Animal models of major depression: drawbacks and challenges.


Journal

Journal of neural transmission (Vienna, Austria : 1996)
ISSN: 1435-1463
Titre abrégé: J Neural Transm (Vienna)
Pays: Austria
ID NLM: 9702341

Informations de publication

Date de publication:
11 2019
Historique:
received: 25 06 2019
accepted: 17 09 2019
pubmed: 5 10 2019
medline: 25 8 2020
entrez: 5 10 2019
Statut: ppublish

Résumé

Major depression is a leading contributor to the global burden of disease. This situation is mainly related to the chronicity and/or recurrence of the disorder, and to poor response to antidepressant therapy. Progress in this area requires valid animal models. Current models are based either on manipulating the environment to which rodents are exposed (during the developmental period or adulthood) or biological underpinnings (i.e. gene deletion or overexpression of candidate genes, targeted lesions of brain areas, optogenetic control of specific neuronal populations, etc.). These manipulations can alter specific behavioural and biological outcomes that can be related to different symptomatic and pathophysiological dimensions of major depression. However, animal models of major depression display substantial shortcomings that contribute to the lack of innovative pharmacological approaches in recent decades and which hamper our capabilities to investigate treatment-resistant depression. Here, we discuss the validity of these models, review putative models of treatment-resistant depression, major depression subtypes and recurrent depression. Furthermore, we identify future challenges regarding new paradigms such as those proposing dimensional rather than categorical approaches to depression.

Identifiants

pubmed: 31584111
doi: 10.1007/s00702-019-02084-y
pii: 10.1007/s00702-019-02084-y
pmc: PMC6815270
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1383-1408

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Auteurs

Barbara Planchez (B)

UMR 1253, iBrain, Université de Tours, Inserm, Tours, France.

Alexandre Surget (A)

UMR 1253, iBrain, Université de Tours, Inserm, Tours, France.

Catherine Belzung (C)

UMR 1253, iBrain, Université de Tours, Inserm, Tours, France. catherine.belzung@univ-tours.fr.
UMR 1253, iBrain, UFR Sciences et Techniques, Parc Grandmont, 37200, Tours, France. catherine.belzung@univ-tours.fr.

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