drug treatments ; Pregnancy ; Rats ; Rats, Wistar</subject><ispartof>Metabolic brain disease, 2006-03, Vol.21 (1), p.29-39</ispartof><rights>2006 INIST-CNRS</rights><rights>Springer Science+Business Media, Inc. 2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c317t-6eb842c1feb400116f1316e475ae2abc23af30c4069a7d61cb054a7fd5675c603</citedby><cites>FETCH-LOGICAL-c317t-6eb842c1feb400116f1316e475ae2abc23af30c4069a7d61cb054a7fd5675c603</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18083919$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16773468$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>FERREIRA, Gustavo Da C</creatorcontrib><creatorcontrib>ROTH ANDRE, Karina</creatorcontrib><creatorcontrib>SCHUCK, Patricia Fernanda</creatorcontrib><creatorcontrib>VIEGAS, Carolina M</creatorcontrib><creatorcontrib>TONIN, Anelise</creatorcontrib><creatorcontrib>DE MOURA COELHO, Daniella</creatorcontrib><creatorcontrib>WYSE, Angela T. S</creatorcontrib><creatorcontrib>WANNMACHER, Clovis M. D</creatorcontrib><creatorcontrib>VARGAS, Carmen R</creatorcontrib><creatorcontrib>WAJNER, Moacir</creatorcontrib><title>Effect of in vivo administration of ethylmalonic acid on energy metabolism in rat tissues</title><title>Metabolic brain disease</title><addtitle>Metab Brain Dis</addtitle><description>High concentrations of ethylmalonic acid (EMA) occur in tissues and biological fluids of patients affected by deficiency of short-chain acyl-CoA dehydrogenase activity, as well as in other illnesses characterized by neurological and muscular symptoms. Considering that the pathophysiological mechanisms responsible for the clinical manifestations of these diseases are virtually unknown, in the present work we developed a chemical in vivo model of ethylmalonic acidemia in young Wistar rats for neurochemical and behavioral studies through subcutaneous administration of EMA to young rats. The doses of EMA administered subcutaneously varied according to the age of the animals, being injected 3, 4, and 6 micromol g(-1) of body weight in rats of 7, 14, and 21 days, respectively. The concentrations of the acid were measured in blood and brain at regular intervals after a single injection (30-120 min) and reached the highest concentrations (3.0 mM and 0.5 micromol g(-1), approximately 0.5 mM), respectively, after 30 and 60 min of EMA injection. Next, we investigated the effects of acute EMA administration on the activities of complexes I-III, II, II-III, and IV of the respiratory chain in cerebral cortex and skeletal muscle, as well as on the activity of creatine kinase in cerebral cortex, striatum, skeletal muscle, and cardiac muscle of rats of 14 days of life. Control rats were treated with saline in the same volumes. We verified EMA administration did not change these enzymatic activities in all tissues studied. Although transient high concentrations of EMA did not alter important parameters of energy metabolism, it cannot be ruled out that chronic administration of this organic acid would disrupt energy metabolism.</description><subject>Acidosis - metabolism</subject><subject>Age Factors</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blood. Blood coagulation. Reticuloendothelial system</subject><subject>Butyryl-CoA Dehydrogenase - deficiency</subject><subject>Cerebral Cortex - drug effects</subject><subject>Cerebral Cortex - enzymology</subject><subject>Electron Transport Complex I - metabolism</subject><subject>Electron Transport Complex II - metabolism</subject><subject>Electron Transport Complex III - metabolism</subject><subject>Electron Transport Complex IV - metabolism</subject><subject>Energy Metabolism - drug effects</subject><subject>Energy Metabolism - physiology</subject><subject>Enzyme Activation - drug effects</subject><subject>Enzyme Activation - physiology</subject><subject>Female</subject><subject>Injections, Subcutaneous</subject><subject>Male</subject><subject>Malonates - blood</subject><subject>Malonates - pharmacokinetics</subject><subject>Medical sciences</subject><subject>Muscle, Skeletal - drug effects</subject><subject>Muscle, Skeletal - enzymology</subject><subject>Myocardium - enzymology</subject><subject>Neurology</subject><subject>Neuropharmacology</subject><subject>Neuroprotective agent</subject><subject>Pharmacology. 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S</creator><creator>WANNMACHER, Clovis M. 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Reticuloendothelial system</topic><topic>Butyryl-CoA Dehydrogenase - deficiency</topic><topic>Cerebral Cortex - drug effects</topic><topic>Cerebral Cortex - enzymology</topic><topic>Electron Transport Complex I - metabolism</topic><topic>Electron Transport Complex II - metabolism</topic><topic>Electron Transport Complex III - metabolism</topic><topic>Electron Transport Complex IV - metabolism</topic><topic>Energy Metabolism - drug effects</topic><topic>Energy Metabolism - physiology</topic><topic>Enzyme Activation - drug effects</topic><topic>Enzyme Activation - physiology</topic><topic>Female</topic><topic>Injections, Subcutaneous</topic><topic>Male</topic><topic>Malonates - blood</topic><topic>Malonates - pharmacokinetics</topic><topic>Medical sciences</topic><topic>Muscle, Skeletal - drug effects</topic><topic>Muscle, Skeletal - enzymology</topic><topic>Myocardium - enzymology</topic><topic>Neurology</topic><topic>Neuropharmacology</topic><topic>Neuroprotective agent</topic><topic>Pharmacology. Drug treatments</topic><topic>Pregnancy</topic><topic>Rats</topic><topic>Rats, Wistar</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>FERREIRA, Gustavo Da C</creatorcontrib><creatorcontrib>ROTH ANDRE, Karina</creatorcontrib><creatorcontrib>SCHUCK, Patricia Fernanda</creatorcontrib><creatorcontrib>VIEGAS, Carolina M</creatorcontrib><creatorcontrib>TONIN, Anelise</creatorcontrib><creatorcontrib>DE MOURA COELHO, Daniella</creatorcontrib><creatorcontrib>WYSE, Angela T. S</creatorcontrib><creatorcontrib>WANNMACHER, Clovis M. 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S</au><au>WANNMACHER, Clovis M. D</au><au>VARGAS, Carmen R</au><au>WAJNER, Moacir</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of in vivo administration of ethylmalonic acid on energy metabolism in rat tissues</atitle><jtitle>Metabolic brain disease</jtitle><addtitle>Metab Brain Dis</addtitle><date>2006-03-01</date><risdate>2006</risdate><volume>21</volume><issue>1</issue><spage>29</spage><epage>39</epage><pages>29-39</pages><issn>0885-7490</issn><eissn>1573-7365</eissn><coden>MBDIEE</coden><abstract>High concentrations of ethylmalonic acid (EMA) occur in tissues and biological fluids of patients affected by deficiency of short-chain acyl-CoA dehydrogenase activity, as well as in other illnesses characterized by neurological and muscular symptoms. Considering that the pathophysiological mechanisms responsible for the clinical manifestations of these diseases are virtually unknown, in the present work we developed a chemical in vivo model of ethylmalonic acidemia in young Wistar rats for neurochemical and behavioral studies through subcutaneous administration of EMA to young rats. The doses of EMA administered subcutaneously varied according to the age of the animals, being injected 3, 4, and 6 micromol g(-1) of body weight in rats of 7, 14, and 21 days, respectively. The concentrations of the acid were measured in blood and brain at regular intervals after a single injection (30-120 min) and reached the highest concentrations (3.0 mM and 0.5 micromol g(-1), approximately 0.5 mM), respectively, after 30 and 60 min of EMA injection. Next, we investigated the effects of acute EMA administration on the activities of complexes I-III, II, II-III, and IV of the respiratory chain in cerebral cortex and skeletal muscle, as well as on the activity of creatine kinase in cerebral cortex, striatum, skeletal muscle, and cardiac muscle of rats of 14 days of life. Control rats were treated with saline in the same volumes. We verified EMA administration did not change these enzymatic activities in all tissues studied. Although transient high concentrations of EMA did not alter important parameters of energy metabolism, it cannot be ruled out that chronic administration of this organic acid would disrupt energy metabolism.</abstract><cop>New York, NY</cop><pub>Springer</pub><pmid>16773468</pmid><doi>10.1007/s11011-006-9004-7</doi><tpages>11</tpages></addata></record> |
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subjects | Acidosis - metabolism Age Factors Animals Biological and medical sciences Blood. Blood coagulation. Reticuloendothelial system Butyryl-CoA Dehydrogenase - deficiency Cerebral Cortex - drug effects Cerebral Cortex - enzymology Electron Transport Complex I - metabolism Electron Transport Complex II - metabolism Electron Transport Complex III - metabolism Electron Transport Complex IV - metabolism Energy Metabolism - drug effects Energy Metabolism - physiology Enzyme Activation - drug effects Enzyme Activation - physiology Female Injections, Subcutaneous Male Malonates - blood Malonates - pharmacokinetics Medical sciences Muscle, Skeletal - drug effects Muscle, Skeletal - enzymology Myocardium - enzymology Neurology Neuropharmacology Neuroprotective agent Pharmacology. Drug treatments Pregnancy Rats Rats, Wistar |
title | Effect of in vivo administration of ethylmalonic acid on energy metabolism in rat tissues |
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