Habituation, discrimination and anxiety in transgenic mice overexpressing acetylcholinesterase splice variants

Ora Kofman, Yehoshua Shavit, Sarit Ashkenazi, Shai Gabay

Research output: Contribution to journalArticlepeer-review

Abstract

TgS and TgR transgenic mice overexpress different splice variants of acetylcholinesterase and serve as models for genetic disruption of the cholinergic system. Whereas the TgS mouse overexpresses synaptic AChE, the TgR mouse overexpresses the rare readthrough variant whose C-terminal lacks the cysteine residue which permits adherence to the membrane. The two genotypes were compared to the parent strain, FVB/N mice on locomotion, discrimination learning and anxiety behavior following two exposures to the elevated plus maze. Male TgS mice were slower to acquire a simple odor discrimination, failed to habituate to a novel environment but were not impaired on reversal or set shifting compared to the FVB/N or TgR mice. In addition, TgS mice showed less avoidance behavior on the first exposure and but less exploration on the second exposure to the EPM. TgR mice were not impaired on discrimination learning; however, the females showed excessive running in circles in the activity meter. The findings suggest that the effects of overexpression of AChE are unique to different splice variants and may be sex-dependent.

Original languageEnglish
Pages (from-to)170-178
Number of pages9
JournalBrain Research
Volume1185
Issue number1
DOIs
StatePublished - 14 Dec 2007
Externally publishedYes

Bibliographical note

Funding Information:
The authors are grateful to Professor Hermona Soreq, Ph.D. from the Department of Biochemical Chemistry, and Yissum Research Development Company of the Hebrew University of Jerusalem for the transgenic mice that were developed in her lab. We also thank Mr. Liron Inbar for technical assistance. This research was funded by the Israel Science Foundation grant 856/01 to OK.

Keywords

  • Acetylcholinesterase
  • Discrimination learning
  • Elevated plus maze
  • Locomotor activity
  • Transgenic

ASJC Scopus subject areas

  • General Neuroscience
  • Molecular Biology
  • Clinical Neurology
  • Developmental Biology

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