Homeostatic-like Potentiation of the Aversive Habenulo-raphe Pathway in an Animal Model of Post-stroke Depression

Stroke is the third leading cause of death and the primary cause of adult long-term disability in Canada. Despite advances in rehabilitation research, stroke survivors experience an unusually high incidence of depressive symptoms which undermine recovery outcomes by reducing patient motivation level...

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Main Author: Maillé, Sébastien
Other Authors: Beiques, Jean-Claude
Language:en
Published: Université d'Ottawa / University of Ottawa 2018
Subjects:
Online Access:http://hdl.handle.net/10393/37287
http://dx.doi.org/10.20381/ruor-21559
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spelling ndltd-uottawa.ca-oai-ruor.uottawa.ca-10393-372872018-02-27T05:09:53Z Homeostatic-like Potentiation of the Aversive Habenulo-raphe Pathway in an Animal Model of Post-stroke Depression Maillé, Sébastien Beiques, Jean-Claude Stroke Depression Habenula Dorsal Raphe Nucleus Prefrontal cortex Homeostatic plasticity Stroke is the third leading cause of death and the primary cause of adult long-term disability in Canada. Despite advances in rehabilitation research, stroke survivors experience an unusually high incidence of depressive symptoms which undermine recovery outcomes by reducing patient motivation levels. Human and animal studies have linked the incidence of post-stroke depression and the extent of prefrontal cortex (PFC) damage. The PFC and the lateral habenula (LHb) are limbic structures that are strongly connected to the serotonergic dorsal raphe nucleus (DRN), a key neuronal hub for mood regulation. We hypothesized that PFC stroke produces a depressive phenotype by triggering maladaptive reorganization in mood-related networks. We used viral and optogenetic strategies to functionally characterize PFC and LHb projections to DRN. Moreover, we found that PFC stroke causes a time-dependent remodeling of LHb inputs to DRN 5-HT neurons which results in altered postsynaptic glutamate receptor number and subunit composition. This remodeling likely reflects a homeostatic upregulation of LHb-DRN synapses in response to stroke-induced challenge to network activity. Since these synapses encode stress and aversion, potentiation of this pathway could contribute to depressive symptoms following stroke. However, more work will be needed to identify the behavioral and network-level consequences of altered LHb-DRN dynamics. Thus, a deeper understanding of circuit mechanisms implicated in post-stroke depression will provide insights into this disease and open new treatment avenues to improve recovery. 2018-02-26T15:54:33Z 2018 Thesis http://hdl.handle.net/10393/37287 http://dx.doi.org/10.20381/ruor-21559 en Université d'Ottawa / University of Ottawa
collection NDLTD
language en
sources NDLTD
topic Stroke
Depression
Habenula
Dorsal Raphe Nucleus
Prefrontal cortex
Homeostatic plasticity
spellingShingle Stroke
Depression
Habenula
Dorsal Raphe Nucleus
Prefrontal cortex
Homeostatic plasticity
Maillé, Sébastien
Homeostatic-like Potentiation of the Aversive Habenulo-raphe Pathway in an Animal Model of Post-stroke Depression
description Stroke is the third leading cause of death and the primary cause of adult long-term disability in Canada. Despite advances in rehabilitation research, stroke survivors experience an unusually high incidence of depressive symptoms which undermine recovery outcomes by reducing patient motivation levels. Human and animal studies have linked the incidence of post-stroke depression and the extent of prefrontal cortex (PFC) damage. The PFC and the lateral habenula (LHb) are limbic structures that are strongly connected to the serotonergic dorsal raphe nucleus (DRN), a key neuronal hub for mood regulation. We hypothesized that PFC stroke produces a depressive phenotype by triggering maladaptive reorganization in mood-related networks. We used viral and optogenetic strategies to functionally characterize PFC and LHb projections to DRN. Moreover, we found that PFC stroke causes a time-dependent remodeling of LHb inputs to DRN 5-HT neurons which results in altered postsynaptic glutamate receptor number and subunit composition. This remodeling likely reflects a homeostatic upregulation of LHb-DRN synapses in response to stroke-induced challenge to network activity. Since these synapses encode stress and aversion, potentiation of this pathway could contribute to depressive symptoms following stroke. However, more work will be needed to identify the behavioral and network-level consequences of altered LHb-DRN dynamics. Thus, a deeper understanding of circuit mechanisms implicated in post-stroke depression will provide insights into this disease and open new treatment avenues to improve recovery.
author2 Beiques, Jean-Claude
author_facet Beiques, Jean-Claude
Maillé, Sébastien
author Maillé, Sébastien
author_sort Maillé, Sébastien
title Homeostatic-like Potentiation of the Aversive Habenulo-raphe Pathway in an Animal Model of Post-stroke Depression
title_short Homeostatic-like Potentiation of the Aversive Habenulo-raphe Pathway in an Animal Model of Post-stroke Depression
title_full Homeostatic-like Potentiation of the Aversive Habenulo-raphe Pathway in an Animal Model of Post-stroke Depression
title_fullStr Homeostatic-like Potentiation of the Aversive Habenulo-raphe Pathway in an Animal Model of Post-stroke Depression
title_full_unstemmed Homeostatic-like Potentiation of the Aversive Habenulo-raphe Pathway in an Animal Model of Post-stroke Depression
title_sort homeostatic-like potentiation of the aversive habenulo-raphe pathway in an animal model of post-stroke depression
publisher Université d'Ottawa / University of Ottawa
publishDate 2018
url http://hdl.handle.net/10393/37287
http://dx.doi.org/10.20381/ruor-21559
work_keys_str_mv AT maillesebastien homeostaticlikepotentiationoftheaversivehabenuloraphepathwayinananimalmodelofpoststrokedepression
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