Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Mexico City 04510, Mexico.
Department of Neuroscience, Karolinska Institutet, Biomedicum, Solnavägen 9., 17177 Stockholm, Sweden.
Cells. 2022 Jun 2;11(11):1826. doi: 10.3390/cells11111826.
Among mental diseases, major depressive disorder (MDD) and anxiety deserve a special place due to their high prevalence and their negative impact both on society and patients suffering from these disorders. Consequently, the development of novel strategies designed to treat them quickly and efficiently, without or at least having limited side effects, is considered a highly important goal. Growing evidence indicates that emerging properties are developed on recognition, trafficking, and signaling of G-protein coupled receptors (GPCRs) upon their heteromerization with other types of GPCRs, receptor tyrosine kinases, and ionotropic receptors such as N-methyl-D-aspartate (NMDA) receptors. Therefore, to develop new treatments for MDD and anxiety, it will be important to identify the most vulnerable heteroreceptor complexes involved in MDD and anxiety. This review focuses on how GPCRs, especially serotonin, dopamine, galanin, and opioid heteroreceptor complexes, modulate synaptic and volume transmission in the limbic networks of the brain. We attempt to provide information showing how these emerging concepts can contribute to finding new ways to treat both MDD and anxiety disorders.
在精神疾病中,由于其高患病率以及对社会和患有这些疾病的患者的负面影响,重度抑郁症(MDD)和焦虑症应占据特殊地位。因此,开发旨在快速有效地治疗这些疾病的新策略,而没有或至少具有有限的副作用,被认为是一个非常重要的目标。越来越多的证据表明,在 G 蛋白偶联受体(GPCR)与其他类型的 GPCR、受体酪氨酸激酶和离子型受体(如 N-甲基-D-天冬氨酸(NMDA)受体)异源三聚化时,其识别、运输和信号转导方面出现了新的特性。因此,为了开发治疗 MDD 和焦虑症的新方法,确定与 MDD 和焦虑症相关的最脆弱的异源受体复合物将非常重要。这篇综述重点介绍了 GPCR 如何调节大脑边缘网络中的突触和容积传递,特别是 5-羟色胺、多巴胺、甘丙肽和阿片类异源受体复合物。我们试图提供信息,表明这些新出现的概念如何有助于寻找治疗 MDD 和焦虑症的新方法。