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Tanshinone IIA attenuates demyelination and promotes remyelination in A. cantonensis-infected BALB/c mice
Background: Angiostrongylus cantonensis infection can cause demyelination in the central nervous system, and there is no effective treatment. Methods: We used dexamethasone, Tanshinone IIA (TSIIA) and Cryptotanshinone(Two traditional Chinese medicine monomers) in combination with albendazole (AB, a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6775289/ https://www.ncbi.nlm.nih.gov/pubmed/31592236 http://dx.doi.org/10.7150/ijbs.35266 |
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author | Feng, Ying Feng, Feng Zheng, Cunjing Zhou, Zongpu Jiang, Meihua Liu, Zhen Xie, Fukang Sun, Xi Wu, Zhongdao |
author_facet | Feng, Ying Feng, Feng Zheng, Cunjing Zhou, Zongpu Jiang, Meihua Liu, Zhen Xie, Fukang Sun, Xi Wu, Zhongdao |
author_sort | Feng, Ying |
collection | PubMed |
description | Background: Angiostrongylus cantonensis infection can cause demyelination in the central nervous system, and there is no effective treatment. Methods: We used dexamethasone, Tanshinone IIA (TSIIA) and Cryptotanshinone(Two traditional Chinese medicine monomers) in combination with albendazole (AB, a standard anti-helminthic compound) to observe their therapeutic effect on demyelination in A. cantonensis-infected mice. Luxol fast blue staining and electron microscope of myelin sheath, Oligodendrocyte (OL) number and myelin basic protein (MBP) expression in brain was detected in above groups. Results: TSIIA+AB facilitated OL proliferation and significantly increased both myelin sheath thickness and the population of small-diameter axons. In addition, TSIIA treatment inhibited the expression of inflammation-related factors (interleukin [IL]-6, IL-1β, tumor necrosis factor [TNF]-α, inducible nitric oxide synthase [iNOS]) rather than inhibiting eosinophil infiltration in brain. TSIIA also decreased microglial activation and shifted their phenotype from M1 to M2. Conclusions: Taken together, these results provide evidence that TSIIA combined with AB may be an effective treatment for demyelination caused by A. cantonensis infection and other demyelinating diseases. |
format | Online Article Text |
id | pubmed-6775289 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-67752892019-10-07 Tanshinone IIA attenuates demyelination and promotes remyelination in A. cantonensis-infected BALB/c mice Feng, Ying Feng, Feng Zheng, Cunjing Zhou, Zongpu Jiang, Meihua Liu, Zhen Xie, Fukang Sun, Xi Wu, Zhongdao Int J Biol Sci Research Paper Background: Angiostrongylus cantonensis infection can cause demyelination in the central nervous system, and there is no effective treatment. Methods: We used dexamethasone, Tanshinone IIA (TSIIA) and Cryptotanshinone(Two traditional Chinese medicine monomers) in combination with albendazole (AB, a standard anti-helminthic compound) to observe their therapeutic effect on demyelination in A. cantonensis-infected mice. Luxol fast blue staining and electron microscope of myelin sheath, Oligodendrocyte (OL) number and myelin basic protein (MBP) expression in brain was detected in above groups. Results: TSIIA+AB facilitated OL proliferation and significantly increased both myelin sheath thickness and the population of small-diameter axons. In addition, TSIIA treatment inhibited the expression of inflammation-related factors (interleukin [IL]-6, IL-1β, tumor necrosis factor [TNF]-α, inducible nitric oxide synthase [iNOS]) rather than inhibiting eosinophil infiltration in brain. TSIIA also decreased microglial activation and shifted their phenotype from M1 to M2. Conclusions: Taken together, these results provide evidence that TSIIA combined with AB may be an effective treatment for demyelination caused by A. cantonensis infection and other demyelinating diseases. Ivyspring International Publisher 2019-08-19 /pmc/articles/PMC6775289/ /pubmed/31592236 http://dx.doi.org/10.7150/ijbs.35266 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Feng, Ying Feng, Feng Zheng, Cunjing Zhou, Zongpu Jiang, Meihua Liu, Zhen Xie, Fukang Sun, Xi Wu, Zhongdao Tanshinone IIA attenuates demyelination and promotes remyelination in A. cantonensis-infected BALB/c mice |
title | Tanshinone IIA attenuates demyelination and promotes remyelination in A. cantonensis-infected BALB/c mice |
title_full | Tanshinone IIA attenuates demyelination and promotes remyelination in A. cantonensis-infected BALB/c mice |
title_fullStr | Tanshinone IIA attenuates demyelination and promotes remyelination in A. cantonensis-infected BALB/c mice |
title_full_unstemmed | Tanshinone IIA attenuates demyelination and promotes remyelination in A. cantonensis-infected BALB/c mice |
title_short | Tanshinone IIA attenuates demyelination and promotes remyelination in A. cantonensis-infected BALB/c mice |
title_sort | tanshinone iia attenuates demyelination and promotes remyelination in a. cantonensis-infected balb/c mice |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6775289/ https://www.ncbi.nlm.nih.gov/pubmed/31592236 http://dx.doi.org/10.7150/ijbs.35266 |
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