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Altered circadian locomotor activity in APP23 mice: a model for BPSD disturbances

Authors

  • Ellen Vloeberghs,

    1. Laboratory of Neurochemistry & Behaviour, Born-Bunge Foundation, Department of Biomedical Sciences, University of Antwerp, Universiteitsplein 1, B-2610 Wilrijk, Belgium
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    • E.V. and D.V.D. contributed equally to this work.

  • Debby Van Dam,

    1. Laboratory of Neurochemistry & Behaviour, Born-Bunge Foundation, Department of Biomedical Sciences, University of Antwerp, Universiteitsplein 1, B-2610 Wilrijk, Belgium
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    • E.V. and D.V.D. contributed equally to this work.

  • Sebastiaan Engelborghs,

    1. Laboratory of Neurochemistry & Behaviour, Born-Bunge Foundation, Department of Biomedical Sciences, University of Antwerp, Universiteitsplein 1, B-2610 Wilrijk, Belgium
    2. Department of Neurology – Memory Clinic, Middelheim General Hospital, Antwerp, Belgium
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  • Guy Nagels,

    1. Laboratory of Neurochemistry & Behaviour, Born-Bunge Foundation, Department of Biomedical Sciences, University of Antwerp, Universiteitsplein 1, B-2610 Wilrijk, Belgium
    2. National MS centre, Melsbroek, Belgium
    3. Department of Neurology, University Hospital Antwerp, Belgium
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  • Matthias Staufenbiel,

    1. Novartis Institutes of Biomedical Research Basel, Basel, Switzerland
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  • Peter Paul De Deyn

    1. Laboratory of Neurochemistry & Behaviour, Born-Bunge Foundation, Department of Biomedical Sciences, University of Antwerp, Universiteitsplein 1, B-2610 Wilrijk, Belgium
    2. Department of Neurology – Memory Clinic, Middelheim General Hospital, Antwerp, Belgium
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Professor P. P. De Deyn, 1Laboratory of Neurochemistry & Behaviour, as above.
E-mail:peter.dedeyn@ua.ac.be

Abstract

Over the past decade, clinical Alzheimer's disease research has been challenged with an increased interest in noncognitive symptomatology, commonly referred to as behavioural and psychological signs and symptoms of dementia (BPSD). In accordance, major attention is being paid to behavioural alterations in the phenotyping of transgenic mouse models. Besides an age-dependent decline of cognitive functions, the APP23 model was previously shown to exhibit cage activity disturbances, reminiscent of diurnal rhythm disturbances in Alzheimer patients. To further scrutinize these observations, circadian patterns of horizontal locomotor activity were assessed in 3-, 6- and 12-month-old APP23 mice and wild-type littermates in a test paradigm continuously recording cage activity over a period ranging from 1 to 3 days. At the age of 3 months, APP23 profiles resembled the wild-type pattern to a large extent, although minor differences were already noticeable. Six-month-old APP23 mice displayed an altered activity profile with a first indication of increased activity during the second half of the active phase, reminiscent of sundowning behaviour in Alzheimer patients. This bimodal overnight activity pattern became even more evident at the age of 12 months. The APP23 model was therefore shown to display an age-dependent development of cage activity disturbances and sundowning-like behaviour. A comparison is made with actigraphic recordings of human Alzheimer patients exhibiting sundowning behaviour. This first report of diurnal rhythm disturbances and sundowning-like phenomena in a transgenic mouse model greatly adds to the validity of the APP23 model.

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