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Erschienen in: Journal of Inherited Metabolic Disease 3/2014

01.05.2014 | Original Article

Valproyl-CoA inhibits the activity of ATP- and GTP-dependent succinate:CoA ligases

verfasst von: Paula B. M. Luís, Jos Ruiter, Lodewijk IJlst, Isabel Tavares de Almeida, Marinus Duran, Ronald J. A. Wanders, Margarida F. B. Silva

Erschienen in: Journal of Inherited Metabolic Disease | Ausgabe 3/2014

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Abstract

Background

Valproic acid (VPA) is an effective antiepileptic drug that may induce progressive microvesicular steatosis. The impairment of mitochondrial function may be an important metabolic effect of VPA treatment with potential adverse consequences.

Objective

To investigate the influence of VPA on the activity of GTP- and ATP-specific succinate:CoA ligases (G-SUCL and A-SUCL).

Methods

The GTP- and ATP-specific SUCL activities were measured in human fibroblasts in the reverse direction, i.e. the formation of succinyl-CoA. These were assessed at different concentrations of succinate in the presence of VPA, valproyl-CoA and zinc chloride, an established inhibitor of the enzymes. Activities were measured using an optimized HPLC procedure.

Results

Valproyl-CoA (1 mM) inhibited the activity of A-SUCL and G-SUCL by 45-55 % and 25-50 %, respectively. VPA (1 mM) had no influence on the activity of the two enzymes.

Discussion

Valproyl-CoA appears to affect the activity of SUCL, especially with the ATP-specific enzyme. Considering the key role of SUCL in the Krebs cycle, interference with its activity might impair the cellular energy status. Moreover, A-SUCL is bound to the nucleoside diphosphate kinase (NDPK), which is responsible for the mitochondrial (deoxy)nucleotide synthesis. An inhibition of A-SUCL might influence the activity of NDPK inducing an imbalance of nucleotides in the mitochondria and eventually mitochondrial DNA depletion. This may account for the potential liver failure associated with valproate therapy, reported in patients with deficiencies within the mitochondrial DNA replicase system such as polymerase gamma 1.
Literatur
Zurück zum Zitat Aires CC, IJlst L, Stet F et al (2010a) Inhibition of hepatic carnitine palmitoyl-transferase I (CPT IA) by valproyl-CoA as a possible mechanism of valproate-induced steatosis. Biochem Pharmacol 79:792–799PubMedCrossRef Aires CC, IJlst L, Stet F et al (2010a) Inhibition of hepatic carnitine palmitoyl-transferase I (CPT IA) by valproyl-CoA as a possible mechanism of valproate-induced steatosis. Biochem Pharmacol 79:792–799PubMedCrossRef
Zurück zum Zitat Aires CC, van Cruchten A, IJlst L et al (2010b) New insights on the mechanisms of valproate-induced hyperammonemia: inhibition of hepatic N-acetylglutamate synthase activity by valproyl-CoA. J Hepatol 50:426–434 Aires CC, van Cruchten A, IJlst L et al (2010b) New insights on the mechanisms of valproate-induced hyperammonemia: inhibition of hepatic N-acetylglutamate synthase activity by valproyl-CoA. J Hepatol 50:426–434
Zurück zum Zitat Alberio S, Mineri R, Tiranti V, Zeviani M (2007) Depletion of mtDNA: syndromes and genes. Mitochondrion 7:6–12PubMedCrossRef Alberio S, Mineri R, Tiranti V, Zeviani M (2007) Depletion of mtDNA: syndromes and genes. Mitochondrion 7:6–12PubMedCrossRef
Zurück zum Zitat Bicknese AR, May W, Hickey WF, Dodson WE (1992) Early childhood hepatocerebral degeneration misdiagnosed as valproate hepatotoxicity. Ann Neurol 32:767–775PubMedCrossRef Bicknese AR, May W, Hickey WF, Dodson WE (1992) Early childhood hepatocerebral degeneration misdiagnosed as valproate hepatotoxicity. Ann Neurol 32:767–775PubMedCrossRef
Zurück zum Zitat Bogenhagen D, Clayton DA (1976) Thymidylate nucleotide supply for mitochondrial DNA synthesis in mouse L-cells. Effect of 5-fluorodeoxyuridine and methotrexate in thymidine kinase plus and thymidine kinase minus cells. J Biol Chem 251:2938–2944PubMed Bogenhagen D, Clayton DA (1976) Thymidylate nucleotide supply for mitochondrial DNA synthesis in mouse L-cells. Effect of 5-fluorodeoxyuridine and methotrexate in thymidine kinase plus and thymidine kinase minus cells. J Biol Chem 251:2938–2944PubMed
Zurück zum Zitat Bolanos JP, Medina JM (1993) Evidence of stimulation of the gamma-aminobutyric acid shunt by valproate and E-delta 2-valproate in neonatal rat brain. Mol Pharmacol 43:487–490PubMed Bolanos JP, Medina JM (1993) Evidence of stimulation of the gamma-aminobutyric acid shunt by valproate and E-delta 2-valproate in neonatal rat brain. Mol Pharmacol 43:487–490PubMed
Zurück zum Zitat Carrozzo R, Dionisi-Vici C, Steuerwald U et al (2007) SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness. Brain 130:862–874PubMedCrossRef Carrozzo R, Dionisi-Vici C, Steuerwald U et al (2007) SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness. Brain 130:862–874PubMedCrossRef
Zurück zum Zitat Cotariu D, Evans S, Zaidman JL (1985) Effect of sodium valproate on subcellular fraction enzymes in rat liver. Enzyme 34:196–200PubMed Cotariu D, Evans S, Zaidman JL (1985) Effect of sodium valproate on subcellular fraction enzymes in rat liver. Enzyme 34:196–200PubMed
Zurück zum Zitat El-Hattab AW, Scaglia F (2013) Mitochondrial DNA depletion syndromes: review and updates of genetic basis, manifestations, and therapeutic options. Neurotherapeutics 10:186–198PubMedCentralPubMedCrossRef El-Hattab AW, Scaglia F (2013) Mitochondrial DNA depletion syndromes: review and updates of genetic basis, manifestations, and therapeutic options. Neurotherapeutics 10:186–198PubMedCentralPubMedCrossRef
Zurück zum Zitat Elpeleg O, Miller C, Hershkovitz E et al (2005) Deficiency of the ADP-forming succinyl-CoA synthase activity is associated with encephalomyopathy and mitochondrial DNA depletion. Am J Hum Genet 76:1081–1086PubMedCentralPubMedCrossRef Elpeleg O, Miller C, Hershkovitz E et al (2005) Deficiency of the ADP-forming succinyl-CoA synthase activity is associated with encephalomyopathy and mitochondrial DNA depletion. Am J Hum Genet 76:1081–1086PubMedCentralPubMedCrossRef
Zurück zum Zitat Hakonen AH, Isohanni P, Paetau A, Herva R, Suomalainen A, Lonnqvist T (2007) Recessive Twinkle mutations in early onset encephalopathy with mtDNA depletion. Brain 130:3032–3040PubMedCrossRef Hakonen AH, Isohanni P, Paetau A, Herva R, Suomalainen A, Lonnqvist T (2007) Recessive Twinkle mutations in early onset encephalopathy with mtDNA depletion. Brain 130:3032–3040PubMedCrossRef
Zurück zum Zitat Johnson JD, Mehus JG, Tews K, Milavetz BI, Lambeth DO (1998) Genetic evidence for the expression of ATP- and GTP-specific succinyl-CoA synthetases in multicellular eucaryotes. J Biol Chem 273:27580–27586PubMedCrossRef Johnson JD, Mehus JG, Tews K, Milavetz BI, Lambeth DO (1998) Genetic evidence for the expression of ATP- and GTP-specific succinyl-CoA synthetases in multicellular eucaryotes. J Biol Chem 273:27580–27586PubMedCrossRef
Zurück zum Zitat Kadrmas EF, Ray PD, Lambeth DO (1991) Apparent ATP-linked succinate thiokinase activity and its relation to nucleoside diphosphate kinase in mitochondrial matrix preparations from rabbit. Biochim Biophys Acta 1074:339–346PubMedCrossRef Kadrmas EF, Ray PD, Lambeth DO (1991) Apparent ATP-linked succinate thiokinase activity and its relation to nucleoside diphosphate kinase in mitochondrial matrix preparations from rabbit. Biochim Biophys Acta 1074:339–346PubMedCrossRef
Zurück zum Zitat Kavanaugh-Black A, Connolly DM, Chugani SA, Chakrabarty AM (1994) Characterization of nucleoside-diphosphate kinase from Pseudomonas aeruginosa: complex formation with succinyl-CoA synthetase. Proc Natl Acad Sci U S A 91:5883–5887PubMedCentralPubMedCrossRef Kavanaugh-Black A, Connolly DM, Chugani SA, Chakrabarty AM (1994) Characterization of nucleoside-diphosphate kinase from Pseudomonas aeruginosa: complex formation with succinyl-CoA synthetase. Proc Natl Acad Sci U S A 91:5883–5887PubMedCentralPubMedCrossRef
Zurück zum Zitat Kowluru A, Tannous M, Chen HQ (2002) Localization and characterization of the mitochondrial isoform of the nucleoside diphosphate kinase in the pancreatic beta cell: evidence for its complexation with mitochondrial succinyl-CoA synthetase. Arch Biochem Biophys 398:160–169PubMedCrossRef Kowluru A, Tannous M, Chen HQ (2002) Localization and characterization of the mitochondrial isoform of the nucleoside diphosphate kinase in the pancreatic beta cell: evidence for its complexation with mitochondrial succinyl-CoA synthetase. Arch Biochem Biophys 398:160–169PubMedCrossRef
Zurück zum Zitat Lambeth DO, Tews KN, Adkins S, Frohlich D, Milavetz BI (2004) Expression of two succinyl-CoA synthetases with different nucleotide specificities in mammalian tissues. J Biol Chem 279:36621–36624PubMedCrossRef Lambeth DO, Tews KN, Adkins S, Frohlich D, Milavetz BI (2004) Expression of two succinyl-CoA synthetases with different nucleotide specificities in mammalian tissues. J Biol Chem 279:36621–36624PubMedCrossRef
Zurück zum Zitat Lamperti C, Fang M, Invernizzi F et al (2012) A novel homozygous mutation in SUCLA2 gene identified by exome sequencing. Mol Genet Metab 107:403–408PubMedCentralPubMedCrossRef Lamperti C, Fang M, Invernizzi F et al (2012) A novel homozygous mutation in SUCLA2 gene identified by exome sequencing. Mol Genet Metab 107:403–408PubMedCentralPubMedCrossRef
Zurück zum Zitat Leppik IE, Hovinga CA (2013) Extended-release antiepileptic drugs: a comparison of pharmacokinetic parameters relative to original immediate-release formulations. Epilepsia 54(1):28–35PubMedCrossRef Leppik IE, Hovinga CA (2013) Extended-release antiepileptic drugs: a comparison of pharmacokinetic parameters relative to original immediate-release formulations. Epilepsia 54(1):28–35PubMedCrossRef
Zurück zum Zitat Luis PB, Ruiter JP, Aires CC et al (2007) Valproic acid metabolites inhibit dihydrolipoyl dehydrogenase activity leading to impaired 2-oxoglutarate-driven oxidative phosphorylation. Biochim Biophys Acta 1767:1126–1133PubMedCrossRef Luis PB, Ruiter JP, Aires CC et al (2007) Valproic acid metabolites inhibit dihydrolipoyl dehydrogenase activity leading to impaired 2-oxoglutarate-driven oxidative phosphorylation. Biochim Biophys Acta 1767:1126–1133PubMedCrossRef
Zurück zum Zitat Luis PB, Ruiter JP, Ofman R et al (2011) Valproic acid utilizes the isoleucine breakdown pathway for its complete beta-oxidation. Biochem Pharmacol 82:1740–1746PubMedCrossRef Luis PB, Ruiter JP, Ofman R et al (2011) Valproic acid utilizes the isoleucine breakdown pathway for its complete beta-oxidation. Biochem Pharmacol 82:1740–1746PubMedCrossRef
Zurück zum Zitat Luis PB, Ruiter JP, IJlst L et al (2012) Inhibition of 3-methylcrotonyl-CoA carboxylase explains the increased excretion of 3-hydroxyisovaleric acid in valproate-treated patients. J Inherit Metab Dis 35:443–449PubMedCrossRef Luis PB, Ruiter JP, IJlst L et al (2012) Inhibition of 3-methylcrotonyl-CoA carboxylase explains the increased excretion of 3-hydroxyisovaleric acid in valproate-treated patients. J Inherit Metab Dis 35:443–449PubMedCrossRef
Zurück zum Zitat McFarland R, Hudson G, Taylor RW et al (2008) Reversible valproate hepatotoxicity due to mutations in mitochondrial DNA polymerase gamma (POLG1). Arch Dis Child 93:151–153PubMed McFarland R, Hudson G, Taylor RW et al (2008) Reversible valproate hepatotoxicity due to mutations in mitochondrial DNA polymerase gamma (POLG1). Arch Dis Child 93:151–153PubMed
Zurück zum Zitat Miller C, Wang L, Ostergaard E, Dan P, Saada A (2011) The interplay between SUCLA2, SUCLG2, and mitochondrial DNA depletion. Biochim Biophys Acta 1812:625–629PubMed Miller C, Wang L, Ostergaard E, Dan P, Saada A (2011) The interplay between SUCLA2, SUCLG2, and mitochondrial DNA depletion. Biochim Biophys Acta 1812:625–629PubMed
Zurück zum Zitat Navarro-Sastre A, Tort F, Garcia-Villoria J et al (2012) Mitochondrial DNA depletion syndrome: new descriptions and the use of citrate synthase as a helpful tool to better characterise the patients. Mol Genet Metab 107:409–415PubMed Navarro-Sastre A, Tort F, Garcia-Villoria J et al (2012) Mitochondrial DNA depletion syndrome: new descriptions and the use of citrate synthase as a helpful tool to better characterise the patients. Mol Genet Metab 107:409–415PubMed
Zurück zum Zitat Ostergaard E (2008) Disorders caused by deficiency of succinate-CoA ligase. J Inherit Metab Dis 31:226–229PubMed Ostergaard E (2008) Disorders caused by deficiency of succinate-CoA ligase. J Inherit Metab Dis 31:226–229PubMed
Zurück zum Zitat Ostergaard E, Hansen FJ, Sorensen N et al (2007) Mitochondrial encephalomyopathy with elevated methylmalonic acid is caused by SUCLA2 mutations. Brain 130:853–861PubMed Ostergaard E, Hansen FJ, Sorensen N et al (2007) Mitochondrial encephalomyopathy with elevated methylmalonic acid is caused by SUCLA2 mutations. Brain 130:853–861PubMed
Zurück zum Zitat Ostergaard E, Schwartz M, Batbayli M et al (2010) A novel missense mutation in SUCLG1 associated with mitochondrial DNA depletion, encephalomyopathic form, with methylmalonic aciduria. Eur J Pediatr 169:201–205PubMed Ostergaard E, Schwartz M, Batbayli M et al (2010) A novel missense mutation in SUCLG1 associated with mitochondrial DNA depletion, encephalomyopathic form, with methylmalonic aciduria. Eur J Pediatr 169:201–205PubMed
Zurück zum Zitat Peterson GM, Naunton M (2005) Valproate: a simple chemical with so much to offer. J Clin Pharm Ther 30:417–421PubMed Peterson GM, Naunton M (2005) Valproate: a simple chemical with so much to offer. J Clin Pharm Ther 30:417–421PubMed
Zurück zum Zitat Rouzier C, Le Guédard-Méreuze S, Fragaki K et al (2010) The severity of phenotype linked to SUCLG1 mutations could be correlated with residual amount of SUCLG1 protein. J Med Genet 47:670–676PubMed Rouzier C, Le Guédard-Méreuze S, Fragaki K et al (2010) The severity of phenotype linked to SUCLG1 mutations could be correlated with residual amount of SUCLG1 protein. J Med Genet 47:670–676PubMed
Zurück zum Zitat Saada A (2004) Deoxyribonucleotides and disorders of mitochondrial DNA integrity. DNA Cell Biol 23:797–806PubMed Saada A (2004) Deoxyribonucleotides and disorders of mitochondrial DNA integrity. DNA Cell Biol 23:797–806PubMed
Zurück zum Zitat Sakamoto O, Ohura T, Murayama K et al (2011) Neonatal lactic acidosis with methylmalonic aciduria due to novel mutations in the SUCLG1 gene. Pediatr Int 53:921–925PubMed Sakamoto O, Ohura T, Murayama K et al (2011) Neonatal lactic acidosis with methylmalonic aciduria due to novel mutations in the SUCLG1 gene. Pediatr Int 53:921–925PubMed
Zurück zum Zitat Saneto RP, Lee IC, Koenig MK et al (2010) POLG DNA testing as an emerging standard of care before instituting valproic acid therapy for pediatric seizure disorders. Seizure 19:140–146PubMedCentralPubMed Saneto RP, Lee IC, Koenig MK et al (2010) POLG DNA testing as an emerging standard of care before instituting valproic acid therapy for pediatric seizure disorders. Seizure 19:140–146PubMedCentralPubMed
Zurück zum Zitat Schmid MM, Freudenmann RW, Keller F et al (2013) Non-fatal and fatal liver failure associated with valproic acid. Pharmacopsychiatry 46:63–68PubMed Schmid MM, Freudenmann RW, Keller F et al (2013) Non-fatal and fatal liver failure associated with valproic acid. Pharmacopsychiatry 46:63–68PubMed
Zurück zum Zitat Silva MF, Ruiter JP, IJlst L et al (2001) Synthesis and intramitochondrial levels of valproyl-coenzyme A metabolites. Anal Biochem 290:60–67PubMed Silva MF, Ruiter JP, IJlst L et al (2001) Synthesis and intramitochondrial levels of valproyl-coenzyme A metabolites. Anal Biochem 290:60–67PubMed
Zurück zum Zitat Silva MF, Aires CC, Luis PB et al (2008) Valproic acid metabolism and its effects on mitochondrial fatty acid oxidation: a review. J Inherit Metab Dis 31:205–216PubMed Silva MF, Aires CC, Luis PB et al (2008) Valproic acid metabolism and its effects on mitochondrial fatty acid oxidation: a review. J Inherit Metab Dis 31:205–216PubMed
Zurück zum Zitat Stewart JD, Horvath R, Baruffini E et al (2010) Polymerase gamma gene POLG determines the risk of sodium valproate-induced liver toxicity. Hepatology 52:1791–1796PubMed Stewart JD, Horvath R, Baruffini E et al (2010) Polymerase gamma gene POLG determines the risk of sodium valproate-induced liver toxicity. Hepatology 52:1791–1796PubMed
Zurück zum Zitat Stumpf DA, McAfee J, Parks JK, Eguren L (1980) Propionate inhibition of succinate:CoA ligase (GDP) and the citric acid cycle in mitochondria. Pediatr Res 14:1127–1131PubMed Stumpf DA, McAfee J, Parks JK, Eguren L (1980) Propionate inhibition of succinate:CoA ligase (GDP) and the citric acid cycle in mitochondria. Pediatr Res 14:1127–1131PubMed
Zurück zum Zitat Turnbull DM, Bone AJ, Bartlett K, Koundakjian PP, Sherratt HS (1983) The effects of valproate on intermediary metabolism in isolated rat hepatocytes and intact rats. Biochem Pharmacol 32:1887–1892PubMed Turnbull DM, Bone AJ, Bartlett K, Koundakjian PP, Sherratt HS (1983) The effects of valproate on intermediary metabolism in isolated rat hepatocytes and intact rats. Biochem Pharmacol 32:1887–1892PubMed
Zurück zum Zitat Uusimaa J, Gowda V, McShane A et al (2013) Prospective study of POLG mutations presenting in children with intractable epilepsy-prevalence and clinical features. Epilepsia 54:1002–1011PubMedCentralPubMed Uusimaa J, Gowda V, McShane A et al (2013) Prospective study of POLG mutations presenting in children with intractable epilepsy-prevalence and clinical features. Epilepsia 54:1002–1011PubMedCentralPubMed
Zurück zum Zitat van Zoelen MA, de Graaf M, van Dijk MR et al (2012) Valproic acid-induced DRESS syndrome with acute liver failure. Neth J Med 70:155PubMed van Zoelen MA, de Graaf M, van Dijk MR et al (2012) Valproic acid-induced DRESS syndrome with acute liver failure. Neth J Med 70:155PubMed
Zurück zum Zitat Wider EA, Tigier HA (1971) Porphyrin biosynthesis in soybean callus tissue system. 8. Isolation, purification and general properties of succinyl CoA synthetase. Enzymologia 41:217–231PubMed Wider EA, Tigier HA (1971) Porphyrin biosynthesis in soybean callus tissue system. 8. Isolation, purification and general properties of succinyl CoA synthetase. Enzymologia 41:217–231PubMed
Metadaten
Titel
Valproyl-CoA inhibits the activity of ATP- and GTP-dependent succinate:CoA ligases
verfasst von
Paula B. M. Luís
Jos Ruiter
Lodewijk IJlst
Isabel Tavares de Almeida
Marinus Duran
Ronald J. A. Wanders
Margarida F. B. Silva
Publikationsdatum
01.05.2014
Verlag
Springer Netherlands
Erschienen in
Journal of Inherited Metabolic Disease / Ausgabe 3/2014
Print ISSN: 0141-8955
Elektronische ISSN: 1573-2665
DOI
https://doi.org/10.1007/s10545-013-9657-4

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