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Protective effects of Huang-Lian-Jie-Du-Tang against Aβ(25–35)-induced memory deficits and oxidative stress in rats
OBJECTIVE: Huang-Lian-Jie-Du-Tang (HLJDT), a traditional Chinese medicine, improves cognitive ability in rat models of Alzheimer’s disease (AD). The objective of this study was to evaluate the protective effects of HLJDT on learning and memory impairment that are caused by Aβ(25–35). METHODS: Rats w...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7133406/ https://www.ncbi.nlm.nih.gov/pubmed/32223685 http://dx.doi.org/10.1177/0300060519893859 |
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author | Wu, Wenbin He, Xiaojing Xie, Shuling Li, Bin Chen, Jinxin Qu, Yanqin Li, Baiyang Lei, Ming Liu, Xuehui |
author_facet | Wu, Wenbin He, Xiaojing Xie, Shuling Li, Bin Chen, Jinxin Qu, Yanqin Li, Baiyang Lei, Ming Liu, Xuehui |
author_sort | Wu, Wenbin |
collection | PubMed |
description | OBJECTIVE: Huang-Lian-Jie-Du-Tang (HLJDT), a traditional Chinese medicine, improves cognitive ability in rat models of Alzheimer’s disease (AD). The objective of this study was to evaluate the protective effects of HLJDT on learning and memory impairment that are caused by Aβ(25–35). METHODS: Rats were randomly assigned to the following groups: control (water), Aβ(25–35), donepezil hydrochloride 1.05 mg/kg, HLJDT 6 g/kg, HLJDT 3 g/kg, and HLJDT 1.5 g/kg and the corresponding drugs were administered for 28 days by oral gavage. HLJDT for the prevention of Aβ(25–35)-induced injury in rats and the underlying mechanisms were assessed. Aβ(25–35) and amyloid precursor protein (APP) levels were measured in the hippocampal specimens. Total superoxide dismutase (T-SOD), glutathione (GSH), and malondialdehyde (MDA) levels in the hippocampus were also measured. The ultrastructure of CA1 hippocampal region was observed using electron microscopy. RESULTS: HLJDT treatment ameliorated impaired learning and memory significantly, decreased Aβ(25–35), and APP levels in the hippocampus, increased T-SOD and GSH activity and decreased the MDA concentration, and alleviated the nuclear and cytoplasmic abnormalities of the hippocampal CA 1 region that were induced by Aβ(25–35) injection. CONCLUSIONS: HLJDT might decrease hippocampal vulnerability to Aβ(25–35), suggesting its potential neuroprotective effect in AD. |
format | Online Article Text |
id | pubmed-7133406 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-71334062020-04-13 Protective effects of Huang-Lian-Jie-Du-Tang against Aβ(25–35)-induced memory deficits and oxidative stress in rats Wu, Wenbin He, Xiaojing Xie, Shuling Li, Bin Chen, Jinxin Qu, Yanqin Li, Baiyang Lei, Ming Liu, Xuehui J Int Med Res Retrospective Clinical Research Report OBJECTIVE: Huang-Lian-Jie-Du-Tang (HLJDT), a traditional Chinese medicine, improves cognitive ability in rat models of Alzheimer’s disease (AD). The objective of this study was to evaluate the protective effects of HLJDT on learning and memory impairment that are caused by Aβ(25–35). METHODS: Rats were randomly assigned to the following groups: control (water), Aβ(25–35), donepezil hydrochloride 1.05 mg/kg, HLJDT 6 g/kg, HLJDT 3 g/kg, and HLJDT 1.5 g/kg and the corresponding drugs were administered for 28 days by oral gavage. HLJDT for the prevention of Aβ(25–35)-induced injury in rats and the underlying mechanisms were assessed. Aβ(25–35) and amyloid precursor protein (APP) levels were measured in the hippocampal specimens. Total superoxide dismutase (T-SOD), glutathione (GSH), and malondialdehyde (MDA) levels in the hippocampus were also measured. The ultrastructure of CA1 hippocampal region was observed using electron microscopy. RESULTS: HLJDT treatment ameliorated impaired learning and memory significantly, decreased Aβ(25–35), and APP levels in the hippocampus, increased T-SOD and GSH activity and decreased the MDA concentration, and alleviated the nuclear and cytoplasmic abnormalities of the hippocampal CA 1 region that were induced by Aβ(25–35) injection. CONCLUSIONS: HLJDT might decrease hippocampal vulnerability to Aβ(25–35), suggesting its potential neuroprotective effect in AD. SAGE Publications 2020-03-30 /pmc/articles/PMC7133406/ /pubmed/32223685 http://dx.doi.org/10.1177/0300060519893859 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Retrospective Clinical Research Report Wu, Wenbin He, Xiaojing Xie, Shuling Li, Bin Chen, Jinxin Qu, Yanqin Li, Baiyang Lei, Ming Liu, Xuehui Protective effects of Huang-Lian-Jie-Du-Tang against Aβ(25–35)-induced memory deficits and oxidative stress in rats |
title | Protective effects of Huang-Lian-Jie-Du-Tang against Aβ(25–35)-induced memory deficits and oxidative stress in rats |
title_full | Protective effects of Huang-Lian-Jie-Du-Tang against Aβ(25–35)-induced memory deficits and oxidative stress in rats |
title_fullStr | Protective effects of Huang-Lian-Jie-Du-Tang against Aβ(25–35)-induced memory deficits and oxidative stress in rats |
title_full_unstemmed | Protective effects of Huang-Lian-Jie-Du-Tang against Aβ(25–35)-induced memory deficits and oxidative stress in rats |
title_short | Protective effects of Huang-Lian-Jie-Du-Tang against Aβ(25–35)-induced memory deficits and oxidative stress in rats |
title_sort | protective effects of huang-lian-jie-du-tang against aβ(25–35)-induced memory deficits and oxidative stress in rats |
topic | Retrospective Clinical Research Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7133406/ https://www.ncbi.nlm.nih.gov/pubmed/32223685 http://dx.doi.org/10.1177/0300060519893859 |
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