Literature DB >> 21525375

A novel instrumented multipeg running wheel system, Step-Wheel, for monitoring and controlling complex sequential stepping in mice.

Takashi Kitsukawa1, Masatoshi Nagata, Dai Yanagihara, Ryohei Tomioka, Hideko Utsumi, Yasuo Kubota, Takeshi Yagi, Ann M Graybiel, Tetsuo Yamamori.   

Abstract

Motor control is critical in daily life as well as in artistic and athletic performance and thus is the subject of intense interest in neuroscience. Mouse models of movement disorders have proven valuable for many aspects of investigation, but adequate methods for analyzing complex motor control in mouse models have not been fully established. Here, we report the development of a novel running-wheel system that can be used to evoke simple and complex stepping patterns in mice. The stepping patterns are controlled by spatially organized pegs, which serve as footholds that can be arranged in adjustable, ladder-like configurations. The mice run as they drink water from a spout, providing reward, while the wheel turns at a constant speed. The stepping patterns of the mice can thus be controlled not only spatially, but also temporally. A voltage sensor to detect paw touches is attached to each peg, allowing precise registration of footfalls. We show that this device can be used to analyze patterns of complex motor coordination in mice. We further demonstrate that it is possible to measure patterns of neural activity with chronically implanted tetrodes as the mice engage in vigorous running bouts. We suggest that this instrumented multipeg running wheel (which we name the Step-Wheel System) can serve as an important tool in analyzing motor control and motor learning in mice.

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Year:  2011        PMID: 21525375      PMCID: PMC3129737          DOI: 10.1152/jn.00139.2011

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  27 in total

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Journal:  J Neurosci Methods       Date:  2002-06-30       Impact factor: 2.390

Review 2.  The neural basis of temporal processing.

Authors:  Michael D Mauk; Dean V Buonomano
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Review 3.  What makes us tick? Functional and neural mechanisms of interval timing.

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4.  Abnormalities of motor timing in Huntington's disease.

Authors:  J S Freeman; F W Cody; D J O'Boyle; D Craufurd; D Neary; J S Snowden
Journal:  Parkinsonism Relat Disord       Date:  1996-04       Impact factor: 4.891

Review 5.  The representation of temporal information in perception and motor control.

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Journal:  Curr Opin Neurobiol       Date:  1996-12       Impact factor: 6.627

6.  Transgenic mice expressing a Huntington's disease mutation are resistant to quinolinic acid-induced striatal excitotoxicity.

Authors:  O Hansson; A Petersén; M Leist; P Nicotera; R F Castilho; P Brundin
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7.  Subcellular localization of wild-type and Parkinson's disease-associated mutant alpha -synuclein in human and transgenic mouse brain.

Authors:  P J Kahle; M Neumann; L Ozmen; V Muller; H Jacobsen; A Schindzielorz; M Okochi; U Leimer; H van Der Putten; A Probst; E Kremmer; H A Kretzschmar; C Haass
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8.  Absence of tissue plasminogen activator gene or activity impairs mouse cerebellar motor learning.

Authors:  Nicholas W Seeds; Mark E Basham; Jayne E Ferguson
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9.  6-OHDA induced effects upon the acquisition and performance of specific locomotor tasks in rats.

Authors:  M Watson; J G McElligott
Journal:  Pharmacol Biochem Behav       Date:  1983-06       Impact factor: 3.533

10.  The influence of external timing cues upon the rhythm of voluntary movements in Parkinson's disease.

Authors:  J S Freeman; F W Cody; W Schady
Journal:  J Neurol Neurosurg Psychiatry       Date:  1993-10       Impact factor: 10.154

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  6 in total

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2.  Learning new sequential stepping patterns requires striatal plasticity during the earliest phase of acquisition.

Authors:  Toru Nakamura; Masatoshi Nagata; Takeshi Yagi; Ann M Graybiel; Tetsuo Yamamori; Takashi Kitsukawa
Journal:  Eur J Neurosci       Date:  2017-02-27       Impact factor: 3.386

3.  Expression pattern of immediate early genes in the cerebellum of D1R KO, D2R KO, and wild type mice under vestibular-controlled activity.

Authors:  Toru Nakamura; Asako Sato; Takashi Kitsukawa; Toshikuni Sasaoka; Tetsuo Yamamori
Journal:  Front Cell Dev Biol       Date:  2015-06-17

4.  Pyramidal cell subtype-dependent cortical oscillatory activity regulates motor learning.

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Journal:  Commun Biol       Date:  2021-04-22

5.  Distinct motor impairments of dopamine D1 and D2 receptor knockout mice revealed by three types of motor behavior.

Authors:  Toru Nakamura; Asako Sato; Takashi Kitsukawa; Toshihiko Momiyama; Tetsuo Yamamori; Toshikuni Sasaoka
Journal:  Front Integr Neurosci       Date:  2014-07-15

6.  CalDAG-GEFI mediates striatal cholinergic modulation of dendritic excitability, synaptic plasticity and psychomotor behaviors.

Authors:  Jill R Crittenden; Shenyu Zhai; Magdalena Sauvage; Takashi Kitsukawa; Eric Burguière; Morgane Thomsen; Hui Zhang; Cinzia Costa; Giuseppina Martella; Veronica Ghiglieri; Barbara Picconi; Karen A Pescatore; Ellen M Unterwald; Walker S Jackson; David E Housman; S Barak Caine; David Sulzer; Paolo Calabresi; Anne C Smith; D James Surmeier; Ann M Graybiel
Journal:  Neurobiol Dis       Date:  2021-08-08       Impact factor: 5.996

  6 in total

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