Nano-selenium and the SRC family kinases pathway: Redefining gene expression dynamics in major depressive disorder based on a randomized controlled trial.

IF 0.5 Q4 CLINICAL NEUROLOGY
Morvarid Noormohammadi, Farnaz Etesam, Ali Amini, Pegah Khosravian, Morteza Mohammadzadeh, Farzad Shidfar
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引用次数: 0

Abstract

Background: Major depressive disorder (MDD) is a prevalent psychiatric condition. Dysregulation of signaling pathways interacting with SRC family kinases has been implicated in the pathophysiology of MDD through inflammation. Nano-selenium, a nanoscale form of selenium with enhanced bioavailability, has the potential to modulate oxidative stress and inflammation, which are implicated in MDD. To the best of our knowledge, in this study, for the first time we aimed to examine whether nano-selenium supplementation would decrease c-SRC gene expression. Methods: This triple-blind, randomized, placebo-controlled clinical trial was conducted at Imam Khomeini Hospital Complex, Tehran, Iran. Using block randomization, fifty participants diagnosed with MDD per Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-V) criteria were randomly assigned to receive nano-selenium (55 µg/day, n = 25) or placebo (n = 25) for 12 weeks alongside sertraline (50 mg/day). c-SRC gene expression was assessed using real-time reverse transcription quantitative polymerase chain reaction (RT-qPCR) from peripheral blood samples collected at baseline and after 12 weeks. Results: Twenty-one participants in each group completed the study, with an 84% retention rate in both groups. No serious adverse events were reported. There was no significant difference between groups at baseline. Post-intervention, c-SRC gene expression levels decreased in both the nano-selenium and placebo groups [median change (Q1, Q3): -0.0031, (-0.0065, -0.0005) vs. -0.0021 (-0.0085, 0), respectively; P < 0.05]; however, no significant differences were observed between the two groups (P = 0.606). Conclusion: Nano-selenium supplementation did not significantly modulate c-SRC gene expression. Limitations included a short duration. Future studies should explore alternative molecular pathways, higher supplementation doses, and treatment-naïve populations to better understand nano-selenium's therapeutic potential in MDD.

Abstract Image

Abstract Image

纳米硒和SRC家族激酶途径:基于随机对照试验重新定义重度抑郁症的基因表达动态。
背景:重度抑郁障碍(MDD)是一种常见的精神疾病。与SRC家族激酶相互作用的信号通路失调通过炎症参与了MDD的病理生理。纳米硒是一种具有增强生物利用度的纳米级形式的硒,具有调节氧化应激和炎症的潜力,这与MDD有关。据我们所知,在本研究中,我们首次旨在研究纳米硒补充剂是否会降低c-SRC基因表达。方法:该三盲、随机、安慰剂对照临床试验在伊朗德黑兰伊玛目霍梅尼医院进行。采用块随机化,50名根据精神障碍诊断与统计手册第五版(DSM-V)标准诊断为重度抑郁症的参与者被随机分配接受纳米硒(55 μ g/天,n = 25)或安慰剂(n = 25),为期12周,同时服用舍曲林(50 mg/天)。采用实时逆转录定量聚合酶链反应(RT-qPCR)从基线和12周后收集的外周血样本中评估c-SRC基因表达。结果:每组21名参与者完成了研究,两组的保留率均为84%。无严重不良事件报告。两组在基线时无显著差异。干预后,纳米硒组和安慰剂组的c-SRC基因表达水平均下降[中位变化(Q1, Q3)分别为-0.0031,(-0.0065,-0.0005)和-0.0021 (-0.0085,0);P < 0.05];但两组间差异无统计学意义(P = 0.606)。结论:纳米硒对c-SRC基因表达无显著调节作用。限制包括持续时间短。未来的研究应该探索其他分子途径、更高的补充剂量和treatment-naïve人群,以更好地了解纳米硒在MDD中的治疗潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Current Journal of Neurology
Current Journal of Neurology CLINICAL NEUROLOGY-
CiteScore
0.80
自引率
14.30%
发文量
30
审稿时长
12 weeks
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