Literature DB >> 6766992

Dipropylacetate and aminoaciduria.

S Similä, L von Wendt, S L Linna.   

Abstract

Dipropylacetate (DPA) is an anticonvulsant, which has been successfully used in the treatment of several types of epilepsy. The mode of action has not yet been definitely elucidated, although evidence of influence on gamma aminobutyric acid (GABA) turnover in brain has been presented. Several recent reports of the occurrence of hyperglycinemia in association with DPA-treatment indicate that this agent also influences other areas of amino acid metabolism. In the present study of 10 patients receiving DPA for epilepsy, high concentrations of glycine in plasma and CSF were observed, whereas the levels of all other amino acids remained virtually unchanged. The effect of DPA on urinary excretion of amino acids seems to be of considerable significance as marked elevation of urine concentrations of alanine, asparagine, cystine, glycine, histidine, isoleucine and leucine, phenylalanine and tyrosine were observed. This secondary hyperglycinemia could be due to suppression of glycine conjugation reactions, whereas DPA or its metabolites might interfere with tubular reabsorption of various amino acids, thereby causing hyperaminoaciduria.

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Year:  1980        PMID: 6766992     DOI: 10.1016/s0022-510x(80)80009-8

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  6 in total

1.  Regional glycine receptor binding in the p,p'-DDT myoclonic rat model.

Authors:  M R Pranzatelli; K Tkach
Journal:  Arch Toxicol       Date:  1992       Impact factor: 5.153

2.  Valproate increases cerebrospinal fluid glutamine levels.

Authors:  J Jaeken; P Casaer; L Corbeel
Journal:  Eur J Pediatr       Date:  1987-01       Impact factor: 3.183

3.  Effect of chronic valproate treatment on folate-dependent methyl biosynthesis in the rat.

Authors:  G F Carl
Journal:  Neurochem Res       Date:  1986-05       Impact factor: 3.996

Review 4.  Valproate-associated hepatotoxicity and its biochemical mechanisms.

Authors:  M J Eadie; W D Hooper; R G Dickinson
Journal:  Med Toxicol Adverse Drug Exp       Date:  1988 Mar-Apr

5.  Plasma and cerebrospinal fluid amino acids in epileptic patients.

Authors:  Sirpa Rainesalo; Tapani Keränen; Johanna Palmio; Jukka Peltola; Simo S Oja; Pirjo Saransaari
Journal:  Neurochem Res       Date:  2004-01       Impact factor: 3.996

6.  Renal tubular dysfunction following treatment with anti-epileptic drugs.

Authors:  R Korinthenberg; L Wehrle; L B Zimmerhackl
Journal:  Eur J Pediatr       Date:  1994-11       Impact factor: 3.183

  6 in total

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