Smith P A, Walker R J
Br J Pharmacol. 1974 May;51(1):21-7. doi: 10.1111/j.1476-5381.1974.tb09627.x.
1 The equipotent molar ratios of a range of tryptamine analogues, as compared with 5-hydroxytryptamine (5-HT), have been determined on the basis of their ability to hyperpolarize the membrane potential of the Retzius cell of the leech, Hirudo medicinalis.2 The substitution of methyl, fluoro, chloro, methoxy or acetyl groups onto the 5-HT molecule progressively reduced the potency.3 5-Methoxylation or terminal N-methylation of tryptamine considerably increased the potency of tryptamine but these compounds tended to depolarize cells rather than cause hyperpolarization. In some experiments they were ineffective on preparations pretreated with 5-HT.4 It is suggested that these compounds may act by a different mechanism from the 5-hydroxylated indoles, perhaps involving a different receptor.
一系列色胺类似物与5-羟色胺(5-HT)相比的等效摩尔比,已根据它们使水蛭(医用水蛭)Retzius细胞的膜电位超极化的能力来确定。
在5-HT分子上取代甲基、氟、氯、甲氧基或乙酰基会逐渐降低效力。
色胺的5-甲氧基化或末端N-甲基化显著提高了色胺的效力,但这些化合物倾向于使细胞去极化而不是引起超极化。在一些实验中,它们对用5-HT预处理的制剂无效。
有人提出,这些化合物可能通过与5-羟基化吲哚不同的机制起作用,也许涉及不同的受体。