Cargando…

Astrocytes in the Neuropathology of Bipolar Disorder: Review of Current Evidence

(1) Background: Approximately one-third of patients with bipolar disorder (BD) do not experience sustained remission with current treatments. Presently, astrocytes, i.e., glial cells that act as key regulators of neuroinflammation, have been a target for therapeutic development. Research regarding t...

Descripción completa

Detalles Bibliográficos
Autores principales: Dai, Nasia, Jones, Brett D. M., Husain, Muhammad Ishrat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9688542/
https://www.ncbi.nlm.nih.gov/pubmed/36358439
http://dx.doi.org/10.3390/brainsci12111513
_version_ 1784836294759677952
author Dai, Nasia
Jones, Brett D. M.
Husain, Muhammad Ishrat
author_facet Dai, Nasia
Jones, Brett D. M.
Husain, Muhammad Ishrat
author_sort Dai, Nasia
collection PubMed
description (1) Background: Approximately one-third of patients with bipolar disorder (BD) do not experience sustained remission with current treatments. Presently, astrocytes, i.e., glial cells that act as key regulators of neuroinflammation, have been a target for therapeutic development. Research regarding their role in the neuropathology of BD is limited. We conducted a scoping review on evidence linking astrocytes to the pathology of BD. (2) Methods: The search was conducted in MEDLINE for studies published from inception to August 2022. Studies of interest were data-extracted and reported based on the Preferred Reporting Items for Systematic Reviews and Meta-analysis Protocols. (3) Results: Overall, 650 publications were identified, of which 122 full texts were evaluated and 12 included. Four were in vitro, seven were ex vivo, and one study was both in vitro and in vivo. In vitro investigations focused on plasma levels of neuroinflammatory biomarkers S100B and glial fibrillary acidic protein (GFAP). Ex vivo investigations were post-mortem brain studies assessing astrocytes in regions of interest (i.e., anterior cingulate cortex, dorsolateral prefrontal cortex) using phosphorylated GFAP and ASCT-1. The in vivo and in vitro study evaluated morphological and chemical variations of YKL-40 between cohorts. (4) Conclusions: Reports indicate an association between astrocyte dysfunction and BD although larger studies are required to validate this association.
format Online
Article
Text
id pubmed-9688542
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-96885422022-11-25 Astrocytes in the Neuropathology of Bipolar Disorder: Review of Current Evidence Dai, Nasia Jones, Brett D. M. Husain, Muhammad Ishrat Brain Sci Review (1) Background: Approximately one-third of patients with bipolar disorder (BD) do not experience sustained remission with current treatments. Presently, astrocytes, i.e., glial cells that act as key regulators of neuroinflammation, have been a target for therapeutic development. Research regarding their role in the neuropathology of BD is limited. We conducted a scoping review on evidence linking astrocytes to the pathology of BD. (2) Methods: The search was conducted in MEDLINE for studies published from inception to August 2022. Studies of interest were data-extracted and reported based on the Preferred Reporting Items for Systematic Reviews and Meta-analysis Protocols. (3) Results: Overall, 650 publications were identified, of which 122 full texts were evaluated and 12 included. Four were in vitro, seven were ex vivo, and one study was both in vitro and in vivo. In vitro investigations focused on plasma levels of neuroinflammatory biomarkers S100B and glial fibrillary acidic protein (GFAP). Ex vivo investigations were post-mortem brain studies assessing astrocytes in regions of interest (i.e., anterior cingulate cortex, dorsolateral prefrontal cortex) using phosphorylated GFAP and ASCT-1. The in vivo and in vitro study evaluated morphological and chemical variations of YKL-40 between cohorts. (4) Conclusions: Reports indicate an association between astrocyte dysfunction and BD although larger studies are required to validate this association. MDPI 2022-11-08 /pmc/articles/PMC9688542/ /pubmed/36358439 http://dx.doi.org/10.3390/brainsci12111513 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Dai, Nasia
Jones, Brett D. M.
Husain, Muhammad Ishrat
Astrocytes in the Neuropathology of Bipolar Disorder: Review of Current Evidence
title Astrocytes in the Neuropathology of Bipolar Disorder: Review of Current Evidence
title_full Astrocytes in the Neuropathology of Bipolar Disorder: Review of Current Evidence
title_fullStr Astrocytes in the Neuropathology of Bipolar Disorder: Review of Current Evidence
title_full_unstemmed Astrocytes in the Neuropathology of Bipolar Disorder: Review of Current Evidence
title_short Astrocytes in the Neuropathology of Bipolar Disorder: Review of Current Evidence
title_sort astrocytes in the neuropathology of bipolar disorder: review of current evidence
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9688542/
https://www.ncbi.nlm.nih.gov/pubmed/36358439
http://dx.doi.org/10.3390/brainsci12111513
work_keys_str_mv AT dainasia astrocytesintheneuropathologyofbipolardisorderreviewofcurrentevidence
AT jonesbrettdm astrocytesintheneuropathologyofbipolardisorderreviewofcurrentevidence
AT husainmuhammadishrat astrocytesintheneuropathologyofbipolardisorderreviewofcurrentevidence