Catapano Lisa A, Manji Husseini K
Laboratory of Molecular Pathophysiology, Mood and Anxiety Disorders Program, National Institute of Mental Health, NIH, HHS, Bethesda, MD 20892, USA.
Biochim Biophys Acta. 2007 Apr;1768(4):976-93. doi: 10.1016/j.bbamem.2006.09.025. Epub 2006 Oct 3.
Although the molecular mechanisms underlying psychiatric illnesses such as depression, bipolar disorder and schizophrenia remain incompletely understood, there is increasing clinical, pharmacologic, and genetic evidence that G protein-coupled receptors (GPCRs) play critical roles in these disorders and their treatments. This perspectives paper reviews and synthesizes the available data. Dysfunction of multiple neurotransmitter and neuropeptide GPCRs in frontal cortex and limbic-related regions, such as the hippocampus, hypothalamus and brainstem, likely underlies the complex clinical picture that includes cognitive, perceptual, affective and motoric symptoms. The future development of novel agents targeting GPCR signaling cascades remains an exciting prospect for patients refractory to existing therapeutics.
尽管诸如抑郁症、双相情感障碍和精神分裂症等精神疾病背后的分子机制仍未完全明了,但越来越多的临床、药理学和遗传学证据表明,G蛋白偶联受体(GPCRs)在这些疾病及其治疗中发挥着关键作用。这篇观点文章回顾并综合了现有数据。额叶皮质以及与边缘系统相关区域(如海马体、下丘脑和脑干)中多种神经递质和神经肽GPCRs的功能障碍,可能是导致包括认知、感知、情感和运动症状在内的复杂临床症状的基础。对于现有治疗方法难治的患者而言,靶向GPCR信号级联反应的新型药物的未来研发仍是一个令人兴奋的前景。