4.5 Article

Motor function and dopamine release measurements in transgenic Huntington's disease model rats

Journal

BRAIN RESEARCH
Volume 1450, Issue -, Pages 148-156

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.brainres.2012.02.042

Keywords

Dopamine; Huntington's disease; Microelectrode; Voltammetry; Behavior; Transgenic

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Funding

  1. Hereditary Disease Foundation
  2. NIH of the National Center for Research Resources
  3. Lifespan Institute
  4. University of Kansas

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Huntington's disease (HD) is a fatal, genetic, neurodegenerative disorder characterized by deficits in motor and cognitive function. Here, we have quantitatively characterized motor deficiencies and dopamine release dynamics in transgenic HD model rats. Behavioral analyses were conducted using a newly-developed force-sensing runway and a previously-developed force-plate actometer. Gait disturbances were readily observed in transgenic HD rats at 12 to 15 months of age. Additionally, dopamine system challenge by ip injection of amphetamine also revealed that these rats were resistant to the expression of focused stereotypy compared to wild-type controls. Moreover, dopamine release, evoked by the application of single and multiple electrical stimulus pulses applied at different frequencies, and measured using fast-scan cyclic voltammetry at carbon-fiber microelectrodes, was diminished in transgenic HD rats compared to age-matched wild-type control rats. Collectively, these results underscore the potential contribution of dopamine release alterations to the expression of motor impairments in transgenic HD rats. (C) 2012 Elsevier B.V. All rights reserved.

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