Hwang E C, Van Woert M H
Res Commun Chem Pathol Pharmacol. 1979 Mar;23(3):419-31.
p-methoxyphenlethylamine (p-MPEA) induces the "serotonin syndrome" in mice which consists of lateral head weaving, Straub tail, hindlimb abduction, tremor, hyperactivity, reciprocal fore-paw treading, salivation and piloerection. These p-MPEA-induced behavioral signs were partially prevented by pretreatment with serotonin (5HT) uptake blockers (fluoxetine, chlorimipramine, Org 6582) and 5HT receptor blockers (methiothepin, methysergide, cinnanserin) but not by two depletors of brain 5HT (p-chlorophenylalanine, reserpine). p-MPEA selectively released 5HT and inhibited 5HT uptake from mouse whole brain synaptosomes. The concentrations of both 5HT and 5-hydroxyindoleacetic acid (5HIAA) in whole mouse brain were increased at 1 and 2 hours after injection of p-MPEA (50 mg/kg). The effect of p-MPEA on displacement of specific tritiated 5HT binding to membranes from mouse brain was considerably less than that of p-chlorophenylethylamine (p-CPEA), p-methoxytryptamine (pMT) and quipazine. Thus p-MPEA may induce the "serotonin syndrome" predominantly by releasing 5HT from presynaptic nerve terminals.
对甲氧基苯乙胺(p-MPEA)可在小鼠中诱发“血清素综合征”,其表现为头部侧向摆动、施特劳布尾、后肢外展、震颤、多动、前爪交替踏地、流涎和竖毛。血清素(5HT)摄取阻滞剂(氟西汀、氯米帕明、Org 6582)和5HT受体阻滞剂(甲硫噻嗪、甲基麦角新碱、肉桂硫胺)预处理可部分预防这些由p-MPEA诱发的行为体征,但两种脑5HT耗竭剂(对氯苯丙氨酸、利血平)则不能。p-MPEA可选择性地释放5HT并抑制小鼠全脑突触体对5HT的摄取。注射p-MPEA(50毫克/千克)后1小时和2小时,小鼠全脑5HT和5-羟吲哚乙酸(5HIAA)的浓度均升高。p-MPEA对从小鼠脑细胞膜上置换特异性氚标记5HT结合的作用远小于对氯苯乙胺(p-CPEA)、对甲氧基色胺(pMT)和喹哌嗪。因此,p-MPEA可能主要通过从突触前神经末梢释放5HT来诱发“血清素综合征”。