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Fluoxetine ameliorates depressive symptoms by regulating lncRNA expression in the mouse hippocampus

机译:氟西汀通过调节小鼠海马中的LNCRNA表达来改善抑郁症状

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摘要

Depression is a prevalent mental disorder that is associated with aging and contributes to increased mortality and morbidity. The overall prevalence of geriatric depression with clinically significant symptoms is currently on the rise. Recent studies have demonstrated that altered expressions of long non-coding RNAs (lncRNAs) in the brain affect neurodevelopment and manifest modulating functions during the depression. However, most lncRNAs have not yet been studied. Herein, we analyzed the transcriptome of dysregulated lncRNAs to reveal their expressions in a mouse model exhibiting depressive-like behaviors, as well as their corresponding response following antidepressant fluoxetine treatment. A chronic unpredictable mild stress (CUMS) mouse model was applied. A six-week fluoxetine intervention in CUMS-induced mice attenuated depressive-like behaviors. In addition, differential expression analysis of lncRNAs was performed following RNA-sequencing. A total of 282 lncRNAs (134 up-regulated and 148 down-regulated) were differentially expressed in CUMS-induced mice relative to non-stressed counterparts (P<0.05). Moreover, 370 differentially expressed lncRNAs were identified in CUMS-induced mice after fluoxetine intervention. Gene Ontology (GO) analyses showed an association between significantly dysregulated lncRNAs and protein binding, oxygen binding, and transport activity, while the Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis indicated that these dysregulated lncRNAs might be involved in inflammatory response pathways. Fluoxetine effectively ameliorated the symptoms of depression in CUMS-induced mice by regulating the expression of lncRNAs in the hippocampus. The findings herein provide valuable insights into the potential mechanism underlying depression in elderly people.
机译:抑郁症是一种普遍存在的精神障碍,与老化有关,有助于增加死亡率和发病率。目前临床显着症状的老年抑郁症的总体流行率目前正在上升。最近的研究表明,在抑制期间,脑中长期非编码RNA(LNCRNA)的长期非编码RNA(LNCRNA)的表达发生了改变的表达。然而,大多数LNCRNA尚未研究过。在此,我们分析了失去的LNCRNA的转录组,以揭示其在表现抑郁样行为的小鼠模型中的表达,以及它们在抗抑郁氟芬太汀治疗后的相应反应。应用慢性不可预测的轻度压力(CUMS)小鼠模型。六周的氟西汀干预患者诱导的小鼠减弱抑郁的行为。此外,在RNA测序后进行LNCRNA的差异表达分析。相对于非应激对应物,总共282个LNCRNA(134个上调和148个下调)在CUMS诱导的小鼠中差异地表达(P <0.05)。此外,在氟西汀干预后,在CUMS诱导的小鼠中鉴定了370个差异表达的LNCRNA。基因本体(GO)分析显示出显着失调的LNCRNA和蛋白质结合,氧合含量和运输活性之间的关联,而基因和基因组(KEGG)分析表明这些呼吸困难的LNCRNA可能涉及炎症反应途径。氟西汀通过调节海马中LNCRNA的表达,有效地改善了CUMS诱导的小鼠中抑郁症的症状。这里的结果为老年人的抑郁症潜在机制提供了有价值的见解。

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