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Tanshinone IIA Alleviates the AD Phenotypes in APP and PS1 Transgenic Mice
Therapeutic approach for Alzheimer's disease (AD) is still deficient. To find active compounds from herbal medicine is of interest in the alleviation of AD symptoms. This study aimed to investigate the protective effects of Tanshinone IIA (TIIA) on memory performance and synaptic plasticity in...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4870344/ https://www.ncbi.nlm.nih.gov/pubmed/27274990 http://dx.doi.org/10.1155/2016/7631801 |
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author | Li, Fengling Han, Guosheng Wu, Kexiang |
author_facet | Li, Fengling Han, Guosheng Wu, Kexiang |
author_sort | Li, Fengling |
collection | PubMed |
description | Therapeutic approach for Alzheimer's disease (AD) is still deficient. To find active compounds from herbal medicine is of interest in the alleviation of AD symptoms. This study aimed to investigate the protective effects of Tanshinone IIA (TIIA) on memory performance and synaptic plasticity in a transgenic AD model at the early phase. 25–100 mg/kg TIIA (intraperitoneal injection, i.p.) was administered to the six-month-old APP and PS1 transgenic mice for 30 consecutive days. After treatment, spatial memory, synaptic plasticity, and related mechanisms were investigated. Our result showed that memory impairment in AD mice was mitigated by 50 and 100 mg/kg TIIA treatments. Hippocampal long-term potentiation was impaired in AD model but rescued by 100 mg/kg TIIA treatment. Mechanically, TIIA treatment reduced the accumulations of beta-amyloid 1–42, C-terminal fragments (CTFs), and p-Tau in the AD model. TIIA did not affect basal BDNF but promoted depolarization-induced BDNF synthesis in the AD mice. Taken together, TIIA repairs hippocampal LTP and memory, likely, through facilitating the clearance of AD-related proteins and activating synaptic BDNF synthesis. TIIA might be a candidate drug for AD treatment. |
format | Online Article Text |
id | pubmed-4870344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-48703442016-06-05 Tanshinone IIA Alleviates the AD Phenotypes in APP and PS1 Transgenic Mice Li, Fengling Han, Guosheng Wu, Kexiang Biomed Res Int Research Article Therapeutic approach for Alzheimer's disease (AD) is still deficient. To find active compounds from herbal medicine is of interest in the alleviation of AD symptoms. This study aimed to investigate the protective effects of Tanshinone IIA (TIIA) on memory performance and synaptic plasticity in a transgenic AD model at the early phase. 25–100 mg/kg TIIA (intraperitoneal injection, i.p.) was administered to the six-month-old APP and PS1 transgenic mice for 30 consecutive days. After treatment, spatial memory, synaptic plasticity, and related mechanisms were investigated. Our result showed that memory impairment in AD mice was mitigated by 50 and 100 mg/kg TIIA treatments. Hippocampal long-term potentiation was impaired in AD model but rescued by 100 mg/kg TIIA treatment. Mechanically, TIIA treatment reduced the accumulations of beta-amyloid 1–42, C-terminal fragments (CTFs), and p-Tau in the AD model. TIIA did not affect basal BDNF but promoted depolarization-induced BDNF synthesis in the AD mice. Taken together, TIIA repairs hippocampal LTP and memory, likely, through facilitating the clearance of AD-related proteins and activating synaptic BDNF synthesis. TIIA might be a candidate drug for AD treatment. Hindawi Publishing Corporation 2016 2016-05-04 /pmc/articles/PMC4870344/ /pubmed/27274990 http://dx.doi.org/10.1155/2016/7631801 Text en Copyright © 2016 Fengling Li et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Li, Fengling Han, Guosheng Wu, Kexiang Tanshinone IIA Alleviates the AD Phenotypes in APP and PS1 Transgenic Mice |
title | Tanshinone IIA Alleviates the AD Phenotypes in APP and PS1 Transgenic Mice |
title_full | Tanshinone IIA Alleviates the AD Phenotypes in APP and PS1 Transgenic Mice |
title_fullStr | Tanshinone IIA Alleviates the AD Phenotypes in APP and PS1 Transgenic Mice |
title_full_unstemmed | Tanshinone IIA Alleviates the AD Phenotypes in APP and PS1 Transgenic Mice |
title_short | Tanshinone IIA Alleviates the AD Phenotypes in APP and PS1 Transgenic Mice |
title_sort | tanshinone iia alleviates the ad phenotypes in app and ps1 transgenic mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4870344/ https://www.ncbi.nlm.nih.gov/pubmed/27274990 http://dx.doi.org/10.1155/2016/7631801 |
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