Mice lacking the β4 subunit of the nicotinic acetylcholine receptor show memory deficits, altered anxiety- and depression-like behavior, and diminished nicotine-induced analgesia

Nicotine Tob Res. 2012 Nov;14(11):1346-55. doi: 10.1093/ntr/nts107. Epub 2012 May 9.

Abstract

Rationale: The role of β4-containing nicotinic acetylcholine receptors (nAChRs) in cognition, anxiety, depression, and analgesia in the absence of nicotine is unclear.

Methods: Wild-type (β4(+/+)) and knockout (β4(-/-)) mice for the nAChR β4 subunit were tested in behavioral tests assessing cognitive function, affective behaviors, and nociception.

Results: There were no learning and memory deficits in β4(-/-) mice compared with β4(+/+) mice during the acquisition of the Barnes maze, contextual fear conditioning, and Y maze tasks. In the Barnes maze memory retention test, male β4(-/-) mice showed reduced use of the spatial search strategy, indicating small spatial memory deficits compared with β4(+/+) mice. In the cue-induced fear conditioning memory retention test, β4(-/-) mice exhibited reduced freezing time compared with β4(+/+) mice. Compared with β4(+/+) mice, β4(-/-) mice exhibited decreased anxiety-like behavior in the light-dark box. Depression-like behavior in β4(-/-) mice was decreased in the tail suspension test and increased in the forced swim test compared with β4(+/+) mice. β4(-/-) mice did not differ from β4(+/+) mice in basal nociception but were less sensitive to the antinociceptive effect of nicotine in 2 tests of acute thermal pain.

Conclusions: Lack of β4-containing nAChRs resulted in small deficits in hippocampus- and amygdala-dependent memory retention functions. β4-containing nAChRs are involved in anxiety- and depression-like behaviors and contribute to the analgesic effects of nicotine.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Amygdala / physiology
  • Analgesics / pharmacology
  • Animals
  • Anxiety
  • Behavior, Animal
  • Cognition / physiology*
  • Conditioning, Psychological
  • Cues
  • Depression / genetics*
  • Fear
  • Female
  • Learning / physiology*
  • Male
  • Maze Learning
  • Memory Disorders / genetics*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Motor Activity
  • Nerve Tissue Proteins / genetics*
  • Nerve Tissue Proteins / metabolism
  • Nicotine / pharmacology
  • Receptors, Nicotinic / genetics*
  • Receptors, Nicotinic / metabolism

Substances

  • Analgesics
  • Chrnb4 protein, mouse
  • Nerve Tissue Proteins
  • Receptors, Nicotinic
  • Nicotine