Raiteri M, Del Carmine R, Bertollini A, Levi G
Eur J Pharmacol. 1977 Jan 21;41(2):133-43. doi: 10.1016/0014-2999(77)90202-3.
The interaction of sympathomimetic amines with the transport of 3H-noradrenaline (3H-NE), 3H-dopamine (3H-DA) and 3H-5-hydroxytryptamine (3H-5-HT) were investigated in rat hypothalamic (3H-NE) and striatal (3H-DA) and 3 H-5-HT) synaptosomes. Modifications in the phenylethylamine structure led to changes in activity towards biogenic amine uptake and release: (a) the introduction of a beta-OH group led to compounds less active in inhibiting uptake and stimulating release of 3H-NE, 3H-DA and 3H-5-HT, with the exception of 3H-NE release which was stimulated more by unlabeled 1-NE than by DA; (b) the introduction of phenolic-OH groups always led to compounds which were stronger uptake inhibitors and releasers of the three biogenic amines; (c) the alpha-methylation increased the potency towards uptake inhibition and release stimulation, with the exception of 3H-NE release: in fact, the releasing activity of phenylethylamine was suppressed by alpha-methylation; (d) the introduction of a -Cl group in the para position selectively potentiated the effects on 3H-5-HT uptake and release and generally depressed those on catecholamine transport.
在大鼠下丘脑(用于研究3H-去甲肾上腺素,即3H-NE)、纹状体(用于研究3H-多巴胺,即3H-DA)和3H-5-羟色胺(3H-5-HT)的突触体中,研究了拟交感神经胺与3H-去甲肾上腺素、3H-多巴胺和3H-5-羟色胺转运的相互作用。苯乙胺结构的改变导致其对生物胺摄取和释放的活性发生变化:(a)引入β-OH基团导致化合物在抑制3H-NE、3H-DA和3H-5-HT摄取以及刺激其释放方面活性降低,但未标记的1-NE比DA更能刺激3H-NE的释放;(b)引入酚羟基总是导致化合物成为三种生物胺更强的摄取抑制剂和释放剂;(c)α-甲基化增加了对摄取抑制和释放刺激的效力,但3H-NE释放除外:实际上,苯乙胺的释放活性被α-甲基化所抑制;(d)在对位引入-Cl基团选择性地增强了对3H-5-HT摄取和释放的影响,并且总体上抑制了对儿茶酚胺转运的影响。