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使用三种不同底物对酗酒和精神分裂症患者的血小板单胺氧化酶进行测量。

Measurement of platelet monoamine oxidase using three different substrates in patients with alcoholism and schizophrenia.

作者信息

Tsuji M

出版信息

Folia Psychiatr Neurol Jpn. 1985;39(4):521-30. doi: 10.1111/j.1440-1819.1985.tb00806.x.

Abstract

The platelet monoamine oxidase (MAO) activities in alcoholism and schizophrenia were investigated by means of simultaneous determination, using beta-phenyl-ethylamine, tryptamine and serotonin as substrates. No significant difference was found between the MAO levels in the alcoholic and schizophrenic groups, when tryptamine was used as a substrate, but both groups showed lower values than the controls. On the other hand, beta-phenylethylamine, a specific substrate for MAO B used as a substrate, showed no significant difference between the alcoholic and control groups in the activities. These two groups showed higher values in MAO activity than the schizophrenic group, whereas when MAO activity was estimated using serotonin, platelet enzyme was found to be inhibited significantly in alcoholism, and the level of activities in the schizophrenics was similar to that of the controls. Moreover, the beta-phenylethylamine inhibition curve obtained serotonin as the substrate in the pooled platelets of 50 normal human subjects, and the MAO activity could not be inhibited by higher concentrations than the Km value of serotonin. These findings suggested that there might be two interacting catabolic sites having different substrate affinities in blood platelet MAO. Thus, it could be speculated that serotonergic catabolic sites of MAO in the platelets are disturbed in the alcoholics, while beta-phenylethylaminergic catabolic sites of platelet MAO are inherently vulnerable in schizophrenia.

摘要

采用同时测定的方法,以β-苯乙胺、色胺和5-羟色胺为底物,对酒精中毒和精神分裂症患者血小板单胺氧化酶(MAO)活性进行了研究。以色胺为底物时,酒精中毒组和精神分裂症组的MAO水平无显著差异,但两组均低于对照组。另一方面,以MAO-B的特异性底物β-苯乙胺为底物时,酒精中毒组和对照组的活性无显著差异。这两组的MAO活性高于精神分裂症组,而以5-羟色胺测定MAO活性时,发现酒精中毒患者血小板酶受到显著抑制,精神分裂症患者的活性水平与对照组相似。此外,在50名正常受试者的混合血小板中,以5-羟色胺为底物得到的β-苯乙胺抑制曲线显示,高于5-羟色胺Km值的浓度无法抑制MAO活性。这些发现提示,血小板MAO可能存在两个具有不同底物亲和力的相互作用的分解代谢位点。因此,可以推测,酒精中毒患者血小板中MAO的5-羟色胺能分解代谢位点受到干扰,而精神分裂症患者血小板MAO的β-苯乙胺能分解代谢位点本身就很脆弱。

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