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HIV-associated synaptic degeneration

Human immunodeficiency virus (HIV) infection induces neuronal injuries, with almost 50% of infected individuals developing HIV-associated neurocognitive disorders (HAND). Although highly activate antiretroviral therapy (HAART) has significantly reduced the incidence of severe dementia, the overall p...

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Autores principales: Ru, Wenjuan, Tang, Shao-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5576336/
https://www.ncbi.nlm.nih.gov/pubmed/28851400
http://dx.doi.org/10.1186/s13041-017-0321-z
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author Ru, Wenjuan
Tang, Shao-Jun
author_facet Ru, Wenjuan
Tang, Shao-Jun
author_sort Ru, Wenjuan
collection PubMed
description Human immunodeficiency virus (HIV) infection induces neuronal injuries, with almost 50% of infected individuals developing HIV-associated neurocognitive disorders (HAND). Although highly activate antiretroviral therapy (HAART) has significantly reduced the incidence of severe dementia, the overall prevalence of HAND remains high. Synaptic degeneration is emerging as one of the most relevant neuropathologies associate with HAND. Previous studies have reported critical roles of viral proteins and inflammatory responses in this pathogenesis. Infected cells, including macrophages, microglia and astrocytes, may release viral proteins and other neurotoxins to stimulate neurons and cause excessive calcium influx, overproduction of free radicals and disruption of neurotransmitter hemostasis. The dysregulation of neural circuits likely leads to synaptic damage and loss. Identification of the specific mechanism of the synaptic degeneration may facilitate the development of effective therapeutic approaches to treat HAND.
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spelling pubmed-55763362017-08-31 HIV-associated synaptic degeneration Ru, Wenjuan Tang, Shao-Jun Mol Brain Review Human immunodeficiency virus (HIV) infection induces neuronal injuries, with almost 50% of infected individuals developing HIV-associated neurocognitive disorders (HAND). Although highly activate antiretroviral therapy (HAART) has significantly reduced the incidence of severe dementia, the overall prevalence of HAND remains high. Synaptic degeneration is emerging as one of the most relevant neuropathologies associate with HAND. Previous studies have reported critical roles of viral proteins and inflammatory responses in this pathogenesis. Infected cells, including macrophages, microglia and astrocytes, may release viral proteins and other neurotoxins to stimulate neurons and cause excessive calcium influx, overproduction of free radicals and disruption of neurotransmitter hemostasis. The dysregulation of neural circuits likely leads to synaptic damage and loss. Identification of the specific mechanism of the synaptic degeneration may facilitate the development of effective therapeutic approaches to treat HAND. BioMed Central 2017-08-29 /pmc/articles/PMC5576336/ /pubmed/28851400 http://dx.doi.org/10.1186/s13041-017-0321-z Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Ru, Wenjuan
Tang, Shao-Jun
HIV-associated synaptic degeneration
title HIV-associated synaptic degeneration
title_full HIV-associated synaptic degeneration
title_fullStr HIV-associated synaptic degeneration
title_full_unstemmed HIV-associated synaptic degeneration
title_short HIV-associated synaptic degeneration
title_sort hiv-associated synaptic degeneration
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5576336/
https://www.ncbi.nlm.nih.gov/pubmed/28851400
http://dx.doi.org/10.1186/s13041-017-0321-z
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