Melde K, Jackson S, Bartlett K, Sherratt H S, Ghisla S
University of Konstanz, Federal Republic of Germany.
Biochem J. 1991 Mar 1;274 ( Pt 2)(Pt 2):395-400. doi: 10.1042/bj2740395.
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 less than 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.
我们描述了亚甲基环丙基甘氨酸对禁食大鼠的影响。给予100mg该氨基酸/kg体重后6小时,观察到血糖浓度下降75%,乳酸和丙酮酸增加。与低血糖素的报道效应[威廉姆森和威尔逊(1965年)《生物化学杂志》94卷,19c - 21c]相反,给予亚甲基环丙基甘氨酸后酮体的血浆浓度下降,血浆中支链氨基酸的浓度增加了6倍。在亚甲基环丙基甘氨酸中毒大鼠的肝脏线粒体中,癸酰肉碱或棕榈酸的氧化几乎完全被抑制。乙酰乙酰辅酶A和3 - 氧代酰基辅酶A硫解酶的活性分别降至对照的25%和不到10%。由于二羧酸和支链氨基酸氧化产物的排泄,出现了明显的酸尿症。给予亚甲基环丙基甘氨酸后,检测到有毒代谢物亚甲基环丙基甲酰辅酶A在线粒体基质中积累。同样,我们通过实验证实亚甲基环丙基乙酰辅酶A在与亚甲基环丙基丙酮酸一起孵育的线粒体中积累。