Egashira T, Yamamoto T, Yamanaka Y
Department of Pharmacology, Medical College of Oita, Japan.
Jpn J Pharmacol. 1987 Sep;45(1):79-88. doi: 10.1254/jjp.45.79.
A and B form MAO activities in mitochondria and synaptosome were measured in the brain of monkeys administered d-methamphetamine (d-MP) 2 mg/kg, i.m., daily for 7 days. When mitochondria were used as an enzyme preparation, the Km and Vmax values decreased with 5-HT (serotonin for A-form MAO substrate) and beta-phenylethylamine (beta-PEA for B-form MAO substrate), while in the synaptosome, a significant increase of the Km and Vmax values was observed with 5-HT and dopamine as substrates. The mitochondrial MAO treated with d-MP was inhibited strongly by clorgyline and deprenyl with beta-PEA as a substrate, while synaptosomal MAO was highly sensitive to these MAO inhibitors with 5-HT as a substrate. MP and amphetamine (AP) were found in brain mitochondrial and synaptosomal preparations of monkeys administered 2 mg/kg d-MP, i.m. daily for 7 days; MP and AP contents were 5.05 +/- 0.22 pg/mg protein and 37.3 +/- 3.8 ng/mg protein in mitochondria and 2.35 +/- 0.35 pg/mg protein and 46.4 +/- 1.5 ng/mg protein in synaptosomes, respectively. MAO was inhibited by MP and its metabolites, AP p-hydroxymethamphetamine (OH-MP) and p-hydroxyamphetamine (OH-AP), with 5-HT, beta-PEA and dopamine as substrates, in vitro. MP and its metabolites were more potent inhibitors of A-form MAO than B-form MAO.
对每天肌肉注射2毫克/千克d-甲基苯丙胺(d-MP),持续7天的猴子大脑进行检测,测量线粒体和突触体中A和B形式的单胺氧化酶(MAO)活性。当将线粒体用作酶制剂时,以5-羟色胺(A形式MAO底物的血清素)和β-苯乙胺(B形式MAO底物的β-PEA)为底物时,米氏常数(Km)和最大反应速度(Vmax)值降低,而在突触体中,以5-羟色胺和多巴胺为底物时,观察到Km和Vmax值显著增加。以β-PEA为底物时,用d-MP处理的线粒体MAO受到氯吉兰和司来吉兰的强烈抑制,而突触体MAO以5-羟色胺为底物时对这些MAO抑制剂高度敏感。在每天肌肉注射2毫克/千克d-MP,持续7天的猴子大脑线粒体和突触体制剂中发现了MP和苯丙胺(AP);线粒体中MP和AP含量分别为5.05±0.22皮克/毫克蛋白和37.3±3.8纳克/毫克蛋白,突触体中分别为2.35±0.35皮克/毫克蛋白和46.4±1.5纳克/毫克蛋白。在体外,以5-羟色胺、β-PEA和多巴胺为底物时,MAO受到MP及其代谢产物AP对羟基甲基苯丙胺(OH-MP)和对羟基苯丙胺(OH-AP)的抑制。MP及其代谢产物对A形式MAO的抑制作用比对B形式MAO更强。