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A Wholistic View of How Bumetanide Attenuates Autism Spectrum Disorders

The specific NKCC1 cotransporter antagonist, bumetanide, attenuates the severity of Autism Spectrum Disorders (ASD), and many neurodevelopmental or neurodegenerative disorders in animal models and clinical trials. However, the pervasive expression of NKCC1 in many cell types throughout the body is t...

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Autores principales: Delpire, Eric, Ben-Ari, Yehezkel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9367773/
https://www.ncbi.nlm.nih.gov/pubmed/35954263
http://dx.doi.org/10.3390/cells11152419
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author Delpire, Eric
Ben-Ari, Yehezkel
author_facet Delpire, Eric
Ben-Ari, Yehezkel
author_sort Delpire, Eric
collection PubMed
description The specific NKCC1 cotransporter antagonist, bumetanide, attenuates the severity of Autism Spectrum Disorders (ASD), and many neurodevelopmental or neurodegenerative disorders in animal models and clinical trials. However, the pervasive expression of NKCC1 in many cell types throughout the body is thought to challenge the therapeutic efficacy of bumetanide. However, many peripheral functions, including intestinal, metabolic, or vascular, etc., are perturbed in brain disorders contributing to the neurological sequels. Alterations of these functions also increase the incidence of the disorder suggesting complex bidirectional links with the clinical manifestations. We suggest that a more holistic view of ASD and other disorders is warranted to account for the multiple sites impacted by the original intra-uterine insult. From this perspective, large-spectrum active repositioned drugs that act centrally and peripherally might constitute a useful approach to treating these disorders.
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spelling pubmed-93677732022-08-12 A Wholistic View of How Bumetanide Attenuates Autism Spectrum Disorders Delpire, Eric Ben-Ari, Yehezkel Cells Commentary The specific NKCC1 cotransporter antagonist, bumetanide, attenuates the severity of Autism Spectrum Disorders (ASD), and many neurodevelopmental or neurodegenerative disorders in animal models and clinical trials. However, the pervasive expression of NKCC1 in many cell types throughout the body is thought to challenge the therapeutic efficacy of bumetanide. However, many peripheral functions, including intestinal, metabolic, or vascular, etc., are perturbed in brain disorders contributing to the neurological sequels. Alterations of these functions also increase the incidence of the disorder suggesting complex bidirectional links with the clinical manifestations. We suggest that a more holistic view of ASD and other disorders is warranted to account for the multiple sites impacted by the original intra-uterine insult. From this perspective, large-spectrum active repositioned drugs that act centrally and peripherally might constitute a useful approach to treating these disorders. MDPI 2022-08-04 /pmc/articles/PMC9367773/ /pubmed/35954263 http://dx.doi.org/10.3390/cells11152419 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 Commentary
Delpire, Eric
Ben-Ari, Yehezkel
A Wholistic View of How Bumetanide Attenuates Autism Spectrum Disorders
title A Wholistic View of How Bumetanide Attenuates Autism Spectrum Disorders
title_full A Wholistic View of How Bumetanide Attenuates Autism Spectrum Disorders
title_fullStr A Wholistic View of How Bumetanide Attenuates Autism Spectrum Disorders
title_full_unstemmed A Wholistic View of How Bumetanide Attenuates Autism Spectrum Disorders
title_short A Wholistic View of How Bumetanide Attenuates Autism Spectrum Disorders
title_sort wholistic view of how bumetanide attenuates autism spectrum disorders
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9367773/
https://www.ncbi.nlm.nih.gov/pubmed/35954263
http://dx.doi.org/10.3390/cells11152419
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