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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Effects of mitochondria and o-methoxybenzoylalanine on 3-hydroxyanthranilic acid dioxygenase activity and quinolinic acid synthesis.
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Effects of mitochondria and o-methoxybenzoylalanine on 3-hydroxyanthranilic acid dioxygenase activity and quinolinic acid synthesis.

机译:线粒体和邻甲氧基苯甲酰丙氨酸对3-羟基邻氨基苯甲酸双加氧酶活性和喹啉酸合成的影响。

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摘要

The use of o-methoxybenzoylalanine, a selective kynureninase inhibitor, has been proposed with the aim of reducing brain synthesis of quinolinic acid, an excitotoxic tryptophan metabolite. In liver homogenates, however, this compound caused unexpected accumulation of 3-hydroxyanthranilic acid, the product of kynureninase activity and the precursor of quinolinic acid. To explain this observation, we investigated the interaction(s) of o-methoxybenzoylalanine with 3-hydroxyanthranilic acid dioxygenase, the enzyme responsible for quinolinic acid formation. When the purified enzyme or partially purified cytosol preparations were used, o-methoxybenzoylalanine did not affect 3-hydroxyanthranilic acid dioxygenase activity. However, a significant reduction of this enzymatic activity did occur when o-methoxybenzoylalanine was tested in the presence of mitochondria. It is interesting that addition of purified mitochondria to 3-hydroxyanthranilic acid dioxygenase preparations reduced the enzymatic activity and the synthesis of quinolinic acid. In vivo, administration of o-methoxybenzoylalanine significantly reduced quinolinic acid synthesis and content in both blood and brain of mice. Our results suggest that mitochondrial protein(s) interact(s) with soluble 3-hydroxyanthranilic acid dioxygenase and cause(s) modifications in the enzyme resulting in a decrease in its activity. These modifications also allow the enzyme to interact with o-methoxybenzoylalanine, thus leading to a further reduction in quinolinic acid synthesis.
机译:有人提出使用选择性的犬尿氨酸酶抑制剂邻甲氧基苯甲酰丙氨酸来减少大脑中兴奋性色氨酸代谢物喹啉酸的合成。然而,在肝脏匀浆中,该化合物导致3-羟基邻氨基苯甲酸意外积累,这种3-羟基邻氨基苯甲酸是犬尿氨酸酶活性的产物,是喹啉酸的前体。为了解释这一发现,我们研究了邻甲氧基苯甲酰丙氨酸与3-羟基邻氨基苯甲酸双加氧酶(负责喹啉酸形成的酶)之间的相互作用。当使用纯化的酶或部分纯化的细胞溶胶制剂时,邻甲氧基苯甲酰丙氨酸不影响3-羟基邻氨基苯甲酸双加氧酶的活性。然而,当在线粒体存在下测试邻甲氧基苯甲酰丙氨酸时,确实发生了这种酶活性的显着降低。有趣的是,将纯化的线粒体添加到3-羟基邻氨基苯甲酸双加氧酶制剂中会降低酶促活性和喹啉酸的合成。在体内,邻甲氧基苯甲酰丙氨酸的施用显着降低了小鼠血液和脑中喹啉酸的合成和含量。我们的结果表明线粒体蛋白与可溶性3-羟基邻氨基苯甲酸双加氧酶相互作用并引起酶的修饰,导致其活性降低。这些修饰还允许酶与邻甲氧基苯甲酰丙氨酸相互作用,从而导致喹啉酸合成的进一步减少。

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