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Intranasal Delivery of Targeted Nanoparticles Loaded With miR-132 to Brain for the Treatment of Neurodegenerative Diseases

Effective treatments for neurodegenerative diseases need to be developed. MiR132 is abundantly expressed in the brain, and it modulates neuron morphology and plays a key role in maintaining neuron survival. Regulating miR132 can effectively improve the symptoms of Alzheimer’s disease. It can also re...

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Autores principales: Su, Yu, Sun, Bixi, Gao, Xiaoshu, Dong, Xinyue, Fu, Lanbo, Zhang, Yingxin, Li, Zhulin, Wang, Yue, Jiang, Hongyu, Han, Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7424054/
https://www.ncbi.nlm.nih.gov/pubmed/32848773
http://dx.doi.org/10.3389/fphar.2020.01165
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author Su, Yu
Sun, Bixi
Gao, Xiaoshu
Dong, Xinyue
Fu, Lanbo
Zhang, Yingxin
Li, Zhulin
Wang, Yue
Jiang, Hongyu
Han, Bing
author_facet Su, Yu
Sun, Bixi
Gao, Xiaoshu
Dong, Xinyue
Fu, Lanbo
Zhang, Yingxin
Li, Zhulin
Wang, Yue
Jiang, Hongyu
Han, Bing
author_sort Su, Yu
collection PubMed
description Effective treatments for neurodegenerative diseases need to be developed. MiR132 is abundantly expressed in the brain, and it modulates neuron morphology and plays a key role in maintaining neuron survival. Regulating miR132 can effectively improve the symptoms of Alzheimer’s disease. It can also reduce cell death after cerebral hemorrhage, improve the microenvironment of hematoma lesions and provide a certain protective effect from brain damage after cerebral ischemia. MiR132 has great potential in the treatment of cerebral ischemia and Alzheimer’s disease. To prevent the decline of miR132 of miR132 levels in the blood, we used mouse and rat models of Alzheimer’s disease with ischemic brain injury, and then delivered Wheat germ agglutinin (WGA)-NPs-miR132 intranasally to treat neurological damage after cerebral ischemia. Synaptic protein expression levels in Alzheimer’s mouse models increased significantly after administration. We propose that, nasal delivery of WGA-NPs-miR132 is an interesting novel therapeutic approach for the treatment of neurodegenerative diseases.
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spelling pubmed-74240542020-08-25 Intranasal Delivery of Targeted Nanoparticles Loaded With miR-132 to Brain for the Treatment of Neurodegenerative Diseases Su, Yu Sun, Bixi Gao, Xiaoshu Dong, Xinyue Fu, Lanbo Zhang, Yingxin Li, Zhulin Wang, Yue Jiang, Hongyu Han, Bing Front Pharmacol Pharmacology Effective treatments for neurodegenerative diseases need to be developed. MiR132 is abundantly expressed in the brain, and it modulates neuron morphology and plays a key role in maintaining neuron survival. Regulating miR132 can effectively improve the symptoms of Alzheimer’s disease. It can also reduce cell death after cerebral hemorrhage, improve the microenvironment of hematoma lesions and provide a certain protective effect from brain damage after cerebral ischemia. MiR132 has great potential in the treatment of cerebral ischemia and Alzheimer’s disease. To prevent the decline of miR132 of miR132 levels in the blood, we used mouse and rat models of Alzheimer’s disease with ischemic brain injury, and then delivered Wheat germ agglutinin (WGA)-NPs-miR132 intranasally to treat neurological damage after cerebral ischemia. Synaptic protein expression levels in Alzheimer’s mouse models increased significantly after administration. We propose that, nasal delivery of WGA-NPs-miR132 is an interesting novel therapeutic approach for the treatment of neurodegenerative diseases. Frontiers Media S.A. 2020-08-06 /pmc/articles/PMC7424054/ /pubmed/32848773 http://dx.doi.org/10.3389/fphar.2020.01165 Text en Copyright © 2020 Su, Sun, Gao, Dong, Fu, Zhang, Li, Wang, Jiang and Han 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 Pharmacology
Su, Yu
Sun, Bixi
Gao, Xiaoshu
Dong, Xinyue
Fu, Lanbo
Zhang, Yingxin
Li, Zhulin
Wang, Yue
Jiang, Hongyu
Han, Bing
Intranasal Delivery of Targeted Nanoparticles Loaded With miR-132 to Brain for the Treatment of Neurodegenerative Diseases
title Intranasal Delivery of Targeted Nanoparticles Loaded With miR-132 to Brain for the Treatment of Neurodegenerative Diseases
title_full Intranasal Delivery of Targeted Nanoparticles Loaded With miR-132 to Brain for the Treatment of Neurodegenerative Diseases
title_fullStr Intranasal Delivery of Targeted Nanoparticles Loaded With miR-132 to Brain for the Treatment of Neurodegenerative Diseases
title_full_unstemmed Intranasal Delivery of Targeted Nanoparticles Loaded With miR-132 to Brain for the Treatment of Neurodegenerative Diseases
title_short Intranasal Delivery of Targeted Nanoparticles Loaded With miR-132 to Brain for the Treatment of Neurodegenerative Diseases
title_sort intranasal delivery of targeted nanoparticles loaded with mir-132 to brain for the treatment of neurodegenerative diseases
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7424054/
https://www.ncbi.nlm.nih.gov/pubmed/32848773
http://dx.doi.org/10.3389/fphar.2020.01165
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