期刊文献+

TNF-α在抑郁症中的作用和机制研究 被引量:9

Tumor necrosis factor-α and its role in depression
原文传递
导出
摘要 抑郁症是一种情感精神疾病,临床上以显著而持久的心境低落为主要特征。抑郁症严重危害人们身心健康,降低生活质量,增加社会负担。抑郁的产生原因比较复杂,发病机制存在多种假说。在过去的几十年,虽然对于抑郁症的研究取得了一定的进展,但其确切的病因及病理生理机制目前仍不明确。近期,研究显示,促炎性细胞因子,尤其是肿瘤坏死因子-α(tumor necrosis factor-α,TNF-α)在抑郁症的发生、发展及临床药理机制中扮演着重要角色。现通过对TNF-α的生物学特征、在抑郁症发病和抗抑郁治疗中的作用、基因多态性与抑郁症关联性以及未来的应用与展望等进行综述,以期从多方面阐明TNF-α在抑郁症中的作用。 Depression is a mental disorder characterized by a pervasive and persistent low mood in clinic, which is associated with disability and reduced quality of life, as well as a significant social burden. Due to the multifactorial etiology factors of depression, there is a variety of pathogenesis hypothesis. Up to now, however, the pathogensis of depression still remains poorly understood. Most recently, there is a great deal of evidence that the pro-inflammatory cytokines, specifically, tumor necrosis factor-α (TNF-α) play a critical role in the development of depressive disorders and the mechanism of antidepressant treatment. In this paper, we focus on recent progress of the relationship between TNF-α and depressive disorders, and illustrate its biological characteristics, role in the pathophysiology, genetic susceptibility and future applications.
出处 《生命科学》 CSCD 2015年第5期574-581,共8页 Chinese Bulletin of Life Sciences
基金 国家自然科学基金项目(81260248) 云南省科技计划重点资助项目(2013FZ175) 青岛市科技局科技支撑计划(10-3-3-3-13-nsh)
关键词 抑郁症 肿瘤坏死因子-Α 病理生理 多态性 depression tumor necrosis factor-α pathophysiology polymorphism
  • 相关文献

参考文献88

  • 1Zunszain PA, I-Iepgul N, Pariante CM. Inflammation and depression. Curt Top Behav Neurosci, 2013, 14:135-51.
  • 2Murrough JW, Iacoviello B, Neumeister A, et al. Cogni- tive dysfunction in depression: neurocircuitry and new therapeutic strategies. Neurobiol Learn Mere, 2011, 96(4): 553-63.
  • 3Hashmi AM, Butt Z, Umair M. Is depression an inflamma- tory condition? A review of available evidence. J Pak Med Assoc, 2013, 63(7): 899-906.
  • 4Insel TR, Charney DS. Research on major depression: strategies and priorities. JAMA, 2003, 289(23): 3167-8.
  • 5Sartorius N. The economic and social burden of depres- sion. J Clin Psychiatry, 2001, 62(Suppl 15): 8-11.
  • 6Mathers CD, Loncar D. Projections of global mortality and burden of disease from 2002 to 2030. PLoS Med, 2006, 3(11): e442.
  • 7Schildkraut JJ. The catecholamine hypothesis of affective disorders: a review of supporting evidence. Am J Psychia- try, 1965, 122(5): 509-22.
  • 8Shabel S J, Proulx CD, Piriz J, et al. GABA/glutamate co-release controls habenula output and is modified by an- tidepressant treatment. Science, 2014, 345(6203): 1494-8.
  • 9Proulx CD, Hikosaka O, Malinow R. Reward processing by the lateral habenula in normal and depressive behav- iors. Nat Neurosci, 2014, 17(9): 1146-52.
  • 10Krishnan V, Nestler EJ. The molecular neurobiology of depression. Nature, 2008, 455(7215): 894-902.

同被引文献72

引证文献9

二级引证文献72

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部