Sogawa C, Sogawa N, Tagawa J, Fujino A, Ohyama K, Asanuma M, Funada M, Kitayama S
Department of Dental Pharmacology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Shikata 2-5-1, Okayama 700-8525, Japan.
Toxicol Lett. 2007 Apr 5;170(1):75-82. doi: 10.1016/j.toxlet.2007.02.007. Epub 2007 Feb 21.
5-Methoxy-N,N-diisopropyltryptamine (5-MeO-DIPT) is a synthetic orally active hallucinogenic tryptamine derivative, known also as Foxy or Foxy methoxy. However, few studies have examined its effects in vitro. In the present study, we investigated the actions of 5-MeO-DIPT against monoamine neurotransmitter transporters, including the transporters for dopamine (DAT), norepinephrine (NET), and serotonin (SERT), using COS-7 cells heterologously expressing these transporters and rat brain synaptosomes. 5-MeO-DIPT specifically inhibited the uptake of [3H]serotonin (5-HT) by the SERT-expressing COS-7 cells and rat striatal synaptosomes in a high affinity manner at concentrations similar to those for cocaine. The effect was reversible and competitive. 5-MeO-DIPT failed to stimulate reverse transport of [3H]5-HT through SERT, while it prevented the releasing action of methamphetamine. 5-MeO-DIPT induced cell toxicity at high concentrations in COS-7 cells, and it was not influenced by the expression of SERT. These results demonstrated that 5-MeO-DIPT acts as a competitive SERT inhibitor and has an inability to cause reverse transport, underlying its serotonergic actions.
5-甲氧基-N,N-二异丙基色胺(5-MeO-DIPT)是一种合成的口服活性致幻性色胺衍生物,也被称为“狐狸”或“狐狸甲氧基”。然而,很少有研究考察其体外效应。在本研究中,我们利用异源表达这些转运体的COS-7细胞和大鼠脑突触体,研究了5-MeO-DIPT对单胺神经递质转运体的作用,这些转运体包括多巴胺(DAT)、去甲肾上腺素(NET)和5-羟色胺(5-HT)转运体(SERT)。5-MeO-DIPT以与可卡因相似的浓度,以高亲和力的方式特异性抑制表达SERT的COS-7细胞和大鼠纹状体突触体对[3H]5-羟色胺(5-HT)的摄取。该效应是可逆且具有竞争性的。5-MeO-DIPT未能刺激[3H]5-HT通过SERT的反向转运,同时它阻止了甲基苯丙胺的释放作用。5-MeO-DIPT在高浓度时在COS-7细胞中诱导细胞毒性,且不受SERT表达的影响。这些结果表明,5-MeO-DIPT作为一种竞争性SERT抑制剂,无法引起反向转运,这是其5-羟色胺能作用的基础。