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Adjunctive treatment of brexpiprazole with fluoxetine shows a rapid antidepressant effect in social defeat stress model: Role of BDNF-TrkB signaling

机译:氟西汀辅助治疗brexpiprazole在社交挫败应激模型中显示快速抗抑郁作用:BDNF-TrkB信号传导的作用

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摘要

Addition of low doses of the atypical antipsychotic drug brexpiprazole with selective serotonin reuptake inhibitors (SSRIs) could promote antidepressant effect in patients with major depressive disorder although the precise mechanisms underlying the action of the combination are unknown. Combination of low dose of brexpiprazole (0.1 mg/kg) and SSRI fluoxetine (10 mg/kg) could promote a rapid antidepressant effect in social defeat stress model although brexpiprazole or fluoxetine alone did not show antidepressant effect. Furthermore, the combination significantly improved alterations in the brain-derived neurotrophic factor (BDNF) - TrkB signaling and dendritic spine density in the prefrontal cortex, hippocampus, and nucleus accumbens in the susceptible mice after social defeat stress. Interestingly, TrkB antagonist ANA-12 significantly blocked beneficial effects of combination of brexpiprazole and fluoxetine on depression-like phenotype. These results suggest that BDNF-TrkB signaling plays a role in the rapid antidepressant action of the combination of brexpiprazole and fluoxetine.
机译:低剂量的非典型抗精神病药brexpiprazole与选择性5-羟色胺再摄取抑制剂(SSRIs)的结合可增强重度抑郁症患者的抗抑郁作用,尽管该作用的确切机制尚不清楚。低剂量的brexpiprazole(0.1μg/ kg)和SSRI fluoxetine(10μmg/ kg)的组合可以在社交失败应激模型中促进快速的抗抑郁作用,尽管单独使用brexpiprazole或fluoxetine并没有抗抑郁作用。此外,该组合显着改善了社交挫败应激后易感小鼠脑源性神经营养因子(BDNF)-TrkB信号转导和伏隔前额叶皮质,海马和伏隔核中树突棘密度的变化。有趣的是,TrkB拮抗剂ANA-12显着阻断了brexpiprazole和fluoxetine联合使用对抑郁样表型的有益作用。这些结果表明,BDNF-TrkB信号转导在brexpiprazole和fluoxetine组合的快速抗抑郁作用中起作用。

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