Inhibition of serum aspartate aminotransferase induced by isoniazid administration in mice.

Acta vitaminologica et enzymologica Pub Date : 1984-01-01
R H Yamada, Y Wakabayashi, A Iwashima
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Abstract

Intraperitoneal administration of isoniazid (IN), an antituberculous drug, to mice at a dose of 100 mg/kg body weight induced significant inhibition of serum aspartate aminotransferase (AAT) in several hours. The original activity was not restored readily by in vitro treatment of the sera with pyridoxal phosphate (PLP), in contrast to the rapid activation, by the same treatment, of apoAAT in the sera from control mice. Prolonged incubation with PLP prior to the assay was required to restore most of the lost activity. Serum AAT activity enhanced by experimental and the reversal of the inhibition similarly required prolonged incubation with PLP. The results suggest the possibility that human serum AAT activity measured for clinical diagnosis may be underestimated in cases of IN overdose even if the conditions for in vitro PLP treatment of samples are sufficient for conversion of the apoenzyme to the holoenzyme.

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异烟肼对小鼠血清天冬氨酸转氨酶的抑制作用。
抗结核药物异烟肼(IN)以100 mg/kg体重的剂量腹腔注射小鼠,可在数小时内显著抑制血清天冬氨酸转氨酶(AAT)。在体外用磷酸吡哆醛(pyridoxal phosphate, PLP)处理血清后,apoAAT的原始活性不容易恢复,而在同样的处理下,对照小鼠血清中的apoAAT迅速激活。在实验之前,需要用PLP长时间孵育以恢复大部分失去的活性。血清AAT活性的增强和抑制的逆转同样需要延长与PLP的孵育时间。结果表明,即使体外PLP处理样品的条件足以将脱酶转化为全酶,用于临床诊断的人类血清AAT活性也可能被低估。
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