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Volumn 1771, Issue 4, 2007, Pages 533-543

Studies on the extra-mitochondrial CoA-ester formation of valproic and Δ4-valproic acids

Author keywords

4 Valproic acid; Acyl CoA synthetase; Drug induced steatosis; Fatty acid activation; Steatosis mechanism; Valproic acid

Indexed keywords

2 PROPYL 4 PENTENOIC ACID; ACYL COENZYME A; DRUG METABOLITE; LONG CHAIN FATTY ACID COENZYME A LIGASE; MEDIUM CHAIN FATTY ACID; VALPROIC ACID;

EID: 34047225451     PISSN: 13881981     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbalip.2007.01.010     Document Type: Article
Times cited : (20)

References (39)
  • 1
    • 0842287450 scopus 로고    scopus 로고
    • Mitochondrial β-oxidation
    • Bartlett K., and Eaton S. Mitochondrial β-oxidation. Eur. J. Biochem. 271 (2004) 462-469
    • (2004) Eur. J. Biochem. , vol.271 , pp. 462-469
    • Bartlett, K.1    Eaton, S.2
  • 4
    • 0030885712 scopus 로고    scopus 로고
    • Fatty acid activation
    • Watkins P.A. Fatty acid activation. Prog. Lipid Res. 36 1 (1997) 55-83
    • (1997) Prog. Lipid Res. , vol.36 , Issue.1 , pp. 55-83
    • Watkins, P.A.1
  • 6
    • 0031663753 scopus 로고    scopus 로고
    • Role of hepatic fatty acid:coenzyme A ligases in the metabolism of xenobiotic carboxylic acids
    • Knights K.M. Role of hepatic fatty acid:coenzyme A ligases in the metabolism of xenobiotic carboxylic acids. Clin. Exp. Pharmacol. Physiol. 25 (1998) 776-782
    • (1998) Clin. Exp. Pharmacol. Physiol. , vol.25 , pp. 776-782
    • Knights, K.M.1
  • 8
    • 0034232476 scopus 로고    scopus 로고
    • Xenobiotic-CoA ligases: kinetic and molecular characterization
    • Knights K.M., and Drogemuller C.J. Xenobiotic-CoA ligases: kinetic and molecular characterization. Curr. Drug Metab. 1 (2000) 49-66
    • (2000) Curr. Drug Metab. , vol.1 , pp. 49-66
    • Knights, K.M.1    Drogemuller, C.J.2
  • 9
    • 0242384922 scopus 로고    scopus 로고
    • Characterization of the Acyl-CoA synthetase activity of purified murine fatty acid transport protein 1
    • Hall A.M., Smith A.J., and Bernlohr D.A. Characterization of the Acyl-CoA synthetase activity of purified murine fatty acid transport protein 1. J. Biol. Chem. 278 (2003) 43008-43013
    • (2003) J. Biol. Chem. , vol.278 , pp. 43008-43013
    • Hall, A.M.1    Smith, A.J.2    Bernlohr, D.A.3
  • 10
    • 20444484799 scopus 로고    scopus 로고
    • Comparative biochemical studies of the murine fatty acid transport proteins (FATP) expressed in yeast
    • Dirusso C.C., Li H., Darwis D., Watkins P.A., Berger J., and Black P.N. Comparative biochemical studies of the murine fatty acid transport proteins (FATP) expressed in yeast. J. Biol. Chem. (2005) 16829-16837
    • (2005) J. Biol. Chem. , pp. 16829-16837
    • Dirusso, C.C.1    Li, H.2    Darwis, D.3    Watkins, P.A.4    Berger, J.5    Black, P.N.6
  • 11
    • 15744364393 scopus 로고    scopus 로고
    • Enzymatic properties of purified murine fatty acid transport protein 4 and analysis of acyl-CoA synthetase activities in tissues from FATP4 null mice
    • Hall A.M., Wiczer B.M., Herrmann T., Stremmel W., and Bernlohr D.A. Enzymatic properties of purified murine fatty acid transport protein 4 and analysis of acyl-CoA synthetase activities in tissues from FATP4 null mice. J. Biol. Chem. 280 (2005) 11948-11954
    • (2005) J. Biol. Chem. , vol.280 , pp. 11948-11954
    • Hall, A.M.1    Wiczer, B.M.2    Herrmann, T.3    Stremmel, W.4    Bernlohr, D.A.5
  • 12
    • 2942711830 scopus 로고    scopus 로고
    • New concept of cellular fatty acid uptake: role of fatty acid transport proteins and of caveolae
    • Pohl J., Ring A., Ehehalt R., Herrmann T., and Stremmel W. New concept of cellular fatty acid uptake: role of fatty acid transport proteins and of caveolae. Proc. Nutr. Soc. 63 (2004) 259-262
    • (2004) Proc. Nutr. Soc. , vol.63 , pp. 259-262
    • Pohl, J.1    Ring, A.2    Ehehalt, R.3    Herrmann, T.4    Stremmel, W.5
  • 13
    • 2642529465 scopus 로고    scopus 로고
    • Biochemical demonstration of the involvement of fatty acyl-CoA synthetase in fatty acid translocation across the plasma membrane
    • Schmelter T., Trigatti B.L., Gerber G.E., and Mangroo D. Biochemical demonstration of the involvement of fatty acyl-CoA synthetase in fatty acid translocation across the plasma membrane. J. Biol. Chem. 279 (2004) 24163-24170
    • (2004) J. Biol. Chem. , vol.279 , pp. 24163-24170
    • Schmelter, T.1    Trigatti, B.L.2    Gerber, G.E.3    Mangroo, D.4
  • 14
    • 33747484925 scopus 로고    scopus 로고
    • The soluble acyl-acyl carrier protein synthetase of Vibrio harveyi B392 is a member of the medium chain acyl-CoA synthetase family
    • Jiang Y., Chan C.H., and Cronan J.E. The soluble acyl-acyl carrier protein synthetase of Vibrio harveyi B392 is a member of the medium chain acyl-CoA synthetase family. Biochemistry 45 (2006) 10008-10019
    • (2006) Biochemistry , vol.45 , pp. 10008-10019
    • Jiang, Y.1    Chan, C.H.2    Cronan, J.E.3
  • 15
    • 0034634680 scopus 로고    scopus 로고
    • Very long-chain acyl-CoA synthetases: human "bubblegum" represents a new family of proteins capable of activating very long-chain fatty acids
    • Steinberg S.J., Morgenthaler J., Heinzer A.K., Smith K.D., and Watkins P.A. Very long-chain acyl-CoA synthetases: human "bubblegum" represents a new family of proteins capable of activating very long-chain fatty acids. J. Biol. Chem. 275 (2000) 35162-35169
    • (2000) J. Biol. Chem. , vol.275 , pp. 35162-35169
    • Steinberg, S.J.1    Morgenthaler, J.2    Heinzer, A.K.3    Smith, K.D.4    Watkins, P.A.5
  • 16
    • 0035816532 scopus 로고    scopus 로고
    • Acyl-CoA synthetase isoform 1, 4 and 5 are present in different subcellular membranes in rat liver and can be inhibited independently
    • Lewin T.M., Kim J.H., Granger D.A., Vance J.E., and Coleman R.A. Acyl-CoA synthetase isoform 1, 4 and 5 are present in different subcellular membranes in rat liver and can be inhibited independently. J. Biol. Chem. 276 (2001) 24674-24679
    • (2001) J. Biol. Chem. , vol.276 , pp. 24674-24679
    • Lewin, T.M.1    Kim, J.H.2    Granger, D.A.3    Vance, J.E.4    Coleman, R.A.5
  • 17
    • 0032944064 scopus 로고    scopus 로고
    • Characterization of a renal medium chain acyl-CoA synthetase responsible for glycine conjugation in mouse kidney mitochondria
    • Kasuya F., Igarashi K., and Fukui M. Characterization of a renal medium chain acyl-CoA synthetase responsible for glycine conjugation in mouse kidney mitochondria. Chem.-Biol. Interact. 118 (1999) 233-246
    • (1999) Chem.-Biol. Interact. , vol.118 , pp. 233-246
    • Kasuya, F.1    Igarashi, K.2    Fukui, M.3
  • 18
    • 0029810456 scopus 로고    scopus 로고
    • Purification and characterization of a medium chain acyl-coenzyme A synthetase
    • Kasuya F., Igarashi K., Fukui M., and Nokihara K. Purification and characterization of a medium chain acyl-coenzyme A synthetase. Drug. Metab. Dispos. 24 (1996) 879-883
    • (1996) Drug. Metab. Dispos. , vol.24 , pp. 879-883
    • Kasuya, F.1    Igarashi, K.2    Fukui, M.3    Nokihara, K.4
  • 19
    • 33646596626 scopus 로고    scopus 로고
    • Purification, characterization, and mass spectrometric sequencing of a medium chain acyl-CoA synthetase from mouse liver mitochondria and comparisons with the homologues of rat and bovine
    • Kasuya F., Tatsuki T., Ohta M., Kawai Y., and Igarashi K. Purification, characterization, and mass spectrometric sequencing of a medium chain acyl-CoA synthetase from mouse liver mitochondria and comparisons with the homologues of rat and bovine. Protein Expr. Purif. 47 (2006) 405-414
    • (2006) Protein Expr. Purif. , vol.47 , pp. 405-414
    • Kasuya, F.1    Tatsuki, T.2    Ohta, M.3    Kawai, Y.4    Igarashi, K.5
  • 20
    • 0037247845 scopus 로고    scopus 로고
    • Isolation sequencing and expression of a cDNA for the HXM-A form of xenobiotic/medium-chain fatty acid:CoA ligase from human liver mitochondria
    • Vessey D.A., Lau E., Kelley M., and Warren R.S. Isolation sequencing and expression of a cDNA for the HXM-A form of xenobiotic/medium-chain fatty acid:CoA ligase from human liver mitochondria. J. Biochem. Mol. Toxicol. 17 (2003) 1-6
    • (2003) J. Biochem. Mol. Toxicol. , vol.17 , pp. 1-6
    • Vessey, D.A.1    Lau, E.2    Kelley, M.3    Warren, R.S.4
  • 21
    • 34047227772 scopus 로고    scopus 로고
    • M.F.B. Silva, The mechanisms and interactions of mitochondrial metabolism of valproic acid, PhD thesis, Faculdade de Farmácia, Universidade de Lisboa, 2002.
  • 23
    • 0020575199 scopus 로고
    • Influence of valproic acid on hepatic carbohydrate and lipid metabolism
    • Becker C.M., and Harris R.A. Influence of valproic acid on hepatic carbohydrate and lipid metabolism. Arch. Biochem. Biophys. 223 (1983) 381-392
    • (1983) Arch. Biochem. Biophys. , vol.223 , pp. 381-392
    • Becker, C.M.1    Harris, R.A.2
  • 24
    • 0021646542 scopus 로고
    • The hepatotoxicity of valproic acid and its metabolites in rats. I. Toxicologic, biochemical and histopathologic studies
    • Kesterson J.W., Granneman G.R., and Machinist J.M. The hepatotoxicity of valproic acid and its metabolites in rats. I. Toxicologic, biochemical and histopathologic studies. Hepatology 4 (1984) 1143-1152
    • (1984) Hepatology , vol.4 , pp. 1143-1152
    • Kesterson, J.W.1    Granneman, G.R.2    Machinist, J.M.3
  • 25
    • 0026655249 scopus 로고
    • In vitro effects of valproate and valproate metabolites on mitochondrial oxidations: relevance of CoA sequestration to the observed inhibitions
    • Ponchaut S., van Hoof F., and Veitch K. In vitro effects of valproate and valproate metabolites on mitochondrial oxidations: relevance of CoA sequestration to the observed inhibitions. Biochem. Pharmacol. 43 (1992) 2435-2442
    • (1992) Biochem. Pharmacol. , vol.43 , pp. 2435-2442
    • Ponchaut, S.1    van Hoof, F.2    Veitch, K.3
  • 26
    • 0028214470 scopus 로고
    • The relationship between mitochondrial activation and toxicity of some substituted carboxylic acids
    • Yao K.-W., Mao L.-F., Luo M.J., and Schulz H. The relationship between mitochondrial activation and toxicity of some substituted carboxylic acids. Chem.-Biol. Interact. 90 (1994) 225-234
    • (1994) Chem.-Biol. Interact. , vol.90 , pp. 225-234
    • Yao, K.-W.1    Mao, L.-F.2    Luo, M.J.3    Schulz, H.4
  • 27
    • 0023870362 scopus 로고
    • Hepatic hydrolysis of octanoyl-CoA and valproyl-CoA in control and valproate-treated animals
    • Moore K.H., Decker B.P., and Schreefel F.P. Hepatic hydrolysis of octanoyl-CoA and valproyl-CoA in control and valproate-treated animals. Int. J. Biochem. 20 (1988) 175-178
    • (1988) Int. J. Biochem. , vol.20 , pp. 175-178
    • Moore, K.H.1    Decker, B.P.2    Schreefel, F.P.3
  • 31
    • 0022005538 scopus 로고
    • Studies on the biotransformation in the perfused rat liver of 2-n-propyl-4-pentenoic acid, a metabolite of the antiepileptic drug valproic acid. Evidence for the formation of chemically reactive intermediates
    • Rettenmeyer A.W., Prickett K.S., Gordon W.P., Bjorge S.M., Chang S.-L., Levy R.H., and Baillie T.A. Studies on the biotransformation in the perfused rat liver of 2-n-propyl-4-pentenoic acid, a metabolite of the antiepileptic drug valproic acid. Evidence for the formation of chemically reactive intermediates. Drug Metab. Dispos. 13 (1985) 81-96
    • (1985) Drug Metab. Dispos. , vol.13 , pp. 81-96
    • Rettenmeyer, A.W.1    Prickett, K.S.2    Gordon, W.P.3    Bjorge, S.M.4    Chang, S.-L.5    Levy, R.H.6    Baillie, T.A.7
  • 33
    • 0014645531 scopus 로고
    • High yield preparation of isolated rat liver parenchymal cells: a biochemical and fine structure study
    • Berry M.N., and Friend D.S. High yield preparation of isolated rat liver parenchymal cells: a biochemical and fine structure study. J. Cell Biol. 43 (1969) 506-520
    • (1969) J. Cell Biol. , vol.43 , pp. 506-520
    • Berry, M.N.1    Friend, D.S.2
  • 34
    • 0037174943 scopus 로고    scopus 로고
    • Diffusion of tricarboxylic acid cycle enzymes in the mitochondrial matrix in vivo
    • Haggie P.M., and Verkman A.S. Diffusion of tricarboxylic acid cycle enzymes in the mitochondrial matrix in vivo. J. Biol. Chem. 277 (2002) 40782-40788
    • (2002) J. Biol. Chem. , vol.277 , pp. 40782-40788
    • Haggie, P.M.1    Verkman, A.S.2
  • 37
    • 0029127584 scopus 로고
    • Inhibition of mitochondrial β-oxidation as a mechanism of hepatotoxicity
    • Fromenty B., and Pessayre D. Inhibition of mitochondrial β-oxidation as a mechanism of hepatotoxicity. Pharmacol. Ther. 67 (1995) 101-154
    • (1995) Pharmacol. Ther. , vol.67 , pp. 101-154
    • Fromenty, B.1    Pessayre, D.2


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