Metabolic consequences of methylenecyclopropylglycine poisoning in rats
| dc.contributor.author | Melde, Klaus | deu |
| dc.contributor.author | Jackson, Sandra | deu |
| dc.contributor.author | Bartlett, Kim | deu |
| dc.contributor.author | Sherratt, H. Stanley A. | deu |
| dc.contributor.author | Ghisla, Sandro | |
| dc.date.accessioned | 2011-03-24T17:29:12Z | deu |
| dc.date.available | 2011-03-24T17:29:12Z | deu |
| dc.date.issued | 1991 | deu |
| dc.description.abstract | We describe the effects of methylenecyclopropylglycine in fasted rats. A 75% decrease in the blood glucose concentration and an increase of lactate and pyruvate were observed 6 h after administration of 100 mg of this amino acid/kg. By contrast with the effects reported for hypoglycin [Williamson & Wilson (1965) Biochem. J. 94, 19c-21c], the plasma concentrations of ketone bodies decreased after administration of methylenecyclopropylglycine and the concentrations of branched-chain amino acids in the plasma were increased 6-fold. The oxidation of decanoylcarnitine or of palmitate was nearly completely inhibited in rat liver mitochondria from methylenecyclopropylglycine-poisoned rats. The activities of acetoacetyl-CoA and of 3-oxoacyl-CoA thiolase were decreased to 25% and < 10% of the controls. There was a pronounced aciduria, due to the excretion of dicarboxylic acids and of oxidation products of branched-chain amino acids. The accumulation of the toxic metabolite methylenecyclopropylformyl-CoA in the mitochondrial matrix was detected after administration of methylenecyclopropylglycine. Similarly we confirmed experimentally that methylenecyclopropylacetyl-CoA accumulates in mitochondria incubated with methylenecyclopropylpyruvate. | eng |
| dc.description.version | published | |
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| dc.identifier.citation | First publ. in: Biochemical journal 274 (1991), pp. 395-400 | deu |
| dc.identifier.doi | 10.1042/bj2740395 | |
| dc.identifier.ppn | 279027826 | deu |
| dc.identifier.uri | http://kops.uni-konstanz.de/handle/123456789/6791 | |
| dc.language.iso | eng | deu |
| dc.legacy.dateIssued | 2008 | deu |
| dc.rights | Attribution-NonCommercial-NoDerivs 2.0 Generic | |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/2.0/ | |
| dc.subject.ddc | 570 | deu |
| dc.title | Metabolic consequences of methylenecyclopropylglycine poisoning in rats | eng |
| dc.type | JOURNAL_ARTICLE | deu |
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| kops.citation.bibtex | @article{Melde1991Metab-6791,
year={1991},
doi={10.1042/bj2740395},
title={Metabolic consequences of methylenecyclopropylglycine poisoning in rats},
number={2},
volume={274},
issn={0264-6021},
journal={Biochemical journal},
pages={395--400},
author={Melde, Klaus and Jackson, Sandra and Bartlett, Kim and Sherratt, H. Stanley A. and Ghisla, Sandro}
} | |
| kops.citation.iso690 | MELDE, Klaus, Sandra JACKSON, Kim BARTLETT, H. Stanley A. SHERRATT, Sandro GHISLA, 1991. Metabolic consequences of methylenecyclopropylglycine poisoning in rats. In: Biochemical journal. 1991, 274(2), pp. 395-400. ISSN 0264-6021. eISSN 1470-8728. Available under: doi: 10.1042/bj2740395 | deu |
| kops.citation.iso690 | MELDE, Klaus, Sandra JACKSON, Kim BARTLETT, H. Stanley A. SHERRATT, Sandro GHISLA, 1991. Metabolic consequences of methylenecyclopropylglycine poisoning in rats. In: Biochemical journal. 1991, 274(2), pp. 395-400. ISSN 0264-6021. eISSN 1470-8728. Available under: doi: 10.1042/bj2740395 | eng |
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<dcterms:abstract xml:lang="eng">We describe the effects of methylenecyclopropylglycine in fasted rats. A 75% decrease in the blood glucose concentration and an increase of lactate and pyruvate were observed 6 h after administration of 100 mg of this amino acid/kg. By contrast with the effects reported for hypoglycin [Williamson & Wilson (1965) Biochem. J. 94, 19c-21c], the plasma concentrations of ketone bodies decreased after administration of methylenecyclopropylglycine and the concentrations of branched-chain amino acids in the plasma were increased 6-fold. The oxidation of decanoylcarnitine or of palmitate was nearly completely inhibited in rat liver mitochondria from methylenecyclopropylglycine-poisoned rats. The activities of acetoacetyl-CoA and of 3-oxoacyl-CoA thiolase were decreased to 25% and < 10% of the controls. There was a pronounced aciduria, due to the excretion of dicarboxylic acids and of oxidation products of branched-chain amino acids. The accumulation of the toxic metabolite methylenecyclopropylformyl-CoA in the mitochondrial matrix was detected after administration of methylenecyclopropylglycine. Similarly we confirmed experimentally that methylenecyclopropylacetyl-CoA accumulates in mitochondria incubated with methylenecyclopropylpyruvate.</dcterms:abstract>
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