Therapeutic Efficacy of a Synthetic Brain-Targeted H 2 S Donor Cross-Linked Nanomicelle in Autism Spectrum Disorder Rats through Aerobic Glycolysis
Autism spectrum disorder (ASD) is characterized by cognitive inflexibility and social deficits, with a notably limited range of brain-targeted medications, particularly in the field of nanomedicine. Herein, we introduce the brain-targeted H S donor cross-linked nanomicelle, named mannose-PEG600-lipo...
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creator | Zhang, Changmei Yang, Lingyuan Wang, Feng Liu, Mingyuan Liu, Zehui Zou, Mingyang Wu, Lijie |
description | Autism spectrum disorder (ASD) is characterized by cognitive inflexibility and social deficits, with a notably limited range of brain-targeted medications, particularly in the field of nanomedicine. Herein, we introduce the brain-targeted H
S donor cross-linked nanomicelle, named mannose-PEG600-lipoic acid (Man-LA). Man-LA demonstrates enhanced stability and precise brain delivery by interacting with glucose transporter 1 (GLUT1) in astrocytes, facilitating a gradual release of H
S that is modulated by glutathione (GSH).
, studies suggest that Man-LA alleviates symptoms of ASD, correlating with increased expression of aerobic glycolysis enzymes, elevated lactate production, and higher H
S levels, while preventing damage to hippocampal neurons.
, Man-LA tightly binds to aldehyde dehydrogenase family 3 member B1 (
in astrocytes, upregulating its expression. This interaction promotes aerobic glycolysis and enhances lactate production. These findings suggest a connection between ASD deficits and the dysregulation of astrocytic aerobic glycolysis, underscoring the role of H
S. Identifying the
gene within aerobic glycolysis pathways provides a promising target for ASD treatment. |
format | Article |
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S donor cross-linked nanomicelle, named mannose-PEG600-lipoic acid (Man-LA). Man-LA demonstrates enhanced stability and precise brain delivery by interacting with glucose transporter 1 (GLUT1) in astrocytes, facilitating a gradual release of H
S that is modulated by glutathione (GSH).
, studies suggest that Man-LA alleviates symptoms of ASD, correlating with increased expression of aerobic glycolysis enzymes, elevated lactate production, and higher H
S levels, while preventing damage to hippocampal neurons.
, Man-LA tightly binds to aldehyde dehydrogenase family 3 member B1 (
in astrocytes, upregulating its expression. This interaction promotes aerobic glycolysis and enhances lactate production. These findings suggest a connection between ASD deficits and the dysregulation of astrocytic aerobic glycolysis, underscoring the role of H
S. Identifying the
gene within aerobic glycolysis pathways provides a promising target for ASD treatment.</description><identifier>EISSN: 1944-8252</identifier><identifier>PMID: 39693363</identifier><language>eng</language><publisher>United States</publisher><ispartof>ACS applied materials & interfaces, 2024-12</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0003-4490-9673</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39693363$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Changmei</creatorcontrib><creatorcontrib>Yang, Lingyuan</creatorcontrib><creatorcontrib>Wang, Feng</creatorcontrib><creatorcontrib>Liu, Mingyuan</creatorcontrib><creatorcontrib>Liu, Zehui</creatorcontrib><creatorcontrib>Zou, Mingyang</creatorcontrib><creatorcontrib>Wu, Lijie</creatorcontrib><title>Therapeutic Efficacy of a Synthetic Brain-Targeted H 2 S Donor Cross-Linked Nanomicelle in Autism Spectrum Disorder Rats through Aerobic Glycolysis</title><title>ACS applied materials & interfaces</title><addtitle>ACS Appl Mater Interfaces</addtitle><description>Autism spectrum disorder (ASD) is characterized by cognitive inflexibility and social deficits, with a notably limited range of brain-targeted medications, particularly in the field of nanomedicine. Herein, we introduce the brain-targeted H
S donor cross-linked nanomicelle, named mannose-PEG600-lipoic acid (Man-LA). Man-LA demonstrates enhanced stability and precise brain delivery by interacting with glucose transporter 1 (GLUT1) in astrocytes, facilitating a gradual release of H
S that is modulated by glutathione (GSH).
, studies suggest that Man-LA alleviates symptoms of ASD, correlating with increased expression of aerobic glycolysis enzymes, elevated lactate production, and higher H
S levels, while preventing damage to hippocampal neurons.
, Man-LA tightly binds to aldehyde dehydrogenase family 3 member B1 (
in astrocytes, upregulating its expression. This interaction promotes aerobic glycolysis and enhances lactate production. These findings suggest a connection between ASD deficits and the dysregulation of astrocytic aerobic glycolysis, underscoring the role of H
S. Identifying the
gene within aerobic glycolysis pathways provides a promising target for ASD treatment.</description><issn>1944-8252</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFj81OwzAQhC0kREvLK1T7ApFC3EbkWNpCD4gDyb1ynU1j6p9o1zn4OXhhggRnTiPNfJrR3Ij5Y7VeZ0_FppiJe-bPPC9lkW_uxExWZSVlKefiq-mR1IBjNBoOXWe00glCBwrq5GOPP_4zKeOzRtEFI7ZwhAJq2AcfCHYUmLM3469T8K58cEajtQjGw3YqZQf1gDrS6GBvOFCLBB8qMsSewnjpYYsUztPIq0062MSGl-K2U5bx4VcXYvVyaHbHbBjPDtvTQMYpSqe_F_Jf4BvFvlQ1</recordid><startdate>20241218</startdate><enddate>20241218</enddate><creator>Zhang, Changmei</creator><creator>Yang, Lingyuan</creator><creator>Wang, Feng</creator><creator>Liu, Mingyuan</creator><creator>Liu, Zehui</creator><creator>Zou, Mingyang</creator><creator>Wu, Lijie</creator><scope>NPM</scope><orcidid>https://orcid.org/0000-0003-4490-9673</orcidid></search><sort><creationdate>20241218</creationdate><title>Therapeutic Efficacy of a Synthetic Brain-Targeted H 2 S Donor Cross-Linked Nanomicelle in Autism Spectrum Disorder Rats through Aerobic Glycolysis</title><author>Zhang, Changmei ; Yang, Lingyuan ; Wang, Feng ; Liu, Mingyuan ; Liu, Zehui ; Zou, Mingyang ; Wu, Lijie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmed_primary_396933633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Changmei</creatorcontrib><creatorcontrib>Yang, Lingyuan</creatorcontrib><creatorcontrib>Wang, Feng</creatorcontrib><creatorcontrib>Liu, Mingyuan</creatorcontrib><creatorcontrib>Liu, Zehui</creatorcontrib><creatorcontrib>Zou, Mingyang</creatorcontrib><creatorcontrib>Wu, Lijie</creatorcontrib><collection>PubMed</collection><jtitle>ACS applied materials & interfaces</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Changmei</au><au>Yang, Lingyuan</au><au>Wang, Feng</au><au>Liu, Mingyuan</au><au>Liu, Zehui</au><au>Zou, Mingyang</au><au>Wu, Lijie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Therapeutic Efficacy of a Synthetic Brain-Targeted H 2 S Donor Cross-Linked Nanomicelle in Autism Spectrum Disorder Rats through Aerobic Glycolysis</atitle><jtitle>ACS applied materials & interfaces</jtitle><addtitle>ACS Appl Mater Interfaces</addtitle><date>2024-12-18</date><risdate>2024</risdate><eissn>1944-8252</eissn><abstract>Autism spectrum disorder (ASD) is characterized by cognitive inflexibility and social deficits, with a notably limited range of brain-targeted medications, particularly in the field of nanomedicine. Herein, we introduce the brain-targeted H
S donor cross-linked nanomicelle, named mannose-PEG600-lipoic acid (Man-LA). Man-LA demonstrates enhanced stability and precise brain delivery by interacting with glucose transporter 1 (GLUT1) in astrocytes, facilitating a gradual release of H
S that is modulated by glutathione (GSH).
, studies suggest that Man-LA alleviates symptoms of ASD, correlating with increased expression of aerobic glycolysis enzymes, elevated lactate production, and higher H
S levels, while preventing damage to hippocampal neurons.
, Man-LA tightly binds to aldehyde dehydrogenase family 3 member B1 (
in astrocytes, upregulating its expression. This interaction promotes aerobic glycolysis and enhances lactate production. These findings suggest a connection between ASD deficits and the dysregulation of astrocytic aerobic glycolysis, underscoring the role of H
S. Identifying the
gene within aerobic glycolysis pathways provides a promising target for ASD treatment.</abstract><cop>United States</cop><pmid>39693363</pmid><orcidid>https://orcid.org/0000-0003-4490-9673</orcidid></addata></record> |
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title | Therapeutic Efficacy of a Synthetic Brain-Targeted H 2 S Donor Cross-Linked Nanomicelle in Autism Spectrum Disorder Rats through Aerobic Glycolysis |
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