Post-weaning social isolation of rats leads to long-term disruption of the gut microbiota-immune-brain axis
Early-life stress is an established risk for the development of psychiatric disorders. Post-weaning isolation rearing of rats produces lasting developmental changes in behavior and brain function that may have translational pathophysiological relevance to alterations seen in schizophrenia, but the u...
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| Format: | Article |
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Elsevier
2017
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| Online Access: | https://eprints.nottingham.ac.uk/47823/ |
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| author | Doherty, Fionn Dunphy O’Mahony, Siobhain M. Peterson, Veronica L. O’Sullivan, Orla Crispie, Fiona Cotter, Paul D. Wigmore, Peter King, Madeleine V. Cryan, John F. Fone, Kevin C.F. |
| author_facet | Doherty, Fionn Dunphy O’Mahony, Siobhain M. Peterson, Veronica L. O’Sullivan, Orla Crispie, Fiona Cotter, Paul D. Wigmore, Peter King, Madeleine V. Cryan, John F. Fone, Kevin C.F. |
| author_sort | Doherty, Fionn Dunphy |
| building | Nottingham Research Data Repository |
| collection | Online Access |
| description | Early-life stress is an established risk for the development of psychiatric disorders. Post-weaning isolation rearing of rats produces lasting developmental changes in behavior and brain function that may have translational pathophysiological relevance to alterations seen in schizophrenia, but the underlying mechanisms are unclear. Accumulating evidence supports the premise that gut microbiota influence brain development and function by affecting inflammatory mediators, the hypothalamic-pituitary-adrenal axis and neurotransmission, but there is little knowledge of whether the microbiota-gut-brain axis might contribute to the development of schizophrenia-related behaviors. To this end the effects of social isolation (SI; a well-validated animal model for schizophrenia)-induced changes in rat behavior were correlated with alterations in gut microbiota, hippocampal neurogenesis and brain cytokine levels. Twenty-four male Lister hooded rats were housed in social groups (group-housed, GH, 3 littermates per cage) or alone (SI) from weaning (post-natal day 24) for four weeks before recording open field exploration, locomotor activity/novel object discrimination (NOD), elevated plus maze, conditioned freezing response (CFR) and restraint stress at one week intervals. Post-mortem caecal microbiota composition, cortical and hippocampal cytokines and neurogenesis were correlated to indices of behavioral changes. SI rats were hyperactive in the open field and locomotor activity chambers traveling further than GH controls in the less aversive peripheral zone. While SI rats showed few alterations in plus maze or NOD they froze for significantly less time than GH following conditioning in the CFR paradigm, consistent with impaired associative learning and memory. SI rats had significantly fewer BrdU/NeuN positive cells in the dentate gyrus than GH controls. SI rats had altered microbiota composition with increases in Actinobacteria and decreases in the class Clostridia compared to GH controls. Differences were also noted at genus level. Positive correlations were seen between microbiota, hippocampal IL-6 and IL-10, conditioned freezing and open field exploration. Adverse early-life stress resulting from continuous SI increased several indices of ‘anxiety-like’ behavior and impaired associative learning and memory accompanied by changes to gut microbiota, reduced hippocampal IL-6, IL-10 and neurogenesis. This study suggests that early-life stress may produce long-lasting changes in gut microbiota contributing to development of abnormal neuronal and endocrine function and behavior which could play a pivotal role in the aetiology of psychiatric illness. |
| first_indexed | 2025-11-14T20:07:03Z |
| format | Article |
| id | nottingham-47823 |
| institution | University of Nottingham Malaysia Campus |
| institution_category | Local University |
| last_indexed | 2025-11-14T20:07:03Z |
| publishDate | 2017 |
| publisher | Elsevier |
| recordtype | eprints |
| repository_type | Digital Repository |
| spelling | nottingham-478232020-05-04T19:15:15Z https://eprints.nottingham.ac.uk/47823/ Post-weaning social isolation of rats leads to long-term disruption of the gut microbiota-immune-brain axis Doherty, Fionn Dunphy O’Mahony, Siobhain M. Peterson, Veronica L. O’Sullivan, Orla Crispie, Fiona Cotter, Paul D. Wigmore, Peter King, Madeleine V. Cryan, John F. Fone, Kevin C.F. Early-life stress is an established risk for the development of psychiatric disorders. Post-weaning isolation rearing of rats produces lasting developmental changes in behavior and brain function that may have translational pathophysiological relevance to alterations seen in schizophrenia, but the underlying mechanisms are unclear. Accumulating evidence supports the premise that gut microbiota influence brain development and function by affecting inflammatory mediators, the hypothalamic-pituitary-adrenal axis and neurotransmission, but there is little knowledge of whether the microbiota-gut-brain axis might contribute to the development of schizophrenia-related behaviors. To this end the effects of social isolation (SI; a well-validated animal model for schizophrenia)-induced changes in rat behavior were correlated with alterations in gut microbiota, hippocampal neurogenesis and brain cytokine levels. Twenty-four male Lister hooded rats were housed in social groups (group-housed, GH, 3 littermates per cage) or alone (SI) from weaning (post-natal day 24) for four weeks before recording open field exploration, locomotor activity/novel object discrimination (NOD), elevated plus maze, conditioned freezing response (CFR) and restraint stress at one week intervals. Post-mortem caecal microbiota composition, cortical and hippocampal cytokines and neurogenesis were correlated to indices of behavioral changes. SI rats were hyperactive in the open field and locomotor activity chambers traveling further than GH controls in the less aversive peripheral zone. While SI rats showed few alterations in plus maze or NOD they froze for significantly less time than GH following conditioning in the CFR paradigm, consistent with impaired associative learning and memory. SI rats had significantly fewer BrdU/NeuN positive cells in the dentate gyrus than GH controls. SI rats had altered microbiota composition with increases in Actinobacteria and decreases in the class Clostridia compared to GH controls. Differences were also noted at genus level. Positive correlations were seen between microbiota, hippocampal IL-6 and IL-10, conditioned freezing and open field exploration. Adverse early-life stress resulting from continuous SI increased several indices of ‘anxiety-like’ behavior and impaired associative learning and memory accompanied by changes to gut microbiota, reduced hippocampal IL-6, IL-10 and neurogenesis. This study suggests that early-life stress may produce long-lasting changes in gut microbiota contributing to development of abnormal neuronal and endocrine function and behavior which could play a pivotal role in the aetiology of psychiatric illness. Elsevier 2017-11-02 Article PeerReviewed Doherty, Fionn Dunphy, O’Mahony, Siobhain M., Peterson, Veronica L., O’Sullivan, Orla, Crispie, Fiona, Cotter, Paul D., Wigmore, Peter, King, Madeleine V., Cryan, John F. and Fone, Kevin C.F. (2017) Post-weaning social isolation of rats leads to long-term disruption of the gut microbiota-immune-brain axis. Brain, Behavior, and Immunity, 68 . pp. 261-273. ISSN 0889-1591 isolation rearing microbiota cytokines anxiety learning and memory schizophrenia neurogenesis http://www.sciencedirect.com/science/article/pii/S0889159117304804 doi:10.1016/j.bbi.2017.10.024 doi:10.1016/j.bbi.2017.10.024 |
| spellingShingle | isolation rearing microbiota cytokines anxiety learning and memory schizophrenia neurogenesis Doherty, Fionn Dunphy O’Mahony, Siobhain M. Peterson, Veronica L. O’Sullivan, Orla Crispie, Fiona Cotter, Paul D. Wigmore, Peter King, Madeleine V. Cryan, John F. Fone, Kevin C.F. Post-weaning social isolation of rats leads to long-term disruption of the gut microbiota-immune-brain axis |
| title | Post-weaning social isolation of rats leads to long-term disruption of the gut microbiota-immune-brain axis |
| title_full | Post-weaning social isolation of rats leads to long-term disruption of the gut microbiota-immune-brain axis |
| title_fullStr | Post-weaning social isolation of rats leads to long-term disruption of the gut microbiota-immune-brain axis |
| title_full_unstemmed | Post-weaning social isolation of rats leads to long-term disruption of the gut microbiota-immune-brain axis |
| title_short | Post-weaning social isolation of rats leads to long-term disruption of the gut microbiota-immune-brain axis |
| title_sort | post-weaning social isolation of rats leads to long-term disruption of the gut microbiota-immune-brain axis |
| topic | isolation rearing microbiota cytokines anxiety learning and memory schizophrenia neurogenesis |
| url | https://eprints.nottingham.ac.uk/47823/ https://eprints.nottingham.ac.uk/47823/ https://eprints.nottingham.ac.uk/47823/ |