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Intranasal administration of dauricine loaded on graphene oxide: multi-target therapy for Alzheimer's disease
Alzheimer's disease (AD) is a degenerative disease of the central nervous system characterized by progressive cognitive and memory-related impairment. However, current therapeutic treatments have not proved sufficiently effective, mainly due to the complicated pathogenesis of the disease. In th...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7971267/ https://www.ncbi.nlm.nih.gov/pubmed/33729067 http://dx.doi.org/10.1080/10717544.2021.1895909 |
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author | Wang, Kaixuan Wang, Lingfeng Chen, Ling Peng, Chiwei Luo, Beijiao Mo, Jingxin Chen, Wei |
author_facet | Wang, Kaixuan Wang, Lingfeng Chen, Ling Peng, Chiwei Luo, Beijiao Mo, Jingxin Chen, Wei |
author_sort | Wang, Kaixuan |
collection | PubMed |
description | Alzheimer's disease (AD) is a degenerative disease of the central nervous system characterized by progressive cognitive and memory-related impairment. However, current therapeutic treatments have not proved sufficiently effective, mainly due to the complicated pathogenesis of the disease. In this study, a nano-formulation of graphene oxide (GO) loaded with dauricine (Dau) was investigated in terms of the combined anti-inflammatory and anti-oxidative stress effects of Dau and the inhibition of misfolding and aggregation of the amyloid-β (Aβ) protein by GO. Both in vivo and in vitro models were induced using Aβ(1-42), and the formulation was administered nasally in mice. The results showed that GO loaded with Dau greatly reduced oxidative stress through increasing superoxide dismutase levels and decreasing reactive oxygen species and malondialdehyde levels in vitro; it also alleviated the cognitive memory deficits and brain glial cell activation in mice with Aβ(1-42)-induced AD. This proved that GO loaded with Dau could protect against Aβ(1-42)-induced oxidative damage and apoptosis in both in vitro and in vivo AD models; therefore, GO loaded with Dau has the potential to be an effective and agent for the rapid treatment of AD. |
format | Online Article Text |
id | pubmed-7971267 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-79712672021-03-31 Intranasal administration of dauricine loaded on graphene oxide: multi-target therapy for Alzheimer's disease Wang, Kaixuan Wang, Lingfeng Chen, Ling Peng, Chiwei Luo, Beijiao Mo, Jingxin Chen, Wei Drug Deliv Research Article Alzheimer's disease (AD) is a degenerative disease of the central nervous system characterized by progressive cognitive and memory-related impairment. However, current therapeutic treatments have not proved sufficiently effective, mainly due to the complicated pathogenesis of the disease. In this study, a nano-formulation of graphene oxide (GO) loaded with dauricine (Dau) was investigated in terms of the combined anti-inflammatory and anti-oxidative stress effects of Dau and the inhibition of misfolding and aggregation of the amyloid-β (Aβ) protein by GO. Both in vivo and in vitro models were induced using Aβ(1-42), and the formulation was administered nasally in mice. The results showed that GO loaded with Dau greatly reduced oxidative stress through increasing superoxide dismutase levels and decreasing reactive oxygen species and malondialdehyde levels in vitro; it also alleviated the cognitive memory deficits and brain glial cell activation in mice with Aβ(1-42)-induced AD. This proved that GO loaded with Dau could protect against Aβ(1-42)-induced oxidative damage and apoptosis in both in vitro and in vivo AD models; therefore, GO loaded with Dau has the potential to be an effective and agent for the rapid treatment of AD. Taylor & Francis 2021-03-17 /pmc/articles/PMC7971267/ /pubmed/33729067 http://dx.doi.org/10.1080/10717544.2021.1895909 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Wang, Kaixuan Wang, Lingfeng Chen, Ling Peng, Chiwei Luo, Beijiao Mo, Jingxin Chen, Wei Intranasal administration of dauricine loaded on graphene oxide: multi-target therapy for Alzheimer's disease |
title | Intranasal administration of dauricine loaded on graphene oxide: multi-target therapy for Alzheimer's disease |
title_full | Intranasal administration of dauricine loaded on graphene oxide: multi-target therapy for Alzheimer's disease |
title_fullStr | Intranasal administration of dauricine loaded on graphene oxide: multi-target therapy for Alzheimer's disease |
title_full_unstemmed | Intranasal administration of dauricine loaded on graphene oxide: multi-target therapy for Alzheimer's disease |
title_short | Intranasal administration of dauricine loaded on graphene oxide: multi-target therapy for Alzheimer's disease |
title_sort | intranasal administration of dauricine loaded on graphene oxide: multi-target therapy for alzheimer's disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7971267/ https://www.ncbi.nlm.nih.gov/pubmed/33729067 http://dx.doi.org/10.1080/10717544.2021.1895909 |
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