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Impact of antipsychotic medication on IL-6/STAT3 signaling axis in peripheral blood mononuclear cells of drug-naive schizophrenia patients

机译:抗精神病药对毒药 - 幼稚精神分裂症患者外周血单核细胞IL-6 / Stat3信号轴的影响

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Aim Immunopathogenesis remains a widely appreciated etiopathological model of schizophrenia. Persistent efforts have aimed to identify schizophrenia biomarkers indexing immune system abnormalities and also immuno-dampening effects of antipsychotic medications. Although data arising from published reports are encouraging, such studies are limited to a few immune parameters and not focused on a specific pathway. Th17 cells-mediated immuno-inflammatory responses have emerged as a potential mechanism in various neuropsychiatric conditions, including schizophrenia. The Th17 pathway is distinctly regulated through a coordinated action of multiple cytokines and transcription factors. In this study, we explored whether antipsychotic medication has any effect on the cytokines and transcription factors of the Th17 pathway. Methods A total of 27 drug-naive schizophrenia patients were recruited and followed up for 3 months after initiation of antipsychotic medication. Lymphocyte gene expression levels of two transcription factors (STAT3 and RORC) and one of their upstream regulators, IL6, were quantified before and after treatment. Plasma levels of cytokines, such as interleukin (IL)-1 beta, IL-6, IL-17A, IL-23, and IL-33, were also analyzed before and after treatment. Results Treatment with antipsychotic medication for 3 months resulted in significant downregulation of STAT3 gene expression as well as reduction in plasma levels of IL-1 beta, IL-6, and IL-17A. Significant reduction in total scores for the Scale for Assessment of Positive Symptoms and the Scale for Assessment of Negative Symptoms was also observed in schizophrenia patients after 3 months of antipsychotic treatment. Conclusion Our findings suggest possible immuno-modulatory effects of antipsychotic medication on the critical regulators, such as IL-6 and STAT3, of the Th17 pathway in schizophrenia patients. The IL-6/STAT3 signaling axis involved in the transcriptional regulation of Th17 cells might appear as an important target of antipsychotic treatment in schizophrenia patients. Alternatively, irrespective of the effect of antipsychotic drugs, the IL-6/STAT3 signaling axis might be crucially involved in ameliorating psychotic symptoms.
机译:AIM免疫病理学仍然是精神分裂症的广泛欣赏的精神分病学模型。持续努力旨在鉴定精神分裂症生物标志物指数免疫系统异常以及抗精神病药的免疫阻尼作用。虽然来自已发表的报告产生的数据令人鼓舞,但这些研究仅限于一些免疫参数,而不是专注于特定途径。 Th17细胞介导的免疫炎症反应在包括精神分裂症的各种神经精神病症中出现潜在机制。通过多种细胞因子和转录因子的协调作用清楚地调节TH17途径。在这项研究中,我们探讨了抗精神病药是否对Th17途径的细胞因子和转录因子有任何影响。方法在启动抗精神病药后,共招募了27例药物 - 幼稚精神分裂症患者3个月。淋巴细胞基因表达水平的两种转录因子(STAT3和RORC)和其上游调节剂IL6的一个在治疗之前和之后定量。在治疗之前和之后还分析了血浆细胞因子的细胞因子水平,例如白细胞介素(IL)-1β,IL-6,IL-17A,IL-33和IL-33。结果用抗精神病药治疗3个月,导致STAT3基因表达的显着下调,以及IL-1β,IL-6和IL-17A的血浆水平降低。在抗精神病药治疗3个月后,在精神分症患者中,还观察到阳性症状评估阳性症状规模的总分比显着降低,并观察到3个月的抗精神病药治疗。结论我们的研究结果表明,精神分裂症患者的临界调节剂对临界调节剂(如IL-6和Stat3)的可能免疫调节效果。涉及Th17细胞转录调节的IL-6 / Stat3信号轴可能显示为精神分裂症患者抗精神病患者的重要目标。或者,无论抗精神病药物的影响如何,IL-6 / Stat3信号轴可能是至关重要的精神病症状。

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