A Translational Rodent Assay of Affective Biases in Depression and Antidepressant Therapy

被引:0
|
作者
Sarah A Stuart
Paul Butler
Marcus R Munafò
David J Nutt
Emma SJ Robinson
机构
[1] School of Physiology and Pharmacology,Division of Experimental Medicine
[2] University of Bristol,undefined
[3] University Walk,undefined
[4] Bristol,undefined
[5] UK,undefined
[6] Global Safety Pharmacology,undefined
[7] Pfizer Worldwide Research and Development,undefined
[8] School of Experimental Psychology,undefined
[9] University of Bristol,undefined
[10] Neuropsychopharmacology Unit,undefined
[11] Imperial College,undefined
[12] Burlington Danes Building,undefined
[13] Hammersmith Hospital,undefined
来源
Neuropsychopharmacology | 2013年 / 38卷
关键词
depression; antidepressant; pro-depressant; affective bias; animal model;
D O I
暂无
中图分类号
学科分类号
摘要
The subjective measures used to study mood disorders in humans cannot be replicated in animals; however, the increasing application of objective neuropsychological methods provides opportunities to develop translational animal tasks. Here we describe a novel behavioral approach, which has enabled us to investigate similar affective biases in rodents. In our affective bias test (ABT), rats encounter two independent positive experiences—the association between food reward and specific digging substrate—during discrimination learning sessions. These are performed on separate days under either neutral conditions or during a pharmacological or affective state manipulation. Affective bias is then quantified using a preference test where both previously rewarded substrates are presented together and the rat’s choices recorded. The absolute value of the experience is kept consistent and all other factors are counterbalanced so that any bias at recall can be attributed to treatment. Replicating previous findings from studies in healthy volunteers, we observe significant positive affective biases following acute treatment with typical (fluoxetine, citalopram, reboxetine, venlafaxine, clomipramine) and atypical antidepressants (agomelatine, mirtazapine), and significant negative affective biases following treatment with drugs associated with inducing negative affective states in humans (FG7142, rimonabant, 13-cis retinoic acid). We also observed that acute psychosocial stress and environmental enrichment induce significant negative and positive affective biases, respectively, and provide evidence that these affective biases involve memory consolidation. The positive and negative affective biases induced in our test also mirror the antidepressant and pro-depressant effects of these drugs in patients suggesting our test has both translational and predictive validity. Our results suggest that cognitive affective biases could contribute to drug- or stress-induced mood changes in people and support the hypothesis that a cognitive neuropsychological mechanism contributes to antidepressant drug efficacy.
引用
收藏
页码:1625 / 1635
页数:10
相关论文
共 50 条
  • [31] Depression Cardiovascular Risks of Antidepressant-Therapy
    Klein, Friederike
    FORTSCHRITTE DER NEUROLOGIE PSYCHIATRIE, 2016, 84 (06) : 333 - 333
  • [32] Antidepressant therapy in a post-stroke depression
    Starkstein, Sergio E.
    Mizrahi, Romina
    Power, Brian D.
    EXPERT OPINION ON PHARMACOTHERAPY, 2008, 9 (08) : 1291 - 1298
  • [33] The Effects of Neurofeedback Training of Salience Network Nodes on Affective Biases in Major Depression
    Sacchet, Matthew D.
    Hamilton, J. Paul
    Glover, Gary H.
    Bagarinao, Epifanio
    Chang, Catie
    Mackey, Sean
    Gotlib, Ian H.
    BIOLOGICAL PSYCHIATRY, 2013, 73 (09) : 220S - 220S
  • [34] Affective Processing Biases in Relation to Past, Current, and Future Depression in Children and Adolescents
    Salem, Taban
    Fristad, Mary A.
    Arnold, L. Eugene
    Taylor, H. Gerry
    Frazier, Thomas W.
    Horwitz, Sarah M.
    Findling, Robert L.
    JOURNAL OF AFFECTIVE DISORDERS, 2020, 273 : 146 - 156
  • [35] Antidepressant Effects of Ketamine and Buprenorphine in a Rodent Model of LPS-Induced Depression
    Browne, Caroline
    Carabelli, Bruno
    Kalkhoran, Aylar Berenji
    Gouty, Kaitlyn
    Aiyer, Sahana
    Lucki, Irwin
    NEUROPSYCHOPHARMACOLOGY, 2017, 42 : S161 - S161
  • [36] Antidepressant-Like Effect and Mechanism of Ginsenoside Rd on Rodent Models of Depression
    Li, Yu
    Wang, Mei-Ling
    Zhang, Bo
    Fan, Xiao-Xu
    Tang, Qin
    Yu, Xue
    Li, Li-Na
    Fan, Ang-Ran
    Chang, Hong-Sheng
    Zhang, Lan-Zhen
    DRUG DESIGN DEVELOPMENT AND THERAPY, 2022, 16 : 843 - 861
  • [37] Potential Antidepressant Mechanism of Quetiapine in the Chronic Mild Stress Rodent Model of Depression
    Moreines, Jared
    Owrutsky, Zoe
    Grace, Anthony
    NEUROPSYCHOPHARMACOLOGY, 2016, 41 : S302 - S303
  • [38] Pavlovian Biases in Depression: From Choice to Thought and Therapy
    Huys, Quentin
    Berwian, Isabel M.
    Wenzel, Julia
    Russek, Evan
    Abitante, George
    Schnuerer, Inga
    Kuehn, Leonie
    Seifritz, Erich
    Stephan, Klaas
    Gollan, Jacqueline
    Walter, Henrik
    BIOLOGICAL PSYCHIATRY, 2020, 87 (09) : S20 - S20
  • [39] The functional neuroanatomy of affective and cognitive changes associated with antidepressant treatment in geriatric depression
    Kahn, Alan S.
    Kramer, Elisse
    Hermann, Carol R.
    Hanratty, M. Katherine
    Ma, Yilong
    Eidelberg, David
    Smith, Gwenn S.
    BIOLOGICAL PSYCHIATRY, 2008, 63 (07) : 205S - 205S
  • [40] Early antidepressant response of deep brain stimulation for depression treatment: a translational study
    Perez-Caballero, L.
    Perez-Egea, R.
    Puigdemont, D.
    Molet, J.
    Mico, J. A.
    Perez, V.
    Berrocoso, E.
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2011, 21 : S445 - S446