作者: ZoëA. Hughes , S.Clare Stanford
DOI: 10.1016/S0014-2999(96)00715-7
关键词: Desipramine 、 Neurotransmitter 、 Reuptake inhibitor 、 Fluoxetine 、 Chemistry 、 Mechanism of action 、 Pharmacology 、 Internal medicine 、 Citalopram 、 Serotonin reuptake inhibitor 、 Serotonin 、 Endocrinology
摘要: Abstract In microdialysis experiments in vivo, local infusion of either the selective serotonin reuptake inhibitor, fluoxetine, or noradrenaline uptake desipramine, increased efflux rat frontal cortex. Synaptosomal [3H]noradrenaline was used to test whether inhibition could contribute this effect fluoxetine. Low concentrations fluoxetine were less effective than desipramine at inhibiting uptake; both compounds more potent citalopram. To investigate involved an action on noradrenergic neurones, compared effects a lesion, induced by neurotoxin N-(2-chloroethyl)-N-ethyl-2-bromobenzylamine (DSP-4), and The lesion reduced presence citalopram but it desipramine. results suggest that actions non-noradrenergic mechanism is target for action.