4.4 Article

The response of neuregulin 1 mutant mice to acute restraint stress

Journal

NEUROSCIENCE LETTERS
Volume 515, Issue 1, Pages 82-86

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.neulet.2012.03.024

Keywords

Neuregulin 1; Animal model; Schizophrenia; Restraint stress; Locomotion; Corticosterone

Categories

Funding

  1. Schizophrenia Research Institute
  2. NSW Ministry of Health
  3. National Health and Medical Research Council of Australia (NHMRC) [568752, 1003886]
  4. National Alliance for Research on Schizophrenia and Depression
  5. NHMRC [481355]

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Stress plays a role in the development and severity of psychotic symptoms and there may be a genetic component to stress vulnerability in schizophrenia. Using an established mouse model for schizophrenia, we investigated the behavioural and endocrine response of Nrg1 transmembrane domain mutant mice (Nrg1 HET) and wild type-like (WT) littermates to acute restraint stress. Animals were screened at 3-4 months and 6-7 months of age (before and after onset of hyperlocomotion) for open field behaviour and serum corticosterone levels. In younger mice, stress reduced locomotive and explorative measures and increased anxiety-like behaviour regardless of genotype. Older Nrg1 mutants were less susceptible to the effects of stress on anxiety-related behaviours. All mice responded to restraint stress with robust increases in serum corticosterone. Importantly, the stress-induced increase in corticosterone was more pronounced in Nrg1 mutant than WT mice at the younger but not the older age. Our results suggest that transmembrane domain Nrg1 has only a moderate effect on the acute stress response of mice. The behavioural differences detected between WT and Nrg1 HET mice at the older age were evident without parallel modifications to the glucocorticoid system. (C) 2012 Elsevier Ireland Ltd. All rights reserved.

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