New translational assays for preclinical modelling of cognition in schizophrenia: The touchscreen testing method for mice and rats

We describe a touchscreen method that satisfies a proposed ‘wish-list’ of desirables for a cognitive testing method for assessing rodent models of schizophrenia. A number of tests relevant to schizophrenia research are described which are currently being developed and validated using this method. Th...

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Published inNeuropharmacology Vol. 62; no. 3; pp. 1191 - 1203
Main Authors Bussey, T.J., Holmes, A., Lyon, L., Mar, A.C., McAllister, K.A.L., Nithianantharajah, J., Oomen, C.A., Saksida, L.M.
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.03.2012
Subjects
Animals
Attention
Autoshaping
Cognition
Cognition Disorders - physiopathology
Cognition Disorders - psychology
Computers
Discrimination, Psychological
Disease Models, Animal
Extinction
Mice
Neurogenesis
Neuropsychological Tests
Paired associate learning
Pattern separation
PCP
Photic Stimulation
Psychomotor Performance
Rats
Schizophrenia - physiopathology
Schizophrenic Psychology
Touch
Translational Research, Biomedical - methods
Visual discrimination
Working memory
Extinction
Pattern separation
Attention
Paired associate learning
Autoshaping
Cognition
Working memory
PCP
Visual discrimination
Neurogenesis
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Abstract We describe a touchscreen method that satisfies a proposed ‘wish-list’ of desirables for a cognitive testing method for assessing rodent models of schizophrenia. A number of tests relevant to schizophrenia research are described which are currently being developed and validated using this method. These tests can be used to study reward learning, memory, perceptual discrimination, object-place associative learning, attention, impulsivity, compulsivity, extinction, simple Pavlovian conditioning, and other constructs. The tests can be deployed using a ‘flexible battery’ approach to establish a cognitive profile for a particular mouse or rat model. We have found these tests to be capable of detecting not just impairments in function, but enhancements as well, which is essential for testing putative cognitive therapies. New tests are being continuously developed, many of which may prove particularly valuable for schizophrenia research. This article is part of a Special Issue entitled ‘Schizophrenia’. ► We describe a touchscreen method for assaying cognition in rodent models. ► A number of tests relevant to schizophrenia research are described. ► The tests can be used to study multiple aspects of cognition. ► The tests can be combined in a flexible battery to establish a cognitive profile. ► The tests are capable of detecting both impairments and enhancements in function.
AbstractList We describe a touchscreen method that satisfies a proposed 'wish-list' of desirables for a cognitive testing method for assessing rodent models of schizophrenia. A number of tests relevant to schizophrenia research are described which are currently being developed and validated using this method. These tests can be used to study reward learning, memory, perceptual discrimination, object-place associative learning, attention, impulsivity, compulsivity, extinction, simple Pavlovian conditioning, and other constructs. The tests can be deployed using a 'flexible battery' approach to establish a cognitive profile for a particular mouse or rat model. We have found these tests to be capable of detecting not just impairments in function, but enhancements as well, which is essential for testing putative cognitive therapies. New tests are being continuously developed, many of which may prove particularly valuable for schizophrenia research.
We describe a touchscreen method that satisfies a proposed ‘wish-list’ of desirables for a cognitive testing method for assessing rodent models of schizophrenia. A number of tests relevant to schizophrenia research are described which are currently being developed and validated using this method. These tests can be used to study reward learning, memory, perceptual discrimination, object-place associative learning, attention, impulsivity, compulsivity, extinction, simple Pavlovian conditioning, and other constructs. The tests can be deployed using a ‘flexible battery’ approach to establish a cognitive profile for a particular mouse or rat model. We have found these tests to be capable of detecting not just impairments in function, but enhancements as well, which is essential for testing putative cognitive therapies. New tests are being continuously developed, many of which may prove particularly valuable for schizophrenia research. This article is part of a Special Issue entitled ‘Schizophrenia’. ► We describe a touchscreen method for assaying cognition in rodent models. ► A number of tests relevant to schizophrenia research are described. ► The tests can be used to study multiple aspects of cognition. ► The tests can be combined in a flexible battery to establish a cognitive profile. ► The tests are capable of detecting both impairments and enhancements in function.
Author Nithianantharajah, J.
Lyon, L.
Saksida, L.M.
Holmes, A.
McAllister, K.A.L.
Oomen, C.A.
Bussey, T.J.
Mar, A.C.
AuthorAffiliation 3 National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, 5625 Fishers Lane, Room 2N09 Rockville MD 20852-9411
4 Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge. CB10 1SA UK
1 Department of Experimental Psychology, University of Cambridge, Downing St., Cambridge CB2 3EB, UK
2 The MRC and Wellcome Trust Behavioural and Clinical Neuroscience Institute, University of Cambridge, Downing St., Cambridge CB2 3EB, UK
AuthorAffiliation_xml – name: 4 Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge. CB10 1SA UK
– name: 1 Department of Experimental Psychology, University of Cambridge, Downing St., Cambridge CB2 3EB, UK
– name: 2 The MRC and Wellcome Trust Behavioural and Clinical Neuroscience Institute, University of Cambridge, Downing St., Cambridge CB2 3EB, UK
– name: 3 National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, 5625 Fishers Lane, Room 2N09 Rockville MD 20852-9411
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  fullname: Bussey, T.J.
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  fullname: Holmes, A.
  organization: National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, 5625 Fishers Lane, Room 2N09, Rockville, MD 20852-9411, USA
– sequence: 3
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  surname: Lyon
  fullname: Lyon, L.
  organization: Department of Experimental Psychology, University of Cambridge, Downing Street, Cambridge CB2 3EB, UK
– sequence: 4
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  surname: Mar
  fullname: Mar, A.C.
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– sequence: 5
  givenname: K.A.L.
  surname: McAllister
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– sequence: 6
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  surname: Nithianantharajah
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  givenname: L.M.
  surname: Saksida
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/21530550$$D View this record in MEDLINE/PubMed
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Issue 3
Keywords Extinction
Pattern separation
Attention
Paired associate learning
Autoshaping
Cognition
Working memory
PCP
Visual discrimination
Neurogenesis
Language English
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Snippet We describe a touchscreen method that satisfies a proposed ‘wish-list’ of desirables for a cognitive testing method for assessing rodent models of...
We describe a touchscreen method that satisfies a proposed 'wish-list' of desirables for a cognitive testing method for assessing rodent models of...
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SubjectTerms Animals
Attention
Autoshaping
Cognition
Cognition Disorders - physiopathology
Cognition Disorders - psychology
Computers
Discrimination, Psychological
Disease Models, Animal
Extinction
Mice
Neurogenesis
Neuropsychological Tests
Paired associate learning
Pattern separation
PCP
Photic Stimulation
Psychomotor Performance
Rats
Schizophrenia - physiopathology
Schizophrenic Psychology
Touch
Translational Research, Biomedical - methods
Visual discrimination
Working memory
Title New translational assays for preclinical modelling of cognition in schizophrenia: The touchscreen testing method for mice and rats
URI https://dx.doi.org/10.1016/j.neuropharm.2011.04.011
https://www.ncbi.nlm.nih.gov/pubmed/21530550
https://search.proquest.com/docview/917576318
https://search.proquest.com/docview/923194252
https://pubmed.ncbi.nlm.nih.gov/PMC3168710
Volume 62
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