首页> 外文OA文献 >Oxidation and enzyme-activated irreversible inhibition of rat liver monoamine oxidase-B by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP).
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Oxidation and enzyme-activated irreversible inhibition of rat liver monoamine oxidase-B by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP).

机译:1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)对大鼠肝脏单胺氧化酶-B的氧化和酶激活的不可逆抑制作用。

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摘要

The compound 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), which produces symptoms resembling Parkinson's disease in humans, acts both as a substrate and an enzyme-activated irreversible inhibitor of the B-form of monoamine oxidase from rat liver. Analysis of the inhibitory process showed the compound to be considerably more efficient as a substrate than as an irreversible inhibitor, with about 17000 mol of product being formed per mol of enzyme inactivated. The half-time of the inhibitory process was about 22 min. With the A-form of the enzyme, the compound had a lower Km value and a considerably lower maximum velocity than the corresponding values obtained with the B-form. Under the conditions used in the present work the inhibition of the A-form of the enzyme was largely reversible.
机译:化合物1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)会产生类似于人的帕金森氏病的症状,它既是底物,又是酶激活的B型B型不可逆抑制剂。大鼠肝脏中的单胺氧化酶。抑制过程的分析表明,该化合物作为底物比作为不可逆抑制剂要有效得多,每摩尔灭活的酶形成约17000摩尔产物。抑制过程的半衰期约为22分钟。对于酶的A-形式,该化合物具有比B-形式获得的相应值更低的Km值和明显更低的最大速度。在本发明所用的条件下,酶的A-形式的抑制在很大程度上是可逆的。

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