Theoretical and Natural Science

- The Open Access Proceedings Series for Conferences


Theoretical and Natural Science

Vol. 20, 20 December 2023


Open Access | Article

Treatment of autism spectrum disorder by regulating neurotransmitters and modifying genes

Qixuan Yin * 1
1 Tianjin Yinghua Experimental School

* Author to whom correspondence should be addressed.

Theoretical and Natural Science, Vol. 20, 42-49
Published 20 December 2023. © 2023 The Author(s). Published by EWA Publishing
This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Citation Qixuan Yin. Treatment of autism spectrum disorder by regulating neurotransmitters and modifying genes. TNS (2023) Vol. 20: 42-49. DOI: 10.54254/2753-8818/20/20230711.

Abstract

Autism spectrum disorder (ASD) is a neurological and developmental disorder, which has many underlying causes, making it much more challenging to find an appropriate treatment to cure. It has been found that ASD is related to a wide variety of neurochemical changes, including GABA, oxytocin, and several monoamine neurotransmitters such as dopamine, norepinephrine, and serotonin. Since ASD is heterogeneous, precise technology such as PET, LP, iEEG, rs-fMRIs, and MRS had been emerged to discover the site of illness. It requires a persistent effort since the ASD phenotype is invertible instead of unchanged, which will be explained soon. Until now, only genetic modified virus (rAAV) have so far successfully incorporated with transduction and gene expression in vivo. However, whether the presence of neutralizing circulating antibodies will preclude intravenous administration is unsure. Instead of systemic delivery, intrathecal administration is discovered as a substitute, which can solve the problem and have advanced to a clinical trial. More gene therapies are hypothesized, for instance, using rAAV for gene replacement, ASOs for RNA knockdown, and CRISPR/Cas9 for gene editing. Unfortunately, these gene therapies still have a long way to go to overcome the restrictions. As a result, this research will analyze the different treatments for the ASD.

Keywords

monoamine neurotransmitters, heterogeneous, gene editing

References

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Data Availability

The datasets used and/or analyzed during the current study will be available from the authors upon reasonable request.

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Volume Title
Proceedings of the 3rd International Conference on Biological Engineering and Medical Science
ISBN (Print)
978-1-83558-213-8
ISBN (Online)
978-1-83558-214-5
Published Date
20 December 2023
Series
Theoretical and Natural Science
ISSN (Print)
2753-8818
ISSN (Online)
2753-8826
DOI
10.54254/2753-8818/20/20230711
Copyright
20 December 2023
Open Access
This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited

Copyright © 2023 EWA Publishing. Unless Otherwise Stated