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Comprehensive behavioral analysis of voltage-gated calcium channel beta-anchoring and -regulatory protein knockout mice.

Front Behav Neurosci. 2015 Jun 16;9:141. doi:10.3389/fnbeh.2015.00141. eCollection 2015
Akito Nakao 1 , Takafumi Miki 2 , Hirotaka Shoji 3 , Miyuki Nishi 4 , Hiroshi Takeshima 4 , Tsuyoshi Miyakawa 5 , Yasuo Mori 2
Akito Nakao 1 , Takafumi Miki 2 , Hirotaka Shoji 3 , Miyuki Nishi 4 , Hiroshi Takeshima 4 , Tsuyoshi Miyakawa 5 , Yasuo Mori 2
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Author information
  • 1 Division of Systems Medical Science, Institute for Comprehensive Medical Science, Fujita Health University Toyoake, Japan.
  • 2 Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University Kyoto, Japan.
  • 3 Division of Systems Medical Science, Institute for Comprehensive Medical Science, Fujita Health University Toyoake, Japan ; Japan Science and Technology Agency, Core Research for Evolutional Science and Technology Kawaguchi, Japan.
  • 4 Department of Biological Chemistry, Graduate School of Pharmaceutical Sciences, Kyoto University Kyoto, Japan.
  • 5 Division of Systems Medical Science, Institute for Comprehensive Medical Science, Fujita Health University Toyoake, Japan ; Japan Science and Technology Agency, Core Research for Evolutional Science and Technology Kawaguchi, Japan ; Section of Behavior Patterns, Center for Genetic Analysis of Behavior, National Institute for Physiological Sciences Okazaki, Japan.
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摘要


Calcium (Ca(2+)) influx through voltage-gated Ca(2+) channels (VGCCs) induces numerous intracellular events such as neuronal excitability, neurotransmitter release, synaptic plasticity, and gene regulation. It has been shown that genes related to Ca(2+) signaling, such as the CACNA1C, CACNB2, and CACNA1I genes that encode VGCC subunits, are associated with schizophrenia and other psychiatric disorders. Recently, VGCC beta-anchoring and -regulatory protein was identified as a novel regulator of VGCC activity via the interaction of VGCC β subunits. To examine the role of the in higher brain functions, we generated Bduanyu37 knockout (KO) mice and conducted a comprehensive battery of behavioral tests. Bduanyu37 KO mice exhibited greatly reduced locomotor activity, as evidenced by decreased vertical activity, stereotypic counts in the open field test, and activity level in the home cage, and longer latency to complete a session in spontaneous T-maze alteration test, which reached "study-wide significance." Acoustic startle response was also reduced in the mutants. Interestingly, they showed multiple behavioral phenotypes that are seemingly opposite to those seen in the mouse models of schizophrenia and its related disorders, including increased working memory, flexibility, prepulse inhibition, and social interaction, and decreased locomotor activity, though many of these phenotypes are statistically weak and require further replications. These results demonstrate that Bduanyu37 is involved in the regulation of locomotor activity and, possibly, emotionality. The possibility was also suggested that Bduanyu37 KO mice may serve as a unique tool for investigating the pathogenesis/pathophysiology of schizophrenia and related disorders. Further evaluation of the molecular and physiological phenotypes of the mutant mice would provide new insights into the role of Bduanyu37 in higher brain functions.

KEYWORDS: behavior, knockout mouse, psychiatric disorders, voltage-gated calcium channel beta-anchoring and -regulatory protein, voltage-gated calcium channels