Skip to main content
Log in

Anxiety in the Elevated Zero-Maze Is Augmented in Mice After Repeated Daily Exposure

  • Published:
Behavior Genetics Aims and scope Submit manuscript

Abstract

We recently tested three inbred mouse strains (C57BL/6J, DBA/2J, C3H/HeJ) and two F1 hybrids (B6C3F1/J, C3D2F1/J) in an elevated zero-maze for 3 consecutive days. As measured by the latency to enter an open quadrant and percentage of time spent in the open, anxiety increased over the three trials. Furthermore, we observed that some strains used visual cues to avoid the open arms of the zero-maze on the initial exposure, while other strains may have used other sensory cues. These results suggest that strains differentially use or retain information, gathered from the initial exposure, to avoid the open quadrants on subsequent exposure to the maze. Moreover, this repeated trial test may more accurately reflect anxiety in strains that are visually impaired.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

REFERENCES

  • Almeida, S. S., Garcia, R. A., and de Oliveira, L. M. (1993). Effects of protein malnutrition and repeated testing upon locomotor and exploratory behaviors in the elevated plus-maze. Phys. Behav. 54:749–752.

    Google Scholar 

  • Bickerdike, M. J., Marsden, C. A., Dourish, C. T., and Fletcher, A. (1994). The influence of 5-hydroxytryptamine re-uptake blockade on CCK receptor antagonist effects in the rat elevated zeromaze. Eur. J. Pharm. 271:403–411.

    Google Scholar 

  • Bolivar, V. J., Caldarone, B. J., Reilly, A. A., and Flaherty, L. (2000). Habituation of activity in an open field: A survey of inbred strains and F1 hybrids. Behav. Genet. 30:285–293.

    Google Scholar 

  • Cook, M. N., Williams, R. W., and Flaherty, L. (2001). Anxietyrelated behaviors in the elevated zero-maze are affected by genetic factors and retinal degeneration. Behav. Neurosci. 115:468–476.

    Google Scholar 

  • Espejo, E. F. (1997). Effects of weekly or daily exposure to the elevated plus-maze in male mice. Behav. Br. Res. 87:233–238.

    Google Scholar 

  • Fernandes, C., and File, S. E. (1996). The influence of open arm ledges and maze experience in the elevated plus-maze. Pharmacol. Biochem. Behav. 54:31–40.

    Google Scholar 

  • Hogg, S. (1996). A review of the validity and variability of the elevated plus-maze as an animal model of anxiety. Pharm. Biochem. Behav. 54:21–30.

    Google Scholar 

  • Holmes, A., and Rodgers, R. J. (1998). Responses of swiss-webster mice to repeated plus-maze experience: further evidence for a qualitative shift in emotional state? Pharm. Biochem. Behav. 60: 473–488.

    Google Scholar 

  • Menard, J., and Treit, D. (1999). Effects of centrally administered anxiolytic compounds on animal models of anxiety. Neurosci. Biobehav. Revs. 23:591–613.

    Google Scholar 

  • Owen, E. H., Logue, S. F., Rasmussen, D. L., and Wehner, J. M. (1997). Assessment of learning by the Morris water task and fear conditioning in inbred mouse strains and F1 hybrids: Implications of genetic background for single gene mutations and quantitative trait loci analyses. Neuroscience 80:1087–1099.

    Google Scholar 

  • Pellow, S., and File, S. E. (1986). Anxiolytic and anxiogenic drug effects on exploratory activity in an elevated plus-maze: A novel test of anxiety in the rat. J. Neurosci. Meth. 24:525–529.

    Google Scholar 

  • Rodgers, R. J., Johnson, N. J. T., Cole, J. C., Dewar, C. V., Kidd, G. R., and Kimpson, P. H. (1996). Plus-maze retest profile in mice: Importance of initial stages of trial 1 and response to post-trial cholinergic receptor blockade. Pharm. Biochem. Behav. 54:41–50.

    Google Scholar 

  • Rodgers, R. J., and Shepherd, J. K. (1993). Influence of prior maze experience on behaviour and response of diazepam in the elevated plus maze and light/dark tests. Psychopharmacology 113:237–242.

    Google Scholar 

  • Shepherd, J. K., Grewal., S. S., Fletcher, A., Bill, D. J., and Dourish, C. T. (1994). Behavioral and pharmacological characterisation of the elevated “zero-maze” as an animal model of anxiety. Psychopharmacology 116:56–64.

    Google Scholar 

  • Treit, D., Menard, J., and Royan, C. (1993). Anxiogenic stimuli in the elevated plus maze. Pharm. Biochem. Behav. 44:463–469.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Lorraine Flaherty.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Cook, M.N., Crounse, M. & Flaherty, L. Anxiety in the Elevated Zero-Maze Is Augmented in Mice After Repeated Daily Exposure. Behav Genet 32, 113–118 (2002). https://doi.org/10.1023/A:1015249706579

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1015249706579

Navigation