Neurophysiological Assessment of Huntington's Disease Model Mice

Methods Mol Biol. 2018:1780:163-177. doi: 10.1007/978-1-4939-7825-0_9.

Abstract

Electrophysiological and cell imaging techniques are powerful tools for understanding alterations in neuronal activity in Huntington's disease (HD), a fatal neurological disorder caused by an expansion of CAG repeats in the HTT gene. Changes in neuronal activity often precede the behavioral manifestations of HD, therefore, understanding the electrophysiology of HD is critical for identifying potential prodromal markers and therapeutic targets. This chapter outlines the basic methodology behind four major electrophysiological and imaging techniques used in HD mouse models: patch clamp recordings, optogenetics, in vivo electrophysiology, and Ca2+ imaging, as well as some of the advancements in HD research using each of these techniques.

Keywords: Calcium imaging; Electrophysiology; In vivo recordings; Optogenetics; Patch clamp; Slice recordings.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Corpus Striatum / diagnostic imaging
  • Corpus Striatum / pathology
  • Corpus Striatum / physiopathology*
  • Disease Models, Animal
  • Electrodes
  • Electrophysiological Phenomena
  • Humans
  • Huntingtin Protein / genetics
  • Huntington Disease / genetics
  • Huntington Disease / pathology
  • Huntington Disease / physiopathology*
  • Mice
  • Mice, Transgenic
  • Optical Imaging / instrumentation
  • Optical Imaging / methods*
  • Optogenetics / instrumentation
  • Optogenetics / methods*
  • Patch-Clamp Techniques / instrumentation
  • Patch-Clamp Techniques / methods
  • Video Recording / instrumentation
  • Video Recording / methods*

Substances

  • Htt protein, mouse
  • Huntingtin Protein