Literature DB >> 33477830

Learned Immobility Produces Enduring Impairment of the HPA Axis Reactivity in Mice without Replicating the Broad Spectrum of Depressive-Like Phenotype.

Sébastien Bullich1, Sarah Delcourte2, Nasser Haddjeri2, Bruno P Guiard1.   

Abstract

The forced swim stress test (FST) is widely used for screening pharmacological or non-pharmacological strategies with potential antidepressant activities. Recent data have suggested that repeated FST for five consecutive days (i.e., 5d-RFSS) could be used to generate a robust depressive-like phenotype in mice. However, the face, construct, and predictive validities of 5d-RFSS have been recently challenged. This study took advantage of recent findings showing that mice vulnerability to anxiety is enhanced when animals are stressed during the dark phase, to provide new insight into the relevance of this model. Our results showed a progressive increase in time of immobility in 5d-RFSS mice relative to control non-stressed animals (sham). Three weeks later, we noticed that 5d-RFSS mice injected with the vehicle compound (Veh) still exhibited a high level of immobility in the FST whereas this behavior was reversed by the antidepressant drug amitriptyline (AMI). However, 5d-RFSS/Veh and 5d-RFSS mice/AMI mice showed normal performances in the open field, the novelty suppressed feeding and the tail suspension tests. Despite this lack of generalized behavioral deficits, an impairment of different parameters characterizing the hypothalamic-pituitary-adrenal (HPA) axis reactivity was evidenced in 5d-RFSS mice/Veh but not in 5d-RFSS mice/AMI. Despite anomalies in the HPA axis, the activity of the central serotonergic system remained unaffected in 5d-RFSS mice relative to controls. From our results, it is suggested that learned immobility does not replicate the broad spectrum of depressive symptoms observed in other chronic models of depression such as the unpredictable chronic mild stress (UCMS) model, the chronic social defeat stress (CSDS) model or chronic corticosterone (CORT) exposure but its influence on the HPA axis is remarkable. Further experiments are warranted to makes this model suitable for modelling depression and therefore refine its translational applicability.

Entities:  

Keywords:  HPA axis; animal model; antidepressant; depression; forced swim stress; serotonin

Mesh:

Substances:

Year:  2021        PMID: 33477830      PMCID: PMC7832836          DOI: 10.3390/ijms22020937

Source DB:  PubMed          Journal:  Int J Mol Sci        ISSN: 1422-0067            Impact factor:   5.923


  49 in total

1.  Penetration of amitriptyline, but not of fluoxetine, into brain is enhanced in mice with blood-brain barrier deficiency due to mdr1a P-glycoprotein gene disruption.

Authors:  M Uhr; T Steckler; A Yassouridis; F Holsboer
Journal:  Neuropsychopharmacology       Date:  2000-04       Impact factor: 7.853

Review 2.  Neurobiological Mechanisms of Stress Resilience and Implications for the Aged Population.

Authors:  Charlene Faye; Josephine C Mcgowan; Christine A Denny; Denis J David
Journal:  Curr Neuropharmacol       Date:  2018-03-05       Impact factor: 7.363

3.  A Citrus Based Sensory Functional Food Ingredient Induces Antidepressant-like Effects: Possible Involvement of an Interplay between the Olfactory and the Serotonergic Systems.

Authors:  B Coutens; K Rekik; A Harster; P Etienne; V Noirot; B Frances; L Moulédous; B P Guiard
Journal:  Neuroscience       Date:  2020-10-09       Impact factor: 3.590

4.  Altered response to the selective serotonin reuptake inhibitor escitalopram in mice heterozygous for the serotonin transporter: an electrophysiological and neurochemical study.

Authors:  Bruno P Guiard; Mostafa El Mansari; Dennis L Murphy; Pierre Blier
Journal:  Int J Neuropsychopharmacol       Date:  2011-03-25       Impact factor: 5.176

5.  The effect of amitriptyline on inhibitory avoidance in mice is dose-dependent.

Authors:  Andrés Parra; Concepción Vinader-Caerols; Aránzazu Ferrer-Añó; Adoración Urquiza; Santiago Monleón
Journal:  Psicothema       Date:  2009-11

6.  Sex differences in response to oral amitriptyline in three animal models of depression in C57BL/6J mice.

Authors:  B J Caldarone; K Karthigeyan; A Harrist; J G Hunsberger; E Wittmack; S L King; P Jatlow; M R Picciotto
Journal:  Psychopharmacology (Berl)       Date:  2003-07-15       Impact factor: 4.530

Review 7.  Corticosteroid-serotonin interactions in the neurobiological mechanisms of stress-related disorders.

Authors:  Laurence Lanfumey; Raymond Mongeau; Charles Cohen-Salmon; Michel Hamon
Journal:  Neurosci Biobehav Rev       Date:  2008-04-29       Impact factor: 8.989

8.  Neurogenesis-dependent and -independent effects of fluoxetine in an animal model of anxiety/depression.

Authors:  Denis J David; Benjamin Adam Samuels; Quentin Rainer; Jing-Wen Wang; Douglas Marsteller; Indira Mendez; Michael Drew; Douglas A Craig; Bruno P Guiard; Jean-Philippe Guilloux; Roman P Artymyshyn; Alain M Gardier; Christophe Gerald; Irina A Antonijevic; E David Leonardo; René Hen
Journal:  Neuron       Date:  2009-05-28       Impact factor: 17.173

9.  Circadian abnormalities in a mouse model of high trait anxiety and depression.

Authors:  Irene Griesauer; Weifei Diao; Marianne Ronovsky; Immanuel Elbau; Simone Sartori; Nicolas Singewald; Daniela D Pollak
Journal:  Ann Med       Date:  2014-01-10       Impact factor: 4.709

10.  Learning and memory impairments in a neuroendocrine mouse model of anxiety/depression.

Authors:  Flavie Darcet; Indira Mendez-David; Laurent Tritschler; Alain M Gardier; Jean-Philippe Guilloux; Denis J David
Journal:  Front Behav Neurosci       Date:  2014-05-01       Impact factor: 3.558

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.