Novel Pathways in the Treatment of Major Depression: Focus on the Glutamatergic System.
Depressive disorders
NMDA
antidepressants
antipsychotics
glutamate
ketamine
mGluR
postsynaptic density.
Journal
Current pharmaceutical design
ISSN: 1873-4286
Titre abrégé: Curr Pharm Des
Pays: United Arab Emirates
ID NLM: 9602487
Informations de publication
Date de publication:
2019
2019
Historique:
received:
26
01
2019
accepted:
06
03
2019
pubmed:
14
3
2019
medline:
14
2
2020
entrez:
14
3
2019
Statut:
ppublish
Résumé
Depressive disorders represent protean psychiatric illnesses with heterogeneous clinical manifestations and a multitude of comorbidities leading to severe disability. In spite of decades of research on the pathophysiogenesis of these disorders, the wide variety of pharmacotherapies currently used to treat them is based on the modulation of monoamines, whose alteration has been considered the neurobiological foundation of depression, and consequently of its treatment. However, approximately one third to a half of patients respond partially or become refractory to monoamine-based therapies, thereby jeopardizing the therapeutic effectiveness in the real world of clinical practice. Recent scientific evidence has been pointing out the essential role of other biological systems beyond monoamines in the pathophysiology of depressive disorders, in particular, the glutamatergic neurotransmission. In the present review, we will discuss the most advanced knowledge on the involvement of glutamatergic system in the molecular mechanisms at the basis of depression pathophysiology, as well as the glutamate-based therapeutic strategies currently suggested to optimize depression treatment (e.g., ketamine). Finally, we will mention further "neurobiological targeted" approaches, based on glutamate system, with the purpose of promoting new avenues of investigation aiming at developing interventions that overstep the monoaminergic boundaries to improve depressive disorders therapy.
Identifiants
pubmed: 30864501
pii: CPD-EPUB-97243
doi: 10.2174/1381612825666190312102444
doi:
Substances chimiques
Excitatory Amino Acid Agents
0
Glutamic Acid
3KX376GY7L
Ketamine
690G0D6V8H
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
381-387Informations de copyright
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