Basal activity level in mice predicts the initial and sensitized locomotor response to nicotine only in high responders

Behav Brain Res. 2014 May 1:264:143-50. doi: 10.1016/j.bbr.2014.01.046. Epub 2014 Feb 5.

Abstract

Not all humans become addicted to drugs of abuse following casual use. Thus, it is important to identify factors that may contribute to subsequent drug responding. Previous studies have identified characteristics such as novelty-seeking, impulsivity, and anxiety as factors involved in the progression to drug dependence. The current experiment investigated basal locomotor activity in C57Bl/6N mice as a potential predictor of subsequent nicotine responses. We examined the ability of differences in basal locomotor activity to predict the acute and sensitized response to nicotine, as well as nicotine conditioned reinforcement. A median split was used to distinguish between low and high responders with regard to basal locomotor activity in mice. We then measured the acute response to nicotine (0.5mg/kg IP) in these mice, followed by measures of conditioned place preference (CPP; 0.5mg/kg IP) and locomotor sensitization (0.5mg/kg IP), to determine whether basal locomotion is predictive of subsequent responding to nicotine. High, but not low, basal activity was found to be a predictor of both the acute and sensitized response to nicotine. Interestingly, only mice classified as having low basal activity demonstrated a significant CPP, suggesting that pre-exposure to nicotine differentially affects conditioned reinforcement on the basis of initial activity level. Basal locomotor activity may be an efficient measure of subsequent locomotor responding to nicotine, but only in animals classified as having high basal activity. However, animals with low basal locomotor activity may be more susceptible to the reinforcing properties of nicotine.

Keywords: Conditioned place preference; Locomotor activity; Locomotor sensitization; Nicotine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Conditioning, Operant / drug effects*
  • Dose-Response Relationship, Drug
  • Injections, Intraperitoneal
  • Locomotion / drug effects*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Nicotine / pharmacology*
  • Nicotinic Agonists / pharmacology*

Substances

  • Nicotinic Agonists
  • Nicotine