Grosso A, de Sousa R C
J Membr Biol. 1978;40 Spec No:305-21. doi: 10.1007/BF02026013.
Amphibian epithelia have been used as models for studying the effects of psychotropic drugs on membrane transport. Several of these agents added to the internal or to the external media, at concentrations greater than 10(-3) M, had inhibitory, "ouabain-like" effects on Na transport. In contrast, stimulatory, "vasopressin-like" effects were seen at lower concentrations. The stimulation was additive to that of oxytocin if the drug was present in the external solution but nonadditive if in the internal solution. On water transport, harmala alkaloids had a vasopressinomimetic action in toad skin, while inhibition was seen with Li and amitriptyline. To account for these multiple effects, it is hypothesized that psychotropic drugs act on the following cell targets: the Na pump, the cyclic nucleotide system, microtubules, and membrane calcium sites at the outer barrier of the epithelium. Direct, biochemical evidence is needed to substantiate this hypothesis.
两栖动物上皮已被用作研究精神药物对膜转运影响的模型。其中几种药物添加到内部或外部介质中,浓度大于10(-3)M时,对钠转运具有抑制性的“哇巴因样”作用。相比之下,在较低浓度下可观察到刺激性的“血管加压素样”作用。如果药物存在于外部溶液中,这种刺激作用与催产素的刺激作用相加;但如果存在于内部溶液中,则不具有相加性。关于水转运,哈尔满生物碱在蟾蜍皮肤中具有拟血管加压素作用,而锂和阿米替林则表现出抑制作用。为了解释这些多种效应,有人提出精神药物作用于以下细胞靶点:钠泵、环核苷酸系统、微管以及上皮外屏障处的膜钙位点。需要直接的生化证据来证实这一假设。