Mathew Sanjay J, Manji Husseini K, Charney Dennis S
Mood and Anxiety Disorders Program, Department of Psychiatry, Mount Sinai School of Medicine, New York, NY 10029, USA.
Neuropsychopharmacology. 2008 Aug;33(9):2080-92. doi: 10.1038/sj.npp.1301652. Epub 2008 Jan 2.
Monoaminergic-based drugs remain the primary focus of pharmaceutical industry drug discovery efforts for mood disorders, despite serious limitations regarding their ability to achieve remission. The quest for novel therapies for unipolar depression and bipolar disorder has generally centered on two complementary approaches: (1) understanding the presumed therapeutically relevant biochemical targets of currently available medications, and using that knowledge to design new drugs directed at both direct biochemical targets and downstream targets that are regulated by chronic drug administration; and (2) developing pathophysiological models of the illness to design therapeutics to attenuate or prevent those pathological processes. This review describes several promising drugs and drug targets for mood disorders using one or both of these approaches. Agents interacting with non-catecholamine neurotransmitter systems with particular promise for unipolar and bipolar depression include excitatory amino acid neurotransmitter modulators (eg, riluzole, N-methyl-D-aspartate antagonists, and AMPA receptor potentiators) and neuropeptide antagonists (targeting corticotropin releasing factor-1 and neurokinin receptors). Potential antidepressant and mood-stabilizing agents targeting common intracellular pathways of known monoaminergic agents and lithium/mood stabilizers are also reviewed, such as neurotrophic factors, extracellular receptor-coupled kinase (ERK) mitogen-activated protein (MAP) kinase and the bcl-2 family of proteins, and inhibitors of phosphodiesterase, glycogen synthase kinase-3, and protein kinase C. A major thrust of drug discovery in mood disorders will continue efforts to identify agents with rapid and sustained onsets of action (such as intravenous administration of ketamine), as well as identify drugs used routinely in non-psychiatric diseases for their antidepressant and mood-stabilizing properties.
尽管基于单胺能的药物在实现缓解方面存在严重局限性,但它们仍然是制药行业治疗情绪障碍药物研发工作的主要重点。针对单相抑郁症和双相情感障碍的新型疗法探索通常集中在两种互补方法上:(1)了解现有药物假定的治疗相关生化靶点,并利用这些知识设计针对直接生化靶点和由长期药物给药调节的下游靶点的新药;(2)建立疾病的病理生理模型,以设计治疗方法来减轻或预防这些病理过程。本综述使用上述一种或两种方法描述了几种治疗情绪障碍的有前景的药物和药物靶点。与非儿茶酚胺神经递质系统相互作用且对单相和双相抑郁症特别有前景的药物包括兴奋性氨基酸神经递质调节剂(如利鲁唑、N-甲基-D-天冬氨酸拮抗剂和α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体增强剂)和神经肽拮抗剂(靶向促肾上腺皮质激素释放因子-1和神经激肽受体)。还综述了针对已知单胺能药物和锂盐/心境稳定剂常见细胞内途径的潜在抗抑郁药和心境稳定剂,如神经营养因子、细胞外受体偶联激酶(ERK)丝裂原活化蛋白(MAP)激酶和bcl-2蛋白家族,以及磷酸二酯酶、糖原合酶激酶-3和蛋白激酶C的抑制剂。情绪障碍药物研发的一个主要方向将继续努力寻找起效迅速且持续的药物(如静脉注射氯胺酮),以及确定在非精神疾病中常规使用且具有抗抑郁和心境稳定特性的药物。