Ketamine-like effects of a combination of olanzapine and fluoxetine on AMPA and NMDA receptor-mediated transmission in the medial prefrontal cortex of the rat

被引:30
|
作者
Bjorkholm, Carl [1 ]
Jardemark, Kent [1 ]
Schilstrom, Bjorn [1 ]
Svensson, Torgny H. [1 ]
机构
[1] Karolinska Inst, Dept Physiol & Pharmacol, Sect Neuropsychopharmacol, SE-17177 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
Antidepressive agents; Antipsychotic agents; Major depressive disorder; Electrophysiology; Dopamine D1 receptors; Glutamate receptors; ELECTRICALLY-EVOKED RESPONSES; METHYL-D-ASPARTATE; PYRAMIDAL CELLS; DOPAMINE; NEURONS; DEPRESSION; CLOZAPINE; NEUROTRANSMISSION; AUGMENTATION; POTENTIATION;
D O I
10.1016/j.euroneuro.2015.07.002
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Preclinical studies indicate that the rapid antidepressant effect of ketamine is dependent on activation of AMPA receptors in the medial prefrontal cortex (mPFC) resulting in a prolonged enhancement of glutamatergic transmission in the mPFC. In similarity, addition of atypical antipsychotic drugs (APDs) to SSRIs has also been found to induce a rapid and potent antidepressant effect. Using intracellular recordings in layer V/VI pyramidal cells of the rat mPFC in vitro, we found that a combination of low, clinically relevant concentrations of the atypical APD olanzapine and the SSRI fluoxetine facilitated NMDA and AMPA-induced currents in pyramidal cells via activation of dopamine D1 receptors. A single ketamine injection (10 mg/kg, 24 h before the experiment) enhanced AMPA-and apparently to some extent also NMDA-induced currents. Our results propose that the rapid and potent antidepressant effects of both treatments may be related to a common mechanism of action, namely facilitation of glutamatergic, in particular AMPA receptor-mediated transmission, in the mPFC. (C) 2015 Elsevier B.V. and ECNP. All rights reserved.
引用
收藏
页码:1842 / 1847
页数:6
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