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COVID-19-induced neurological symptoms: focus on the role of metal ions

Neurological symptoms are prevalent in both the acute and post-acute phases of coronavirus disease 2019 (COVID-19), and they are becoming a major concern for the prognosis of COVID-19 patients. Accumulation evidence has suggested that metal ion disorders occur in the central nervous system (CNS) of...

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Autores principales: Zhang, Yi-Yue, Ren, Kai-Di, Luo, Xiu-Ju, Peng, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9996599/
https://www.ncbi.nlm.nih.gov/pubmed/36892679
http://dx.doi.org/10.1007/s10787-023-01176-2
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author Zhang, Yi-Yue
Ren, Kai-Di
Luo, Xiu-Ju
Peng, Jun
author_facet Zhang, Yi-Yue
Ren, Kai-Di
Luo, Xiu-Ju
Peng, Jun
author_sort Zhang, Yi-Yue
collection PubMed
description Neurological symptoms are prevalent in both the acute and post-acute phases of coronavirus disease 2019 (COVID-19), and they are becoming a major concern for the prognosis of COVID-19 patients. Accumulation evidence has suggested that metal ion disorders occur in the central nervous system (CNS) of COVID-19 patients. Metal ions participate in the development, metabolism, redox and neurotransmitter transmission in the CNS and are tightly regulated by metal ion channels. COVID-19 infection causes neurological metal disorders and metal ion channels abnormal switching, subsequently resulting in neuroinflammation, oxidative stress, excitotoxicity, neuronal cell death, and eventually eliciting a series of COVID-19-induced neurological symptoms. Therefore, metal homeostasis-related signaling pathways are emerging as promising therapeutic targets for mitigating COVID-19-induced neurological symptoms. This review provides a summary for the latest advances in research related to the physiological and pathophysiological functions of metal ions and metal ion channels, as well as their role in COVID-19-induced neurological symptoms. In addition, currently available modulators of metal ions and their channels are also discussed. Collectively, the current work offers a few recommendations according to published reports and in-depth reflections to ameliorate COVID-19-induced neurological symptoms. Further studies need to focus on the crosstalk and interactions between different metal ions and their channels. Simultaneous pharmacological intervention of two or more metal signaling pathway disorders may provide clinical advantages in treating COVID-19-induced neurological symptoms.
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spelling pubmed-99965992023-03-09 COVID-19-induced neurological symptoms: focus on the role of metal ions Zhang, Yi-Yue Ren, Kai-Di Luo, Xiu-Ju Peng, Jun Inflammopharmacology Review Neurological symptoms are prevalent in both the acute and post-acute phases of coronavirus disease 2019 (COVID-19), and they are becoming a major concern for the prognosis of COVID-19 patients. Accumulation evidence has suggested that metal ion disorders occur in the central nervous system (CNS) of COVID-19 patients. Metal ions participate in the development, metabolism, redox and neurotransmitter transmission in the CNS and are tightly regulated by metal ion channels. COVID-19 infection causes neurological metal disorders and metal ion channels abnormal switching, subsequently resulting in neuroinflammation, oxidative stress, excitotoxicity, neuronal cell death, and eventually eliciting a series of COVID-19-induced neurological symptoms. Therefore, metal homeostasis-related signaling pathways are emerging as promising therapeutic targets for mitigating COVID-19-induced neurological symptoms. This review provides a summary for the latest advances in research related to the physiological and pathophysiological functions of metal ions and metal ion channels, as well as their role in COVID-19-induced neurological symptoms. In addition, currently available modulators of metal ions and their channels are also discussed. Collectively, the current work offers a few recommendations according to published reports and in-depth reflections to ameliorate COVID-19-induced neurological symptoms. Further studies need to focus on the crosstalk and interactions between different metal ions and their channels. Simultaneous pharmacological intervention of two or more metal signaling pathway disorders may provide clinical advantages in treating COVID-19-induced neurological symptoms. Springer International Publishing 2023-03-09 2023 /pmc/articles/PMC9996599/ /pubmed/36892679 http://dx.doi.org/10.1007/s10787-023-01176-2 Text en © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Review
Zhang, Yi-Yue
Ren, Kai-Di
Luo, Xiu-Ju
Peng, Jun
COVID-19-induced neurological symptoms: focus on the role of metal ions
title COVID-19-induced neurological symptoms: focus on the role of metal ions
title_full COVID-19-induced neurological symptoms: focus on the role of metal ions
title_fullStr COVID-19-induced neurological symptoms: focus on the role of metal ions
title_full_unstemmed COVID-19-induced neurological symptoms: focus on the role of metal ions
title_short COVID-19-induced neurological symptoms: focus on the role of metal ions
title_sort covid-19-induced neurological symptoms: focus on the role of metal ions
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9996599/
https://www.ncbi.nlm.nih.gov/pubmed/36892679
http://dx.doi.org/10.1007/s10787-023-01176-2
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