Disturbances of diurnal phase markers, behavior, and clock genes in a rat model of depression; modulatory effects of agomelatine treatment

K. Højgaard, S. L. Christiansen, E. V. Bouzinova, O. Wiborg*

*Kontaktforfatter

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

8 Citationer (Scopus)

Abstract

Major depressive disorder (MDD) is a growing problem worldwide. Though, the etiology remains unresolved, circadian rhythm disturbances are frequently observed in MDD and thus is speculated to play a key role herein. The present study focuses on circadian rhythm disturbances in the chronic mild stress (CMS) animal model of depression and examined whether the atypical antidepressant, agomelatine, which is mediating its action via melatonergic and serotonergic receptors, is capable of resynchronizing the perturbed rhythm. Melatonin is often used as a marker of the circadian phase, but the functional and behavioral output is dictated on a cellular level by the molecular clock, driven by the clock genes. We applied in situ hybridization histochemistry to measure the expression levels of the core clock genes, period (Per) 1 and 2 and bone and muscle ARNT-like protein 1 (Bmal1), in multiple brain regions believed to be implicated in depression. Agomelatine showed an antidepressant-like effect in the sucrose consumption test and an anxiolytic-like profile in the elevated zero maze. We found that CMS increased nighttime melatonin release in rats and that agomelatine attenuated this effect. Stress was shown to have a time and region-specific effect on clock gene expression in the brain. Treatment with agomelatine failed to normalize clock gene expression, and the observed modifying effect on gene expression did not associate with the antidepressant-like effect. This suggests that the antidepressant actions of agomelatine are mainly independent of circadian rhythm synchronization and, in this regard, not superior to traditional antidepressants tested in our model.

OriginalsprogEngelsk
TidsskriftPsychopharmacology
Vol/bind235
Udgave nummer3
Sider (fra-til)627-640
Antal sider14
ISSN0033-3158
DOI
StatusUdgivet - 1 mar. 2018
Udgivet eksterntJa

Bibliografisk note

Funding Information:
We thank Jan Fahrenkrug and Jens Hannibal from Department of Clinical Medicine, Bispebjerg-Frederiksberg Hospital, Copenhagen, for their valuable help with in situ hybridization histochemistry.

Publisher Copyright:
© 2017, Springer-Verlag GmbH Germany, part of Springer Nature.

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