Visual response properties in the dorsal lateral geniculate nucleus of mice lacking the beta2 subunit of the nicotinic acetylcholine receptor

J Neurosci. 2004 Sep 29;24(39):8459-69. doi: 10.1523/JNEUROSCI.1527-04.2004.

Abstract

We present a quantitative description of single-cell visual response properties in the dorsal lateral geniculate nucleus (dLGN) of anesthetized adult mice lacking the beta2 subunit of the nicotinic acetylcholine receptor (beta2-/-) and compare these response properties with data from wild-type animals. Some response features, including all spatial receptive field characteristics and bursting behavior, are entirely normal in beta2-/- dLGN cells. In other respects, the responses of beta2-/- dLGN cells are quantitatively abnormal: the mutation is associated with higher spontaneous and visually evoked firing rates, faster visual response latencies, a preference for higher temporal frequencies, and a trend toward greater contrast sensitivity. The normal response properties in the beta2-/- dLGN show that none of the many effects of the mutation, including disrupted geniculate functional organization and abnormal cholinergic transmission, have any effect on spatial response characteristics and bursting behavior in dLGN neurons. The abnormal response characteristics in the beta2-/- dLGN are most interesting in that they are no worse than normal; any visual processing deficits found in studies of the beta2-/- visual cortex must therefore arise solely from abnormalities in cortical processing.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / physiology
  • Animals
  • Contrast Sensitivity / physiology
  • Female
  • Geniculate Bodies / cytology
  • Geniculate Bodies / physiology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Models, Neurological
  • Neurons / physiology
  • Photic Stimulation / methods
  • Receptors, Nicotinic / genetics
  • Receptors, Nicotinic / physiology*
  • Sex Factors
  • Space Perception / physiology
  • Time Factors
  • Visual Pathways / cytology
  • Visual Pathways / physiology*

Substances

  • Receptors, Nicotinic
  • nicotinic receptor beta2