Literature DB >> 9300621

Effects of diazepam and buspirone on the behaviour of wild voles (Microtus socialis) in two models of anxiety.

C A Hendrie1, D Eilam, S M Weiss.   

Abstract

Exploration models of anxiety rely almost universally on the use of laboratory species. Furthermore, the spontaneous patterns of locomotion displayed are often interpreted as being an expression of antipredator defense. However, there is no direct link between the experience of these animals and the proposed motivation for their behaviour. To address this problem, the behaviour of wild trapped voles (Microtus socialis), a small-rodent species that is heavily predated upon, was examined in the elevated plus-maze and the black/white exploration model. It was hypothesised that the patterns of locomotion in these exploration models of anxiety should be similar to those reported for laboratory animals if the reactions of the laboratory animals are related to antipredator defense. Data revealed that voles show a similar preference for the protected areas in these models (closed arms or dark section) and that this preference can be modified by buspirone and diazepam. Interestingly, although the effective doses of each drug was the same within each model, it differed between models, with the minimum effective doses of these compounds being lower in the black/white exploration model (1 mg/kg) than in the elevated plus-maze (4 mg/kg). These data provide valuable information concerning the actions of anxiolytic compounds in wild trapped animals as assessed by formal laboratory models and provide useful verification that findings in these models may be generalised to species other than laboratory rodents.

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Year:  1997        PMID: 9300621     DOI: 10.1016/s0091-3057(97)00278-5

Source DB:  PubMed          Journal:  Pharmacol Biochem Behav        ISSN: 0091-3057            Impact factor:   3.533


  8 in total

1.  Abandoned prairie vole mothers show normal maternal care but altered emotionality: Potential influence of the brain corticotropin-releasing factor system.

Authors:  Oliver J Bosch; Tobias T Pohl; Inga D Neumann; Larry J Young
Journal:  Behav Brain Res       Date:  2017-12-27       Impact factor: 3.332

2.  The use of the elevated plus maze as an assay of anxiety-related behavior in rodents.

Authors:  Alicia A Walf; Cheryl A Frye
Journal:  Nat Protoc       Date:  2007       Impact factor: 13.491

3.  The CRF system mediates increased passive stress-coping behavior following the loss of a bonded partner in a monogamous rodent.

Authors:  Oliver J Bosch; Hemanth P Nair; Todd H Ahern; Inga D Neumann; Larry J Young
Journal:  Neuropsychopharmacology       Date:  2008-10-15       Impact factor: 7.853

4.  Local oxytocin tempers anxiety by activating GABAA receptors in the hypothalamic paraventricular nucleus.

Authors:  Adam S Smith; Manal Tabbaa; Kelly Lei; Patrick Eastham; Michael J Butler; Latanya Linton; Randy Altshuler; Yan Liu; Zuoxin Wang
Journal:  Psychoneuroendocrinology       Date:  2015-09-21       Impact factor: 4.905

5.  The olfactory hole-board test in rats: a new paradigm to study aversion and preferences to odors.

Authors:  Kerstin E A Wernecke; Markus Fendt
Journal:  Front Behav Neurosci       Date:  2015-08-25       Impact factor: 3.558

6.  An elevated plus-maze in mixed reality for studying human anxiety-related behavior.

Authors:  Sarah V Biedermann; Daniel G Biedermann; Frederike Wenzlaff; Tim Kurjak; Sawis Nouri; Matthias K Auer; Klaus Wiedemann; Peer Briken; Jan Haaker; Tina B Lonsdorf; Johannes Fuss
Journal:  BMC Biol       Date:  2017-12-21       Impact factor: 7.431

Review 7.  Preclinical animal anxiety research - flaws and prejudices.

Authors:  Abdelkader Ennaceur; Paul L Chazot
Journal:  Pharmacol Res Perspect       Date:  2016-03-08

8.  Behavioral Effects of Buspirone in Juvenile Zebrafish of Two Different Genetic Backgrounds.

Authors:  Amira Abozaid; Robert Gerlai
Journal:  Toxics       Date:  2022-01-07
  8 in total

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