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Long-term consequences of chronic fluoxetine exposure on the expression of myelination-related genes in the rat hippocampus

机译:慢性氟西汀暴露对大鼠海马髓鞘相关基因表达的长期影响

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摘要

The selective serotonin reuptake inhibitor (SSRI) fluoxetine is widely prescribed for the treatment of symptoms related to a variety of psychiatric disorders. After chronic SSRI treatment, some symptoms remediate on the long term, but the underlying mechanisms are not yet well understood. Here we studied the long-term consequences (40 days after treatment) of chronic fluoxetine exposure on genome-wide gene expression. During the treatment period, we measured body weight; and 1 week after treatment, cessation behavior in an SSRI-sensitive anxiety test was assessed. Gene expression was assessed in hippocampal tissue of adult rats using transcriptome analysis and several differentially expressed genes were validated in independent samples. Gene ontology analysis showed that upregulated genes induced by chronic fluoxetine exposure were significantly enriched for genes involved in myelination. We also investigated the expression of myelination-related genes in adult rats exposed to fluoxetine at early life and found two myelination-related genes (Transferrin (Tf) and Ciliary neurotrophic factor (Cntf)) that were downregulated by chronic fluoxetine exposure. Cntf, a neurotrophic factor involved in myelination, showed regulation in opposite direction in the adult versus neonatally fluoxetine-exposed groups. Expression of myelination-related genes correlated negatively with anxiety-like behavior in both adult and neonatally fluoxetine-exposed rats. In conclusion, our data reveal that chronic fluoxetine exposure causes on the long-term changes in expression of genes involved in myelination, a process that shapes brain connectivity and contributes to symptoms of psychiatric disorders.
机译:选择性5-羟色胺再摄取抑制剂(SSRI)氟西汀被广泛处方用于治疗与各种精神疾病有关的症状。长期使用SSRI治疗后,可以长期缓解某些症状,但其潜在机制尚不清楚。在这里,我们研究了慢性氟西汀暴露对全基因组全基因表达的长期后果(治疗后40天)。在治疗期间,我们测量了体重。治疗后1周,评估SSRI敏感焦虑测试中的戒烟行为。使用转录组分析评估成年大鼠海马组织中的基因表达,并在独立样品中验证了几种差异表达的基因。基因本体分析表明,慢性氟西汀暴露诱导的上调基因显着丰富了涉及髓鞘形成的基因。我们还调查了早期与氟西汀接触的成年大鼠中与髓鞘相关的基因的表达,发现了两个与髓鞘相关的基因(转铁蛋白(Tf)和睫状神经营养因子(Cntf)),这些基因被慢性氟西汀的下调。 Cntf是一种参与髓鞘形成的神经营养因子,在成人和新生儿氟西汀暴露组中显示出相反的调节作用。在成人和新生儿氟西汀暴露的大鼠中,与髓鞘形成相关的基因的表达与焦虑样行为呈负相关。总之,我们的数据表明,长期氟西汀暴露会导致与髓鞘形成有关的基因表达的长期变化,这一过程会影响大脑的连通性并导致精神疾病的症状。

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