Influence of stereoisomers of 4-fluoroglutamate on rat brain glutamate decarboxylase.

J Drsata, M Netopilová, V Tolman
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引用次数: 3

Abstract

Inhibition of rat brain glutamate decarboxylase (GAD, EC 4.1.1.15) by individual stereoisomers of 4-fluoroglutamate (4-F-Glu) and 2-fluoro-4-aminobutyrate (2-F-GABA) was studied. All stereoisomers of 4-F-Glu inhibited decarboxylation of L-glutamate catalysed by the enzyme preparation. At 1 x 10(-2) M concentration, the most potent inhibitor of GAD was D-erythro-4-F-Glu with about 70% inhibition in the presence of 1.23 x 10(-2)M L-glutamate. The inhibition by all stereoisomers was of the competitive type. Ki values ranged from 2 x 10(-3)M for the D-erythro isomer to 1.1 x 10(-2)M for the D-threo and L-erythro isomers. The influence of all stereoisomers was reversible as shown by dialysis except for a small amount in the case of the D-erythro isomer. The inhibition was independent of external pyridoxal-5'-phosphate added. No inhibition of rat brain GAD was found with 2-fluoro-4-aminobutyrate stereoisomers.

4-氟谷氨酸立体异构体对大鼠脑谷氨酸脱羧酶的影响。
研究了4-氟谷氨酸酯(4-F-Glu)和2-氟-4-氨基丁酸酯(2-F-GABA)立体异构体对大鼠脑谷氨酸脱羧酶(GAD, EC 4.1.1.15)的抑制作用。4- f -谷氨酸的所有立体异构体均抑制酶制剂催化的l -谷氨酸脱羧。在1 × 10(-2)M浓度下,最有效的GAD抑制剂是d - red -4- f -glu,在1.23 × 10(-2)M l -谷氨酸存在时,其抑制率约为70%。所有立体异构体的抑制均为竞争性抑制。Ki值从d - thro异构体的2 × 10(-3)M到d - thro和l - thro异构体的1.1 × 10(-2)M不等。除少量的d -红细胞异构体外,所有立体异构体的影响都是可逆的。抑制作用不受外源吡哆醛-5′-磷酸的影响。2-氟-4-氨基丁酸酯立体异构体对大鼠脑GAD无抑制作用。
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