Berk M, Dodd S, Kauer-Sant'anna M, Malhi G S, Bourin M, Kapczinski F, Norman T
Department of Clinical and Biomedical Sciences, Barwon Health and The Geelong Clinic, University of Melbourne, Geelong, Victoria, Australia.
Acta Psychiatr Scand Suppl. 2007(434):41-9. doi: 10.1111/j.1600-0447.2007.01058.x.
Rational therapeutic development in bipolar is hampered by a lack of pathophysiological model. However, there is a wealth of converging data on the role of dopamine in bipolar disorder. This paper therefore examines the possibility of a dopamine hypothesis for bipolar disorder.
A literature search was conducted using standard search engines Embase, PyschLIT, PubMed and MEDLINE. In addition, papers and book chapters known to the authors were retrieved and examined for further relevant articles.
Collectively, in excess of 100 articles were reviewed from which approximately 75% were relevant to the focus of this paper.
Pharmacological models suggest a role of increased dopaminergic drive in mania and the converse in depression. In Parkinson's disease, administration of high-dose dopamine precursors can produce a 'maniform' picture, which switches into a depressive analogue on withdrawal. It is possible that in bipolar disorder there is a cyclical process, where increased dopaminergic transmission in mania leads to a secondary down regulation of dopaminergic receptor sensitivity over time. This may lead to a period of decreased dopaminergic transmission, corresponding with the depressive phase, and the repetition of the cycle. This model, if verified, may have implications for rational drug development.
双相情感障碍缺乏病理生理模型,这阻碍了合理的治疗开发。然而,关于多巴胺在双相情感障碍中的作用,有大量相互印证的数据。因此,本文探讨双相情感障碍多巴胺假说的可能性。
使用标准搜索引擎Embase、PyschLIT、PubMed和MEDLINE进行文献检索。此外,检索作者已知的论文和书籍章节,以查找更多相关文章。
共查阅了100多篇文章,其中约75%与本文重点相关。
药理学模型表明,多巴胺能驱动增加在躁狂中起作用,而在抑郁中则相反。在帕金森病中,给予高剂量多巴胺前体可产生“类躁狂”表现,停药后转变为类似抑郁的表现。在双相情感障碍中,可能存在一个循环过程,即躁狂期多巴胺能传递增加,随着时间推移导致多巴胺能受体敏感性继发性下调。这可能导致一段时间内多巴胺能传递减少,与抑郁期相对应,并使循环重复。该模型若得到验证,可能对合理的药物开发具有启示意义。