The use of a plus-maze to measure anxiety in the mouse
- PMID: 3110839
- DOI: 10.1007/BF00177912
The use of a plus-maze to measure anxiety in the mouse
Abstract
To investigate whether an elevated plus-maze consisting of two open and two closed arms could be used as a model of anxiety in the mouse, NIH Swiss mice were tested in the apparatus immediately after a holeboard test. Factor analysis of data from undrugged animals tested in the holeboard and plus-maze yielded three orthogonal factors interpreted as assessing anxiety, directed exploration and locomotion. Anxiolytic drugs (chlordiazepoxide, sodium pentobarbital and ethanol) increased the proportion of time spent on the open arms, and anxiogenic drugs (FG 7142, caffeine and picrotoxin) reduced this measure. Amphetamine and imipramine failed to alter the indices of anxiety. The anxiolytic effect of chlordiazepoxide was reduced in mice that had previously experienced the plus-maze in an undrugged state. Testing animals in the holeboard immediately before the plus-maze test significantly elevated both the percentage of time spent on the open arms and the total number of arm entries, but did not affect the behavioral response to chlordiazepoxide. The plus-maze appears to be a useful test with which to investigate both anxiolytic and anxiogenic agents.
Similar articles
-
Validation of open:closed arm entries in an elevated plus-maze as a measure of anxiety in the rat.J Neurosci Methods. 1985 Aug;14(3):149-67. doi: 10.1016/0165-0270(85)90031-7. J Neurosci Methods. 1985. PMID: 2864480
-
Evidence that the anxiolytic-like effects of chlordiazepoxide on the elevated plus maze are confounded by increases in locomotor activity.Psychopharmacology (Berl). 1995 Apr;118(3):316-23. doi: 10.1007/BF02245961. Psychopharmacology (Berl). 1995. PMID: 7617825
-
Influence of spatial and temporal manipulations on the anxiolytic efficacy of chlordiazepoxide in mice previously exposed to the elevated plus-maze.Neurosci Biobehav Rev. 1999 Nov;23(7):971-80. doi: 10.1016/s0149-7634(99)00030-5. Neurosci Biobehav Rev. 1999. PMID: 10580311
-
Factors controlling measures of anxiety and responses to novelty in the mouse.Behav Brain Res. 2001 Nov 1;125(1-2):151-7. doi: 10.1016/s0166-4328(01)00292-3. Behav Brain Res. 2001. PMID: 11682106 Review.
-
Anxiogenic properties of beta-CCE and FG 7142: a review of promises and pitfalls.Psychopharmacology (Berl). 1988;94(4):452-63. doi: 10.1007/BF00212837. Psychopharmacology (Berl). 1988. PMID: 3131790 Review.
Cited by
-
Behavioural and functional characterization of Kv10.1 (Eag1) knockout mice.Hum Mol Genet. 2013 Jun 1;22(11):2247-62. doi: 10.1093/hmg/ddt076. Epub 2013 Feb 18. Hum Mol Genet. 2013. PMID: 23424202 Free PMC article.
-
Therapeutic potential of diosmin, a citrus flavonoid against arsenic-induced neurotoxicity via suppression of NOX 4 and its subunits.Indian J Pharmacol. 2021 Mar-Apr;53(2):132-142. doi: 10.4103/ijp.IJP_837_19. Indian J Pharmacol. 2021. PMID: 34100397 Free PMC article.
-
Mephedrone and nicotine: oxidative stress and behavioral interactions in animal models.Neurochem Res. 2015 May;40(5):1083-93. doi: 10.1007/s11064-015-1566-5. Epub 2015 Apr 11. Neurochem Res. 2015. PMID: 25862193 Free PMC article.
-
Diazepam causes sedative rather than anxiolytic effects in C57BL/6J mice.Sci Rep. 2021 Apr 29;11(1):9335. doi: 10.1038/s41598-021-88599-5. Sci Rep. 2021. PMID: 33927265 Free PMC article.
-
Neuropharmacological activities of Taxus wallichiana bark in Swiss albino mice.Indian J Pharmacol. 2015 May-Jun;47(3):299-303. doi: 10.4103/0253-7613.157128. Indian J Pharmacol. 2015. PMID: 26069368 Free PMC article.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical