Egashira T, Yamanaka Y
Department of Pharmacology, Oita Medical University, Japan.
Biochem Pharmacol. 1993 Aug 17;46(4):609-14. doi: 10.1016/0006-2952(93)90545-8.
The long-term effects of d-methamphetamine (MP, 5 mg/kg) on brain mitochondrial monoamine oxidase (MAO) activity were studied in mice given MP intraperitoneally daily for 4 weeks. The MAO activities decreased when serotonin (5-HT) and dopamine (DA) were used as substrates. A marked elevation in MAO activity was seen during MP withdrawal when 5-HT, DA, beta-phenylethylamine (beta-PEA) and norepinephrine (NE) were used as substrates. The kinetics of MAO showed a significant decrease in Km values, but no significant change in Vmax values during MP withdrawal, despite the presence of NE. The Km and Vmax values increased when NE was the substrate. Inhibition of MAO by MP or its metabolites (amphetamine, p-hydroxyamphetamine and p-hydroxymethamphetamine) increased with the use of the following substrates in the order: DA, 5-HT, NE and beta-PEA.
研究了 d-甲基苯丙胺(MP,5 毫克/千克)对小鼠脑线粒体单胺氧化酶(MAO)活性的长期影响,给小鼠每日腹腔注射 MP,持续 4 周。当以 5-羟色胺(5-HT)和多巴胺(DA)为底物时,MAO 活性降低。当以 5-HT、DA、β-苯乙胺(β-PEA)和去甲肾上腺素(NE)为底物时,在停用 MP 期间观察到 MAO 活性显著升高。MAO 的动力学显示,尽管存在 NE,但在停用 MP 期间 Km 值显著降低,而 Vmax 值无显著变化。当以 NE 为底物时,Km 和 Vmax 值增加。MP 或其代谢产物(苯丙胺、对羟基苯丙胺和对羟基甲基苯丙胺)对 MAO 的抑制作用,随着使用以下底物的顺序而增加:DA、5-HT、NE 和 β-PEA。