Fishberg Department of Neuroscience, Mount Sinai School of Medicine, NY 10029, USA.
Neuropharmacology. 2010 Mar-Apr;58(4-5):683-93. doi: 10.1016/j.neuropharm.2009.12.004. Epub 2009 Dec 17.
The need for newer compounds to treat depression is an ever-growing concern due to the enormous societal and financial ramifications of this disorder. Here, we review some of the candidate systems that could potentially be involved in depression, or an inherent resistance to depression termed resilience, and the numerous protein targets for these systems. A substantial body of literature provides strong evidence that neurotrophic factors, glutamate receptors, hypothalamic feeding peptides, nuclear hormone receptors, and epigenetic mechanisms, among others, will make for interesting targets when examining depressive behavior or resilience in preclinical models, and eventually clinical trials. Although some of these targets for depression already appear promising, new waves of more selective compounds for any molecular system should promote a better understanding of this complex disease and perhaps improved treatments.
由于这种疾病对社会和经济造成了巨大影响,因此需要寻找新的化合物来治疗抑郁症,这是一个日益增长的关注点。在这里,我们回顾了一些可能与抑郁症相关的候选系统,或者称为对抑郁症的固有抵抗力,称为韧性,以及这些系统的许多蛋白质靶标。大量文献提供了有力的证据,表明神经营养因子、谷氨酸受体、下丘脑喂养肽、核激素受体和表观遗传机制等,在研究临床前模型中的抑郁行为或韧性时,以及最终在临床试验中,都将成为有趣的靶标。尽管一些针对抑郁症的靶点已经显示出了前景,但对于任何分子系统的更具选择性的新一波化合物,应该可以促进对这种复杂疾病的更好理解,并可能改善治疗方法。