4.7 Review

Modelling cognitive affective biases in major depressive disorder using rodents

Journal

BRITISH JOURNAL OF PHARMACOLOGY
Volume 171, Issue 20, Pages 4524-4538

Publisher

WILEY
DOI: 10.1111/bph.12603

Keywords

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Funding

  1. BBSRC Industrial CASE studentship
  2. Pfizer, UK
  3. BBSRC studentship
  4. RCUK academic fellowship
  5. British Pharmacological Society Integrative Pharmacology Fund
  6. Medical Research Council
  7. Wellcome Trust [084621/Z/08/Z]
  8. BBSRC [BB/L009137/1] Funding Source: UKRI
  9. MRC [MR/L011212/1, G0700980] Funding Source: UKRI
  10. Biotechnology and Biological Sciences Research Council [BB/L009137/1] Funding Source: researchfish
  11. Medical Research Council [MR/L011212/1, G0700980] Funding Source: researchfish
  12. Wellcome Trust [084621/Z/08/Z] Funding Source: Wellcome Trust

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Major depressive disorder (MDD) affects more than 10% of the population, although our understanding of the underlying aetiology of the disease and how antidepressant drugs act to remediate symptoms is limited. Major obstacles include the lack of availability of good animal models that replicate aspects of the phenotype and tests to assay depression-like behaviour in non-human species. To date, research in rodents has been dominated by two types of assays designed to test for depression-like behaviour: behavioural despair tests, such as the forced swim test, and measures of anhedonia, such as the sucrose preference test. These tests have shown relatively good predictive validity in terms of antidepressant efficacy, but have limited translational validity. Recent developments in clinical research have revealed that cognitive affective biases (CABs) are a key feature of MDD. Through the development of neuropsychological tests to provide objective measures of CAB in humans, we have the opportunity to use 'reverse translation' to develop and evaluate whether similar methods are suitable for research into MDD using animals. The first example of this approach was reported in 2004 where rodents in a putative negative affective state were shown to exhibit pessimistic choices in a judgement bias task. Subsequent work in both judgement bias tests and a novel affective bias task suggest that these types of assay may provide translational methods for studying MDD using animals. This review considers recent work in this area and the pharmacological and translational validity of these new animal models of CABs.

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