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Do housing-induced changes in brain activity cause stereotypic behaviours in laboratory mice?
Kitchenham, Lindsey; MacLellan, Aileen; Paletta, Pietro; Patel, Ashutosh; Choleris, Elena; Mason, Georgia.
Afiliación
  • Kitchenham L; Campbell Centre for the Study of Animal Welfare/Dept. of Integrative Biology, University of Guelph, Ontario, Canada.
  • MacLellan A; Campbell Centre for the Study of Animal Welfare/Dept. of Integrative Biology, University of Guelph, Ontario, Canada; Canadian Council on Animal Care; Ottawa Hospital Research Institute; University of Ottawa, Dept. of Anesthesiology and Pain Medicine.
  • Paletta P; Dept. of Psychology, Neuroscience and Applied Cognitive Sciences, University of Guelph, Ontario, Canada.
  • Patel A; Dept. of Biomedical Sciences, University of Guelph, Ontario, Canada.
  • Choleris E; Dept. of Psychology, Neuroscience and Applied Cognitive Sciences, University of Guelph, Ontario, Canada.
  • Mason G; Campbell Centre for the Study of Animal Welfare/Dept. of Integrative Biology, University of Guelph, Ontario, Canada. Electronic address: gmason@uoguelph.ca.
Behav Brain Res ; 462: 114862, 2024 Mar 28.
Article en En | MEDLINE | ID: mdl-38216059
ABSTRACT
Abnormal repetitive stereotypic behaviours (SBs) (e.g. pacing, body-rocking) are common in animals with poor welfare (e.g. socially isolated/in barren housing). But how (or even whether) poor housing alters animals' brains to induce SBs remains uncertain. To date, there is little evidence for environmental effects on the brain that also correlate with individual SB performance. Using female mice from two strains (SB-prone DBA/2s; SB-resistant C57/BL/6s), displaying two forms of SB (route-tracing; bar-mouthing), we investigated how housing (conventional laboratory conditions vs. well-resourced 'enriched' cages) affects long-term neuronal activity as assessed via cytochrome oxidase histochemistry in 13 regions of interest (across cortex, striatum, basal ganglia and thalamus). Conventional housing reduced activity in the cortex and striatum. However, DBA mice had no cortical or striatal differences from C57 mice (just greater basal ganglia output activity, independent of housing). Neural correlates for individual levels of bar-mouthing (positive correlations in the substantia nigra and thalamus) were also independent of housing; while route-tracing levels had no clear neural correlates at all. Thus conventional laboratory housing can suppress cortico-striatal activity, but such changes are unrelated to SB (since not mirrored by congruent individual and strain differences). Furthermore, the neural correlates of SB at individual and strain levels seem to reflect underlying predispositions, not housing-mediated changes. To aid further work, hypothesis-generating model fit analyses highlighted this unexplained housing effect, and also suggested several regions of interest across cortex, striatum, thalamus and substantia nigra for future investigation (ideally with improved power to reduce risks of Type II error).
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Conducta Estereotipada / Ganglios Basales Límite: Animals Idioma: En Revista: Behav Brain Res Año: 2024 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Conducta Estereotipada / Ganglios Basales Límite: Animals Idioma: En Revista: Behav Brain Res Año: 2024 Tipo del documento: Article País de afiliación: Canadá