Proinflammatory cytokines differentially influence adult hippocampal cell proliferation depending upon the route and chronicity of administration
Julie Anne Seguin, Jordan Brennan, Emily Mangano, Shawn HayleyInstitute of Neuroscience, Carleton University, Ottawa, Ontario, CanadaAbstract: Disturbances of hippocampal plasticity, including impaired dendritic branching and reductions of neurogenesis, are provoked by stressful insults and may occu...
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Dove Medical Press
2008
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oai:doaj.org-article:8031b6a09f6945babf33fe4350530e152021-12-02T08:18:58ZProinflammatory cytokines differentially influence adult hippocampal cell proliferation depending upon the route and chronicity of administration1176-63281178-2021https://doaj.org/article/8031b6a09f6945babf33fe4350530e152008-12-01T00:00:00Zhttp://www.dovepress.com/proinflammatory-cytokines-differentially-influence-adult-hippocampal-c-a2656https://doaj.org/toc/1176-6328https://doaj.org/toc/1178-2021Julie Anne Seguin, Jordan Brennan, Emily Mangano, Shawn HayleyInstitute of Neuroscience, Carleton University, Ottawa, Ontario, CanadaAbstract: Disturbances of hippocampal plasticity, including impaired dendritic branching and reductions of neurogenesis, are provoked by stressful insults and may occur in depression. Although corticoids likely contribute to stressor-induced reductions of neurogenesis, other signaling messengers, including pro-inflammatory cytokines might also be involved. Accordingly, the present investigation assessed whether three proinflammatory cytokines, namely interleukin-1β (IL-1β), IL-6, and tumor necrosis factor-α (TNF-α) (associated with depression) influenced cellular proliferation within the hippocampus. In this regard, systemic administration of TNF-α reduced 5-bromo-2-deoxyuridine (BrdU) labeling within the hippocampus, whereas IL-1β and IL-6 had no such effect. However, repeated but not a single intra-hippocampal infusion of IL-6 and IL-1β actually increased cellular proliferation and IL-6 infusion also enhanced microglial staining within the hippocampus. Yet, no changes in doublecortin expression were apparent, suggesting that the cytokine did not influence the birth of cells destined to become neurons. Essentially, the route of administration and chronicity of cytokine administration had a marked influence upon the nature of hippocampal alterations provoked, suggesting that cytokines may differentially regulate hippocampal plasticity in neuropsychiatric conditions.Keywords: cytokine, depression, neuroplasticity, hippocampus, stressor Julie Anne SeguinJordan BrennanEmily ManganoShawn HayleyDove Medical PressarticleNeurosciences. Biological psychiatry. NeuropsychiatryRC321-571Neurology. Diseases of the nervous systemRC346-429ENNeuropsychiatric Disease and Treatment, Vol 2009, Iss default, Pp 5-14 (2008) |
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Neurosciences. Biological psychiatry. Neuropsychiatry RC321-571 Neurology. Diseases of the nervous system RC346-429 |
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Neurosciences. Biological psychiatry. Neuropsychiatry RC321-571 Neurology. Diseases of the nervous system RC346-429 Julie Anne Seguin Jordan Brennan Emily Mangano Shawn Hayley Proinflammatory cytokines differentially influence adult hippocampal cell proliferation depending upon the route and chronicity of administration |
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Julie Anne Seguin, Jordan Brennan, Emily Mangano, Shawn HayleyInstitute of Neuroscience, Carleton University, Ottawa, Ontario, CanadaAbstract: Disturbances of hippocampal plasticity, including impaired dendritic branching and reductions of neurogenesis, are provoked by stressful insults and may occur in depression. Although corticoids likely contribute to stressor-induced reductions of neurogenesis, other signaling messengers, including pro-inflammatory cytokines might also be involved. Accordingly, the present investigation assessed whether three proinflammatory cytokines, namely interleukin-1β (IL-1β), IL-6, and tumor necrosis factor-α (TNF-α) (associated with depression) influenced cellular proliferation within the hippocampus. In this regard, systemic administration of TNF-α reduced 5-bromo-2-deoxyuridine (BrdU) labeling within the hippocampus, whereas IL-1β and IL-6 had no such effect. However, repeated but not a single intra-hippocampal infusion of IL-6 and IL-1β actually increased cellular proliferation and IL-6 infusion also enhanced microglial staining within the hippocampus. Yet, no changes in doublecortin expression were apparent, suggesting that the cytokine did not influence the birth of cells destined to become neurons. Essentially, the route of administration and chronicity of cytokine administration had a marked influence upon the nature of hippocampal alterations provoked, suggesting that cytokines may differentially regulate hippocampal plasticity in neuropsychiatric conditions.Keywords: cytokine, depression, neuroplasticity, hippocampus, stressor |
format |
article |
author |
Julie Anne Seguin Jordan Brennan Emily Mangano Shawn Hayley |
author_facet |
Julie Anne Seguin Jordan Brennan Emily Mangano Shawn Hayley |
author_sort |
Julie Anne Seguin |
title |
Proinflammatory cytokines differentially influence adult hippocampal cell proliferation depending upon the route and chronicity of administration |
title_short |
Proinflammatory cytokines differentially influence adult hippocampal cell proliferation depending upon the route and chronicity of administration |
title_full |
Proinflammatory cytokines differentially influence adult hippocampal cell proliferation depending upon the route and chronicity of administration |
title_fullStr |
Proinflammatory cytokines differentially influence adult hippocampal cell proliferation depending upon the route and chronicity of administration |
title_full_unstemmed |
Proinflammatory cytokines differentially influence adult hippocampal cell proliferation depending upon the route and chronicity of administration |
title_sort |
proinflammatory cytokines differentially influence adult hippocampal cell proliferation depending upon the route and chronicity of administration |
publisher |
Dove Medical Press |
publishDate |
2008 |
url |
https://doaj.org/article/8031b6a09f6945babf33fe4350530e15 |
work_keys_str_mv |
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1718398553074696192 |