Literature DB >> 12882315

The circadian Clock mutation increases exploratory activity and escape-seeking behavior.

A Easton1, J Arbuzova, F W Turek.   

Abstract

Disturbances of circadian rhythms are associated with many types of mood disorders; however, it is unknown whether a dysfunctional circadian pacemaker can be the primary cause of altered emotional behavior. To test this hypothesis, male and female mice carrying a mutation of the circadian gene, Clock, were compared to wild-type mice in an array of behavioral tests used to measure exploratory activity, anxiety, and behavioral despair. Female Clock mutant mice exhibited significantly greater activity and rearing in an open field and a greater number of total arm entries in the elevated plus maze. In addition, female Clock mutant mice spent significantly more time swimming in the forced swim test than wild-type mice on both days of a 2-day test. Male Clock mutant mice also exhibited increased exploration of the open field and increased swimming in the forced swim test; however, behavioral changes were less robust in Clock mutant males compared to Clock mutant females. These changes in behavior were not dependent on the expression of a lengthened free-running period but were more or less striking depending on the testing conditions. These data indicate that the Clock mutation leads to increased exploratory behavior and increased escape-seeking behavior, and, conversely, does not result in increased anxiety or depressive-like behavior. These results suggest that the Clock gene is involved in regulating behavioral arousal, and that Clock may interact with sex hormones to produce these behavioral changes.

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Year:  2003        PMID: 12882315     DOI: 10.1034/j.1601-183x.2003.00002.x

Source DB:  PubMed          Journal:  Genes Brain Behav        ISSN: 1601-183X            Impact factor:   3.449


  37 in total

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Review 4.  Forced swimming test in mice: a review of antidepressant activity.

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Review 5.  Circadian genes, rhythms and the biology of mood disorders.

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6.  Altered GluA1 (Gria1) Function and Accumbal Synaptic Plasticity in the ClockΔ19 Model of Bipolar Mania.

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7.  Biochemical, molecular and behavioral phenotypes of Rab3A mutations in the mouse.

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Journal:  Genes Brain Behav       Date:  2007-02       Impact factor: 3.449

8.  Behavioral changes and dopaminergic dysregulation in mice lacking the nuclear receptor Rev-erbα.

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9.  Circadian clock proteins control adaptation to novel environment and memory formation.

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Journal:  Aging (Albany NY)       Date:  2010-05       Impact factor: 5.682

Review 10.  Face and predictive validity of the ClockΔ19 mouse as an animal model for bipolar disorder: a systematic review.

Authors:  M Kristensen; A A Nierenberg; S D Østergaard
Journal:  Mol Psychiatry       Date:  2017-11-07       Impact factor: 15.992

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