首页> 外文期刊>Progress in Neuro-Psychopharmacology & Biological Psychiatry: An International Research, Review and News Journal >Altered HDAC5 and CREB mRNA expressions in the peripheral leukocytes of major depression.
【24h】

Altered HDAC5 and CREB mRNA expressions in the peripheral leukocytes of major depression.

机译:抑郁症患者外周血白细胞中HDAC5和CREB ​​mRNA表达的改变。

获取原文
获取原文并翻译 | 示例
           

摘要

BACKGROUND: Gene expressions of the peripheral leukocytes in depressive patients might reflect the systemic dysfunction of major depression. We determined mRNA expression levels of Histone deacetylase 5 (HDAC5) gene and cyclic AMP response element-binding protein 1 (CREB) gene in the leukocyte of depressive patients. HDAC5 and CREB are reported to be important targets of antidepressants, the latter being located in the downstream of the former in lymphocyte calcium signaling. METHODS: 25 patients with major depression and 25 age- and sex-matched healthy controls were included in this study. Twenty patients were able to be followed up until the 8 week-treatment. The mRNA levels were determined by a quantitative RT-PCR method. RESULT: Levels of HDAC5 and CREB mRNA were significantly higher in drug-free depressive patients than those of controls and the higher mRNA levels decreased to control levels after 8-week paroxetine treatment. There were positive correlation between levels of HDAC5 and CREB. CONCLUSION: Our results suggest the alteration of HDAC5 and CREB gene expression in the systemic pathophysiology of major depression.
机译:背景:抑郁症患者外周血白细胞的基因表达可能反映了重度抑郁症的全身功能障碍。我们确定了抑郁症患者白细胞中组蛋白脱乙酰基酶5(HDAC5)基因和环状AMP响应元件结合蛋白1(CREB)基因的mRNA表达水平。据报道,HDAC5和CREB是抗抑郁药的重要靶标,后者在淋巴细胞钙信号传导中位于前者的下游。方法:本研究包括25例重度抑郁症患者和25例年龄和性别相匹配的健康对照者。直到8周治疗前,已有20位患者得到了随访。 mRNA水平通过定量RT-PCR方法确定。结果:帕罗西汀治疗8周后,无药抑郁症患者的HDAC5和CREB ​​mRNA水平显着高于对照组,而较高的mRNA水平则降至对照组。 HDAC5和CREB水平之间呈正相关。结论:我们的结果表明HDAC5和CREB基因表达的改变在重度抑郁症的全身病理生理中具有重要作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号