Maj Institute of Pharmacology, Polish Academy of Sciences, Department of Pharmacology, 12 Smętna Street, Kraków, Poland.
Maj Institute of Pharmacology, Polish Academy of Sciences, Department of Neurochemistry, 12 Smętna Street, Kraków, Poland.
Behav Brain Res. 2020 Sep 1;393:112769. doi: 10.1016/j.bbr.2020.112769. Epub 2020 Jun 11.
According to preclinical and clinical studies, the antidepressant-induced increase in the activity of atypical antipsychotics may efficiently improve the treatment of negative and some cognitive symptoms of schizophrenia. In the present study, we aimed to evaluate the effects of the antidepressants escitalopram and mirtazapine and the atypical antipsychotic drug aripiprazole, administered separately or in combination, on the MK-801-induced deficits in the recognition memory test and on the extracellular levels of monoamines and their metabolites in the rat frontal cortex. Based on the results of the behavioral tests, co-treatment with an ineffective dose of aripiprazole (0.1 mg/kg) and escitalopram (2.5 and 5 mg/kg) or mirtazapine (5 mg/kg) abolished the deficits evoked by MK-801 in the novel object recognition test, and those effects were blocked by the 5-HT receptor antagonist (WAY 100,635) or the dopamine D receptor antagonist (SCH 23,390). Moreover, co-treatment with aripiprazole (0.3 mg/kg) and escitalopram (5 mg/kg) significantly increased the levels of noradrenaline and serotonin, decreased the level of its metabolite, and did not alter level of dopamine, but decreased the levels of its metabolites. In addition, co-treatment with aripiprazole (0.3 mg/kg) and mirtazapine (10 mg/kg) significantly increased the level of noradrenaline, did not change the levels of dopamine and serotonin, but increased the levels of their metabolites. Based on these results, the increase in the extracellular levels of noradrenaline or serotonin in the cortex induced by co-treatment with an antidepressant and aripiprazole may be very important for the pharmacotherapy of negative and some cognitive symptoms of schizophrenia.
根据临床前和临床研究,抗抑郁药诱导的非典型抗精神病药活性增加可能有效地改善精神分裂症的阴性和一些认知症状的治疗。在本研究中,我们旨在评估抗抑郁药艾司西酞普兰和米氮平以及非典型抗精神病药阿立哌唑分别或联合给药对 MK-801 诱导的识别记忆测试缺陷以及大鼠前额皮质中单胺及其代谢物的细胞外水平的影响。基于行为测试的结果,用无效剂量的阿立哌唑(0.1mg/kg)与艾司西酞普兰(2.5 和 5mg/kg)或米氮平(5mg/kg)联合治疗消除了 MK-801 引起的新型物体识别测试缺陷,而这些作用被 5-HT 受体拮抗剂(WAY 100,635)或多巴胺 D 受体拮抗剂(SCH 23,390)阻断。此外,阿立哌唑(0.3mg/kg)与艾司西酞普兰(5mg/kg)联合治疗显著增加去甲肾上腺素和 5-羟色胺的水平,降低其代谢物的水平,不改变多巴胺的水平,但降低其代谢物的水平。此外,阿立哌唑(0.3mg/kg)与米氮平(10mg/kg)联合治疗显著增加去甲肾上腺素的水平,不改变多巴胺和 5-羟色胺的水平,但增加其代谢物的水平。基于这些结果,抗抑郁药和阿立哌唑联合治疗诱导的皮质中去甲肾上腺素或 5-羟色胺的细胞外水平增加可能对精神分裂症的阴性和一些认知症状的药物治疗非常重要。