Nicotine withdrawal-induced deficits in trace fear conditioning in C57BL/6 mice - A role for high-affinity β2 subunit-containing nicotinic acetylcholine receptors

J. D. Raybuck, T. J. Gould

Research output: Contribution to journalArticlepeer-review

46 Scopus citations

Abstract

Nicotine alters cognitive processes that include working memory and long-term memory. Trace fear conditioning may involve working memory during acquisition while also allowing the assessment of long-term memory. The present study used trace fear conditioning in C57BL/6 mice to investigate the effects of acute nicotine, chronic nicotine and withdrawal of chronic nicotine on processes active during acquisition and recall 24 h later and to examine the nicotinic acetylcholine receptor subtypes (nAChRs) involved in withdrawal deficits in trace fear conditioning. During training, acute nicotine (0.09 mg/kg) enhanced, but chronic nicotine (6.3 mg/kg/day, 13 days) and withdrawal of chronic nicotine (6.3 mg/kg/day, 12 days) had no significant effect on, acquisition of trace conditioning. At recall, acute treatment enhanced conditioning while chronic nicotine had no effect and withdrawal of chronic nicotine resulted in deficits. Antagonist-precipitated withdrawal was used to characterize the nAChRs involved in the withdrawal deficits. The low-affinity nAChR antagonist MLA (1.5, 3 or 9 mg/kg) had no effect on trace fear conditioning, but the high-affinity nAChR antagonist DHβE (3 mg/kg) precipitated deficits in trace fear conditioning if administered at training or training and testing, but not if administered at testing alone. The β2 nAChR subunit is involved in the withdrawal effects as withdrawal of chronic nicotine produced deficits in trace fear conditioning in wildtype but not in β2-knockout mice. Thus, nicotine alters processes involved in both acquisition and long-term memory of trace fear conditioning, and high-affinity β2 subunit-containing nAChRs are critically involved in the effects of nicotine withdrawal on trace fear conditioning.

Original languageEnglish (US)
Pages (from-to)377-387
Number of pages11
JournalEuropean Journal of Neuroscience
Volume29
Issue number2
DOIs
StatePublished - Jan 2009

Keywords

  • Addiction
  • Cognition
  • Hippocampus
  • Learning
  • Working memory

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