Arai Y, Kim S K, Kinemuchi H, Tadano T, Oyama K, Satoh N, Kisara K
Department of Pharmacology, School of Medicine, Showa University, Tokyo, Japan.
Brain Res Bull. 1991 Jul;27(1):81-4. doi: 10.1016/0361-9230(91)90284-q.
Intra- and extra-synaptosomal activity of monoamine oxidase-A (MAO-A) and -B (MAO-B), dopamine (DA) and its main metabolites were examined to clarify the mechanism of action(s) of p-hydroxyamphetamine (p-OHA) in animal behaviour mediated by central dopaminergic systems. Intrasynaptosomal DA was oxidized by MAO-A and MAO-B and this oxidation is inhibited by p-OHA. The inhibition is due to two effects: 1) uptake of DA is inhibited by p-OHA, and 2) p-OHA also inhibits intrasynaptosomal oxidation of DA by MAO-A and MAO-B. The inhibition of oxidation by MAO-A is predominant. Administration (ICV) of 80 and 160 micrograms p-OHA to mice, doses that cause various behavioural, significantly reduced striatal DA and 3,4-dihydroxyphenylacetic acid (DOPAC) levels, but greatly increased 3-methoxytyramine, without significantly changing homovanillic acid (HVA). The release of DA and blockade of DA uptake into dopaminergic neurons by p-OHA, together with preferential inhibition of the DA metabolizing enzyme, MAO-A, may contribute to p-OHA-induced behaviour mediated by the central dopaminergic systems.
为阐明对羟基苯丙胺(p - OHA)在由中枢多巴胺能系统介导的动物行为中的作用机制,研究了单胺氧化酶 - A(MAO - A)和 - B(MAO - B)、多巴胺(DA)及其主要代谢产物在突触体内外的活性。突触体内的DA被MAO - A和MAO - B氧化,且这种氧化被p - OHA抑制。该抑制作用归因于两种效应:1)p - OHA抑制DA的摄取;2)p - OHA还抑制MAO - A和MAO - B对突触体内DA的氧化。MAO - A对氧化的抑制作用占主导。向小鼠脑室内注射80和160微克p - OHA(可引起各种行为的剂量),显著降低了纹状体DA和3,4 - 二羟基苯乙酸(DOPAC)水平,但大幅增加了3 - 甲氧基酪胺,而高香草酸(HVA)无显著变化。p - OHA导致DA释放并阻断其向多巴胺能神经元的摄取,同时优先抑制DA代谢酶MAO - A,这可能有助于p - OHA诱导的由中枢多巴胺能系统介导的行为。