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Salidroside protects PC-12 cells against amyloid β-induced apoptosis by activation of the ERK1/2 and AKT signaling pathways
Alzheimer’s disease (AD) is one of the most frequent diseases in elderly people and causes high mortality. Its incidence is increasing annually and no effective therapeutic treatment currently exists. In the present study, salidroside, a major active ingredient of Rhodiola rosea, was able to protect...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6414153/ https://www.ncbi.nlm.nih.gov/pubmed/30720058 http://dx.doi.org/10.3892/ijmm.2019.4088 |
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author | Liao, Zheng-Luan Su, Heng Tan, Yun-Fei Qiu, Ya-Ju Zhu, Jun-Peng Chen, Yan Lin, Si-Si Wu, Ming-Hao Mao, Yan-Ping Hu, Jiao-Jiao Yu, En-Yan |
author_facet | Liao, Zheng-Luan Su, Heng Tan, Yun-Fei Qiu, Ya-Ju Zhu, Jun-Peng Chen, Yan Lin, Si-Si Wu, Ming-Hao Mao, Yan-Ping Hu, Jiao-Jiao Yu, En-Yan |
author_sort | Liao, Zheng-Luan |
collection | PubMed |
description | Alzheimer’s disease (AD) is one of the most frequent diseases in elderly people and causes high mortality. Its incidence is increasing annually and no effective therapeutic treatment currently exists. In the present study, salidroside, a major active ingredient of Rhodiola rosea, was able to protect PC-12 cells from the toxicity and apoptosis induced by AD inducer amyloid (A)β(1--42). Salidroside significantly protected PC-12 cells by inhibiting Aβ(1-42)-induced cytotoxicity and mitochondria-mediated endogenous caspase apoptotic pathways. Mechanistic studies demonstrated that salidroside significantly activated the extracellular signal regulated kinase (ERK)1/2 and protein kinase B (AKT) signaling pathways. This observation was further confirmed using the ERK1/2 inhibitor PD98059 and the AKT inhibitor LY294002, which demonstrated that salidroside promoted PC-12 cell survival and proliferation by activating the ERK1/2 and AKT signaling pathways. Salidroside is a therapeutic candidate for the treatment of AD and provides a basis for further drug development. |
format | Online Article Text |
id | pubmed-6414153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-64141532019-03-19 Salidroside protects PC-12 cells against amyloid β-induced apoptosis by activation of the ERK1/2 and AKT signaling pathways Liao, Zheng-Luan Su, Heng Tan, Yun-Fei Qiu, Ya-Ju Zhu, Jun-Peng Chen, Yan Lin, Si-Si Wu, Ming-Hao Mao, Yan-Ping Hu, Jiao-Jiao Yu, En-Yan Int J Mol Med Articles Alzheimer’s disease (AD) is one of the most frequent diseases in elderly people and causes high mortality. Its incidence is increasing annually and no effective therapeutic treatment currently exists. In the present study, salidroside, a major active ingredient of Rhodiola rosea, was able to protect PC-12 cells from the toxicity and apoptosis induced by AD inducer amyloid (A)β(1--42). Salidroside significantly protected PC-12 cells by inhibiting Aβ(1-42)-induced cytotoxicity and mitochondria-mediated endogenous caspase apoptotic pathways. Mechanistic studies demonstrated that salidroside significantly activated the extracellular signal regulated kinase (ERK)1/2 and protein kinase B (AKT) signaling pathways. This observation was further confirmed using the ERK1/2 inhibitor PD98059 and the AKT inhibitor LY294002, which demonstrated that salidroside promoted PC-12 cell survival and proliferation by activating the ERK1/2 and AKT signaling pathways. Salidroside is a therapeutic candidate for the treatment of AD and provides a basis for further drug development. D.A. Spandidos 2019-04 2019-02-01 /pmc/articles/PMC6414153/ /pubmed/30720058 http://dx.doi.org/10.3892/ijmm.2019.4088 Text en Copyright: © Liao et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Liao, Zheng-Luan Su, Heng Tan, Yun-Fei Qiu, Ya-Ju Zhu, Jun-Peng Chen, Yan Lin, Si-Si Wu, Ming-Hao Mao, Yan-Ping Hu, Jiao-Jiao Yu, En-Yan Salidroside protects PC-12 cells against amyloid β-induced apoptosis by activation of the ERK1/2 and AKT signaling pathways |
title | Salidroside protects PC-12 cells against amyloid β-induced apoptosis by activation of the ERK1/2 and AKT signaling pathways |
title_full | Salidroside protects PC-12 cells against amyloid β-induced apoptosis by activation of the ERK1/2 and AKT signaling pathways |
title_fullStr | Salidroside protects PC-12 cells against amyloid β-induced apoptosis by activation of the ERK1/2 and AKT signaling pathways |
title_full_unstemmed | Salidroside protects PC-12 cells against amyloid β-induced apoptosis by activation of the ERK1/2 and AKT signaling pathways |
title_short | Salidroside protects PC-12 cells against amyloid β-induced apoptosis by activation of the ERK1/2 and AKT signaling pathways |
title_sort | salidroside protects pc-12 cells against amyloid β-induced apoptosis by activation of the erk1/2 and akt signaling pathways |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6414153/ https://www.ncbi.nlm.nih.gov/pubmed/30720058 http://dx.doi.org/10.3892/ijmm.2019.4088 |
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