Berge O G, Chacho D, Hole K
Eur J Pharmacol. 1983 Jun 3;90(2-3):293-6. doi: 10.1016/0014-2999(83)90253-4.
5-Methoxy-N,N-dimethyltryptamine (5-MeODMT) in concentrations of 0.5-500 microM produced a significant inhibition of [14C]5-hydroxytryptamine [14C]5-HT) uptake in striatal, hippocampal and hypothalamic crude synaptosomes from rat brain. Higher concentrations of 5-MeODMT (10 microM) also inhibited the uptake of [3H]dopamine [3H]DA) and induced the release of [14C]5-HT and [3H]DA from preloaded synaptosomes. It appears that the 5-HT agonist properties of 5-MeODMT may involve reuptake inhibition in addition to the previously documented direct receptor stimulation.
浓度为0.5 - 500微摩尔的5-甲氧基-N,N-二甲基色胺(5-MeODMT)对大鼠脑纹状体、海马体和下丘脑粗制突触体中[14C]5-羟色胺([14C]5-HT)的摄取产生了显著抑制作用。更高浓度的5-MeODMT(10微摩尔)还抑制了[3H]多巴胺([3H]DA)的摄取,并诱导了预先加载的突触体中[14C]5-HT和[3H]DA的释放。看来,5-MeODMT的5-羟色胺激动剂特性除了先前记录的直接受体刺激外,可能还涉及再摄取抑制。