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The Gut-Immune-Brain Axis in Autism Spectrum Disorders; A Focus on Amino Acids

Autism spectrum disorder (ASD) is a range of neurodevelopmental conditions that affect communication and social behavior. Besides social deficits, systemic inflammation, gastrointestinal immune-related problems, and changes in the gut microbiota composition are characteristic for people with ASD. An...

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Autores principales: van Sadelhoff, Joris H. J., Perez Pardo, Paula, Wu, Jiangbo, Garssen, Johan, van Bergenhenegouwen, Jeroen, Hogenkamp, Astrid, Hartog, Anita, Kraneveld, Aletta D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477881/
https://www.ncbi.nlm.nih.gov/pubmed/31057483
http://dx.doi.org/10.3389/fendo.2019.00247
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author van Sadelhoff, Joris H. J.
Perez Pardo, Paula
Wu, Jiangbo
Garssen, Johan
van Bergenhenegouwen, Jeroen
Hogenkamp, Astrid
Hartog, Anita
Kraneveld, Aletta D.
author_facet van Sadelhoff, Joris H. J.
Perez Pardo, Paula
Wu, Jiangbo
Garssen, Johan
van Bergenhenegouwen, Jeroen
Hogenkamp, Astrid
Hartog, Anita
Kraneveld, Aletta D.
author_sort van Sadelhoff, Joris H. J.
collection PubMed
description Autism spectrum disorder (ASD) is a range of neurodevelopmental conditions that affect communication and social behavior. Besides social deficits, systemic inflammation, gastrointestinal immune-related problems, and changes in the gut microbiota composition are characteristic for people with ASD. Animal models showed that these characteristics can induce ASD-associated behavior, suggesting an intimate relationship between the microbiota, gut, immune system and the brain in ASD. Multiple factors can contribute to the development of ASD, but mutations leading to enhanced activation of the mammalian target of rapamycin (mTOR) are reported frequently. Hyperactivation of mTOR leads to deficits in the communication between neurons in the brain and to immune impairments. Hence, mTOR might be a critical factor linking the gut-brain-immune axis in ASD. Pharmacological inhibition of mTOR is shown to improve ASD-associated behavior and immune functions, however, the clinical use is limited due to severe side reactions. Interestingly, studies have shown that mTOR activation can also be modified by nutritional stimuli, in particular by amino acids. Moreover, specific amino acids are demonstrated to inhibit inflammation, improve gut barrier function and to modify the microbiota composition. In this review we will discuss the gut-brain-immune axis in ASD and explore the potential of amino acids as a treatment option for ASD, either via modification of mTOR activity, the immune system or the gut microbiota composition.
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spelling pubmed-64778812019-05-03 The Gut-Immune-Brain Axis in Autism Spectrum Disorders; A Focus on Amino Acids van Sadelhoff, Joris H. J. Perez Pardo, Paula Wu, Jiangbo Garssen, Johan van Bergenhenegouwen, Jeroen Hogenkamp, Astrid Hartog, Anita Kraneveld, Aletta D. Front Endocrinol (Lausanne) Endocrinology Autism spectrum disorder (ASD) is a range of neurodevelopmental conditions that affect communication and social behavior. Besides social deficits, systemic inflammation, gastrointestinal immune-related problems, and changes in the gut microbiota composition are characteristic for people with ASD. Animal models showed that these characteristics can induce ASD-associated behavior, suggesting an intimate relationship between the microbiota, gut, immune system and the brain in ASD. Multiple factors can contribute to the development of ASD, but mutations leading to enhanced activation of the mammalian target of rapamycin (mTOR) are reported frequently. Hyperactivation of mTOR leads to deficits in the communication between neurons in the brain and to immune impairments. Hence, mTOR might be a critical factor linking the gut-brain-immune axis in ASD. Pharmacological inhibition of mTOR is shown to improve ASD-associated behavior and immune functions, however, the clinical use is limited due to severe side reactions. Interestingly, studies have shown that mTOR activation can also be modified by nutritional stimuli, in particular by amino acids. Moreover, specific amino acids are demonstrated to inhibit inflammation, improve gut barrier function and to modify the microbiota composition. In this review we will discuss the gut-brain-immune axis in ASD and explore the potential of amino acids as a treatment option for ASD, either via modification of mTOR activity, the immune system or the gut microbiota composition. Frontiers Media S.A. 2019-04-16 /pmc/articles/PMC6477881/ /pubmed/31057483 http://dx.doi.org/10.3389/fendo.2019.00247 Text en Copyright © 2019 van Sadelhoff, Perez Pardo, Wu, Garssen, van Bergenhenegouwen, Hogenkamp, Hartog and Kraneveld. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
van Sadelhoff, Joris H. J.
Perez Pardo, Paula
Wu, Jiangbo
Garssen, Johan
van Bergenhenegouwen, Jeroen
Hogenkamp, Astrid
Hartog, Anita
Kraneveld, Aletta D.
The Gut-Immune-Brain Axis in Autism Spectrum Disorders; A Focus on Amino Acids
title The Gut-Immune-Brain Axis in Autism Spectrum Disorders; A Focus on Amino Acids
title_full The Gut-Immune-Brain Axis in Autism Spectrum Disorders; A Focus on Amino Acids
title_fullStr The Gut-Immune-Brain Axis in Autism Spectrum Disorders; A Focus on Amino Acids
title_full_unstemmed The Gut-Immune-Brain Axis in Autism Spectrum Disorders; A Focus on Amino Acids
title_short The Gut-Immune-Brain Axis in Autism Spectrum Disorders; A Focus on Amino Acids
title_sort gut-immune-brain axis in autism spectrum disorders; a focus on amino acids
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477881/
https://www.ncbi.nlm.nih.gov/pubmed/31057483
http://dx.doi.org/10.3389/fendo.2019.00247
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