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Locus coeruleus-CA1 projections are involved in chronic depressive stress-induced hippocampal vulnerability to transient global ischaemia

Depression and transient ischaemic attack represent the common psychological and neurological diseases, respectively, and are tightly associated. However, studies of depression-affected ischaemic attack have been limited to epidemiological evidences, and the neural circuits underlying depression-mod...

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Autores principales: Zhang, Qian, Hu, Dian Xing, He, Feng, Li, Chun Yang, Qi, Guang Jian, Cai, Hong Wei, Li, Tong Xia, Ming, Jie, Zhang, Pei, Chen, Xiao Qian, Tian, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6610150/
https://www.ncbi.nlm.nih.gov/pubmed/31270312
http://dx.doi.org/10.1038/s41467-019-10795-9
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author Zhang, Qian
Hu, Dian Xing
He, Feng
Li, Chun Yang
Qi, Guang Jian
Cai, Hong Wei
Li, Tong Xia
Ming, Jie
Zhang, Pei
Chen, Xiao Qian
Tian, Bo
author_facet Zhang, Qian
Hu, Dian Xing
He, Feng
Li, Chun Yang
Qi, Guang Jian
Cai, Hong Wei
Li, Tong Xia
Ming, Jie
Zhang, Pei
Chen, Xiao Qian
Tian, Bo
author_sort Zhang, Qian
collection PubMed
description Depression and transient ischaemic attack represent the common psychological and neurological diseases, respectively, and are tightly associated. However, studies of depression-affected ischaemic attack have been limited to epidemiological evidences, and the neural circuits underlying depression-modulated ischaemic injury remain unknown. Here, we find that chronic social defeat stress (CSDS) and chronic footshock stress (CFS) exacerbate CA1 neuron loss and spatial learning/memory impairment after a short transient global ischaemia (TGI) attack in mice. Whole-brain mapping of direct outputs of locus coeruleus (LC)-tyrosine hydroxylase (TH, Th:) positive neurons reveals that LC-CA1 projections are decreased in CSDS or CFS mice. Furthermore, using designer receptors exclusively activated by designer drugs (DREADDs)-based chemogenetic tools, we determine that Th:LC-CA1 circuit is necessary and sufficient for depression-induced aggravated outcomes of TGI. Collectively, we suggest that Th:LC-CA1 pathway plays a crucial role in depression-induced TGI vulnerability and offers a potential intervention for preventing depression-related transient ischaemic attack.
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spelling pubmed-66101502019-07-08 Locus coeruleus-CA1 projections are involved in chronic depressive stress-induced hippocampal vulnerability to transient global ischaemia Zhang, Qian Hu, Dian Xing He, Feng Li, Chun Yang Qi, Guang Jian Cai, Hong Wei Li, Tong Xia Ming, Jie Zhang, Pei Chen, Xiao Qian Tian, Bo Nat Commun Article Depression and transient ischaemic attack represent the common psychological and neurological diseases, respectively, and are tightly associated. However, studies of depression-affected ischaemic attack have been limited to epidemiological evidences, and the neural circuits underlying depression-modulated ischaemic injury remain unknown. Here, we find that chronic social defeat stress (CSDS) and chronic footshock stress (CFS) exacerbate CA1 neuron loss and spatial learning/memory impairment after a short transient global ischaemia (TGI) attack in mice. Whole-brain mapping of direct outputs of locus coeruleus (LC)-tyrosine hydroxylase (TH, Th:) positive neurons reveals that LC-CA1 projections are decreased in CSDS or CFS mice. Furthermore, using designer receptors exclusively activated by designer drugs (DREADDs)-based chemogenetic tools, we determine that Th:LC-CA1 circuit is necessary and sufficient for depression-induced aggravated outcomes of TGI. Collectively, we suggest that Th:LC-CA1 pathway plays a crucial role in depression-induced TGI vulnerability and offers a potential intervention for preventing depression-related transient ischaemic attack. Nature Publishing Group UK 2019-07-03 /pmc/articles/PMC6610150/ /pubmed/31270312 http://dx.doi.org/10.1038/s41467-019-10795-9 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zhang, Qian
Hu, Dian Xing
He, Feng
Li, Chun Yang
Qi, Guang Jian
Cai, Hong Wei
Li, Tong Xia
Ming, Jie
Zhang, Pei
Chen, Xiao Qian
Tian, Bo
Locus coeruleus-CA1 projections are involved in chronic depressive stress-induced hippocampal vulnerability to transient global ischaemia
title Locus coeruleus-CA1 projections are involved in chronic depressive stress-induced hippocampal vulnerability to transient global ischaemia
title_full Locus coeruleus-CA1 projections are involved in chronic depressive stress-induced hippocampal vulnerability to transient global ischaemia
title_fullStr Locus coeruleus-CA1 projections are involved in chronic depressive stress-induced hippocampal vulnerability to transient global ischaemia
title_full_unstemmed Locus coeruleus-CA1 projections are involved in chronic depressive stress-induced hippocampal vulnerability to transient global ischaemia
title_short Locus coeruleus-CA1 projections are involved in chronic depressive stress-induced hippocampal vulnerability to transient global ischaemia
title_sort locus coeruleus-ca1 projections are involved in chronic depressive stress-induced hippocampal vulnerability to transient global ischaemia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6610150/
https://www.ncbi.nlm.nih.gov/pubmed/31270312
http://dx.doi.org/10.1038/s41467-019-10795-9
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