Overexpression of α3/α5/β4 nicotinic receptor subunits modifies impulsive-like behavior

Drug Alcohol Depend. 2012 May 1;122(3):247-52. doi: 10.1016/j.drugalcdep.2011.09.027. Epub 2011 Oct 22.

Abstract

Recent studies have revealed that sequence variants in genes encoding the α3/α5/β4 nicotinic acetylcholine receptor subunits are associated with nicotine dependence. In this study, we evaluated two specific aspects of executive functioning related to drug addiction (impulsivity and working memory) in transgenic mice over expressing α3/α5/β4 nicotinic receptor subunits. Impulsivity and working memory were evaluated in an operant delayed alternation task, where mice must inhibit responding between 2 and 8s in order to receive food reinforcement. Working memory was also evaluated in a spontaneous alternation task in an open field. Transgenic mice showed less impulsive-like behavior than wild-type controls, and this behavioral phenotype was related to the number of copies of the transgene. Thus, transgenic Line 22 (16-28 copies) showed a more pronounced phenotype than Line 30 (4-5 copies). Overexpression of these subunits in Line 22 reduced spontaneous alternation behavior suggesting deficits in working memory processing in this particular paradigm. These results reveal the involvement of α3/α5/β4 nicotinic receptor subunits in working memory and impulsivity, two behavioral traits directly related to the vulnerability to develop nicotine dependence.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Gene Expression Regulation* / physiology
  • Humans
  • Impulsive Behavior / genetics*
  • Impulsive Behavior / metabolism*
  • Impulsive Behavior / prevention & control
  • Male
  • Memory, Short-Term / physiology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Motor Activity / genetics
  • Nerve Tissue Proteins / biosynthesis*
  • Nerve Tissue Proteins / genetics
  • Neural Inhibition / genetics
  • Protein Subunits / biosynthesis*
  • Protein Subunits / genetics*
  • Protein Subunits / physiology
  • Random Allocation
  • Receptors, Nicotinic / biosynthesis*
  • Receptors, Nicotinic / genetics

Substances

  • Chrnb4 protein, mouse
  • Nerve Tissue Proteins
  • Protein Subunits
  • Receptors, Nicotinic
  • nicotinic receptor alpha5 subunit, mouse
  • nicotinic receptor subunit alpha3