4.6 Article

Wfs1-deficient mice display impaired behavioural adaptation in stressful environment

Journal

BEHAVIOURAL BRAIN RESEARCH
Volume 198, Issue 2, Pages 334-345

Publisher

ELSEVIER
DOI: 10.1016/j.bbr.2008.11.007

Keywords

WfS1; Wolfram syndrome; Transgenic mice; Homologous recombination; Stress; Corticosterone; Anxiety; Behavioural adaptation; Stress-induced analgesia; Motility box; Amphetamine; Apomorphine; Mesolimbic system; Dopamine; Exploratory behaviour; Diazepam; Rota-rod; Hyponeophagia; Fear conditioning; Morris water maze; Active avoidance; Forced swimming test; Elevated plus-maze test; Light-dark exploration test

Funding

  1. Estonian Science Foundation [6590, 7651]
  2. Ministry of Science and Education [SF0180125s08]
  3. European Regional Development Fund

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Wfs1-deficient mice were generated by disrupting the 8th exon of Wfs1 gene. Reproduction rates of homozygous Wfs1-deficient mice were slightly below the expected values, they displayed intolerance to glucose and overall lower body weight. The present behavioural study was performed in female Wfs1deficient mice due to their milder metabolic disturbances. Non-fasting blood glucose levels did not differ between homozygous Wfs1-deficient mice and wild-type littermates. While there was no difference in baseline plasma corticosterone, exposure to stress induced a nearly three-fold elevation of corticosterone in Wfs1-deficient mice in relation to wild-type littermates. Wfs1-deficient mice did not display obvious shortcomings in sensory and motor functioning as exemplified by intact responses in conditioned learning paradigms and rota-rod test. Locomotor activity of Wfs1-deficient mice was significantly lower only in brightly lit environment. Short-term isolation had a significant anxiogenic-like effect on the behaviour of Wfs1-deficient mice in dark/light exploration test. Lower exploratory activity of Wfs1-deficient mice in the plus-maze was antagonised by pre-treatment with diazepam (1 mg/kg), a GABA(A) receptor agonist. Wfs1-deficient mice displayed increased anxiety-like behaviour in hyponeophagia test. The locomotor stimulatory effects of amphetamine (2.5-7.5 mg/kg) and apomorphine (3 mg/kg) were significantly attenuated and facilitated, respectively, in Wfs1-deficient mice. There were no differences between Wfs1-deficient mice and wild-types in forced swimming behaviour and conditioned fear responses. Subtle impairments in reversal learning were apparent in Wfs1-deficient mice in the Morris water maze. Altogether, the present study demonstrates impaired behavioural adaptation of Wfs1-deficient mice in stress-inducing situations. It is likely that Wfs1 protein plays a major role in the behavioural adaptation mechanisms to novel and stressful environments. (C) 2008 Elsevier B.V. All rights reserved.

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