Müller Marianne B, Wurst Wolfgang
Max Planck Institute of Psychiatry, Kraepelinstrasse 2-10, 80804 Munich, Germany.
Trends Mol Med. 2004 Aug;10(8):409-15. doi: 10.1016/j.molmed.2004.06.007.
Depressive disorders are a leading cause of morbidity and mortality worldwide. Current antidepressant drugs targeting monoamine neurotransmitter systems have a delayed onset of action, and fewer than 50% of the patients attain complete remission after therapy with a single antidepressant. A large body of preclinical and clinical evidence points to a key role of the corticotropin-releasing hormone (CRH) receptor 1 subtype (CRHR1) in mediating CRH-elicited effects in anxiety, depressive disorders and stress-associated pathologies. Genetic modification of CRHR1 function in mice by the use of conventional and conditional knockout strategies enables further analysis of specific elements in the CRH circuitry. The recent characterisation of several selective small-molecule CRHR1 antagonists offers new possibilities for the treatment of anxiety and depression.
抑郁症是全球发病和死亡的主要原因。目前针对单胺神经递质系统的抗抑郁药物起效延迟,且单一抗抑郁药物治疗后不到50%的患者能实现完全缓解。大量临床前和临床证据表明,促肾上腺皮质激素释放激素(CRH)受体1亚型(CRHR1)在介导CRH引发的焦虑、抑郁障碍及应激相关病症中起关键作用。通过常规和条件性基因敲除策略对小鼠CRHR1功能进行基因改造,有助于进一步分析CRH信号通路中的特定元件。最近几种选择性小分子CRHR1拮抗剂的特性为焦虑症和抑郁症的治疗提供了新的可能性。