Department of Psychiatry and Human Behavior and Center for Psychiatric Neuroscience, University of Mississippi Medical Center, School of Medicine, Jackson, MS 39216, USA.
Neurosci Lett. 2010 Jan 29;469(3):380-4. doi: 10.1016/j.neulet.2009.12.032. Epub 2009 Dec 18.
The serotonin 1A receptor (5-HT1A) and its associated transcriptional regulators, five prime repressor element under dual repression (Freud-1) and nuclear-deformed epidermal autoregulatory factor (NUDR/Deaf-1) have been previously found to be the repressors for 5-HT1A in the serotonergic raphe neurons, and are also altered in postmortem brains of individuals with major depressive disorder (MDD) and in rats exposed to chronic restraint stress. We sought to find out if rats exposed to chronic social defeat (CSD) stress also show altered expression of these genes. Adult male Wistar rats were exposed to CSD stress for four consecutive weeks following which they were sacrificed and gene expression assessed in the prefrontal cortex (PFC) by quantitative real-time polymerase chain reaction. While CSD had no significant effects on NUDR and Freud-1 mRNA levels, 5-HT1A mRNA levels were significantly downregulated in defeated animals. The data suggest that regulatory factors other than Freud-1 and NUDR may be involved in the regulation of 5-HT1A expression in PFC during CSD stress. Furthermore, decreased levels of 5-HT1A following social defeat in the PFC are consistent with human postmortem results for this receptor in major depression and demonstrate the possibility that this receptor is involved in the pathophysiology of depression and other stress related disorders.
5-羟色胺 1A 受体(5-HT1A)及其相关转录调节因子,双重抑制下的五端抑制元件(弗洛伊德-1)和核变形表皮自身调节因子(NUDR/Deaf-1)先前被发现是 5-羟色胺能中缝神经元中 5-HT1A 的抑制剂,并且在患有重度抑郁症(MDD)的个体的死后大脑中和在暴露于慢性束缚应激的大鼠中也发生改变。我们试图了解暴露于慢性社会挫败(CSD)应激的大鼠是否也表现出这些基因表达的改变。成年雄性 Wistar 大鼠连续四周暴露于 CSD 应激,然后处死并通过实时定量聚合酶链反应(PCR)评估前额叶皮质(PFC)中的基因表达。虽然 CSD 对 NUDR 和 Freud-1 mRNA 水平没有显著影响,但在被击败的动物中,5-HT1A mRNA 水平显著下调。数据表明,在 CSD 应激期间,除了 Freud-1 和 NUDR 之外,其他调节因子可能参与了 PFC 中 5-HT1A 表达的调节。此外,PFC 中社会挫败后 5-HT1A 水平的降低与该受体在重度抑郁症中的人类死后结果一致,表明该受体可能参与抑郁症和其他应激相关障碍的病理生理学。