Abstract | BACKGROUND: METHODS: Rat Acsl3-, Acsl6v1- and Acsl6v2-, and Acsl4-flag proteins were expressed in E. coli, and the ability of VPA to inhibit their activation of long-chain fatty acids to acyl-CoA was estimated using Michaelis-Menten kinetics. RESULTS: VPA uncompetitively inhibited Acsl4-mediated conversion of AA and of docosahexaenoic (DHA) but not of palmitic acid to acyl-CoA, but did not affect AA conversion by Acsl3, Acsl6v1 or Acsl6v2. Acsl4-mediated conversion of AA to AA- CoA showed substrate inhibition and had a 10-times higher catalytic efficiency than did conversion of DHA to DHA- CoA. Butyrate, octanoate, or lithium did not inhibit AA activation by Acsl4. CONCLUSIONS: VPA's ability to inhibit Acsl4 activation of AA and of DHA to their respective acyl-CoAs, when related to the higher catalytic efficiency of AA than DHA conversion, may account for VPA's selective reduction of AA turnover in rat brain phospholipids, and contribute to VPA's efficacy against bipolar disorder.
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Authors | Jakob A Shimshoni, Mireille Basselin, Lei O Li, Rosalind A Coleman, Stanley I Rapoport, Hiren R Modi |
Journal | Biochimica et biophysica acta
(Biochim Biophys Acta)
Vol. 1811
Issue 3
Pg. 163-9
(Mar 2011)
ISSN: 0006-3002 [Print] Netherlands |
PMID | 21184843
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, N.I.H., Intramural, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2010 Elsevier B.V. All rights reserved. |
Chemical References |
- Anticonvulsants
- Arachidonic Acids
- Isoenzymes
- Nerve Tissue Proteins
- Recombinant Proteins
- Docosahexaenoic Acids
- Arachidonic Acid
- Valproic Acid
- Acsl4 protein, rat
- Coenzyme A Ligases
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Topics |
- Acylation
(drug effects)
- Animals
- Anticonvulsants
(chemistry, pharmacology)
- Arachidonic Acid
(chemistry, metabolism)
- Arachidonic Acids
(chemistry, metabolism)
- Bipolar Disorder
(drug therapy, enzymology)
- Brain
(enzymology)
- Coenzyme A Ligases
(chemistry, genetics, metabolism)
- Docosahexaenoic Acids
(chemistry, metabolism)
- Enzyme Activation
(drug effects)
- Escherichia coli
- Humans
- Isoenzymes
(chemistry, metabolism)
- Nerve Tissue Proteins
(chemistry, metabolism)
- Rats
- Recombinant Proteins
(chemistry, metabolism)
- Valproic Acid
(chemistry, pharmacology)
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