Dysfunctional Heteroreceptor Complexes as Novel Targets for the Treatment of Major Depressive and Anxiety Disorders
Miguel Pérez de la Mora,
Dasiel O. Borroto-Escuela,
Minerva Crespo-Ramírez,
José del Carmen Rejón-Orantes,
Daniel Alejandro Palacios-Lagunas,
Magda K. Martínez-Mata,
Daniela Sánchez-Luna,
Emiliano Tesoro-Cruz,
Kjell Fuxe
Affiliations
Miguel Pérez de la Mora
Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Mexico City 04510, Mexico
Dasiel O. Borroto-Escuela
Department of Neuroscience, Karolinska Institutet, Biomedicum, Solnavägen 9., 17177 Stockholm, Sweden
Minerva Crespo-Ramírez
Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Mexico City 04510, Mexico
José del Carmen Rejón-Orantes
Laboratorio Experimental de Farmacobiología, Facultad de Medicina Humana C-II, Universidad Autónoma de Chiapas, Tuxtla Gutiérrez 29026, Mexico
Daniel Alejandro Palacios-Lagunas
Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Mexico City 04510, Mexico
Magda K. Martínez-Mata
Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Mexico City 04510, Mexico
Daniela Sánchez-Luna
Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Mexico City 04510, Mexico
Emiliano Tesoro-Cruz
Unidad de Investigación Biomédica en Inmunología e Infectología, Hospital de Infectología, Centro Médico Nacional La Raza, IMSS, Mexico City 01000, Mexico
Kjell Fuxe
Department of Neuroscience, Karolinska Institutet, Biomedicum, Solnavägen 9., 17177 Stockholm, Sweden
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.