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Mulberry Extracts Alleviate Aβ (25–35)-Induced Injury and Change the Gene Expression Profile in PC12 Cells
Mulberry, which contained high amounts of anthocyanins, has been used in traditional Chinese medicine. Mulberry fruit extracts (ME) have demonstrated the antioxidant activity and neuroprotection. The study was to investigate the neuroprotective efficacy of ME against β-amyloid 25–35- (Aβ (25–35)-) i...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4280656/ https://www.ncbi.nlm.nih.gov/pubmed/25580148 http://dx.doi.org/10.1155/2014/150617 |
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author | Song, Nan Yang, Hongpeng Pang, Wei Qie, Zhiwei Lu, Hao Tan, Long Li, Haiqiang Sun, Shoudan Lian, Fuzhi Qin, Chuan Jiang, Yugang |
author_facet | Song, Nan Yang, Hongpeng Pang, Wei Qie, Zhiwei Lu, Hao Tan, Long Li, Haiqiang Sun, Shoudan Lian, Fuzhi Qin, Chuan Jiang, Yugang |
author_sort | Song, Nan |
collection | PubMed |
description | Mulberry, which contained high amounts of anthocyanins, has been used in traditional Chinese medicine. Mulberry fruit extracts (ME) have demonstrated the antioxidant activity and neuroprotection. The study was to investigate the neuroprotective efficacy of ME against β-amyloid 25–35- (Aβ (25–35)-) induced PC12 cells injury. Cells preincubated with or without ME (200 μg/mL) for 24 h were treated with Aβ (25–35) (20 μmol/L) for another 24 h. Cell viability was assessed by MTT, gene expression profiles were examined by cDNA microarrays, and RT-PCR were used to confirm the results of microarray assays. ME pretreatment was found to neutralize the cytotoxicity and prevent Aβ (25–35)-induced cells injury. Analyses of gene expression profile revealed that genes involving cell adhesion, peptidase activity, cytokine activity, ion binding activity, and angiogenesis regulation were significantly modulated by ME pretreatment. Among those genes, Apaf1, Bace2, and Plcb4 were enriched in the “Alzheimer's disease-reference pathway” and downregulated after ME intervention. RT-PCR results showed that ME preincubation could significantly inhibit Aβ (25–35) increased mRNA levels of these three genes. Overall, ME pretreatment could substantially alleviate PC12 cells injury and downregulate expression of AD-related genes, such as Apaf1, Bace2, and Plcb4. This study has a great nutrigenomics interest and brings new and important light in the field of AD intervention. |
format | Online Article Text |
id | pubmed-4280656 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-42806562015-01-11 Mulberry Extracts Alleviate Aβ (25–35)-Induced Injury and Change the Gene Expression Profile in PC12 Cells Song, Nan Yang, Hongpeng Pang, Wei Qie, Zhiwei Lu, Hao Tan, Long Li, Haiqiang Sun, Shoudan Lian, Fuzhi Qin, Chuan Jiang, Yugang Evid Based Complement Alternat Med Research Article Mulberry, which contained high amounts of anthocyanins, has been used in traditional Chinese medicine. Mulberry fruit extracts (ME) have demonstrated the antioxidant activity and neuroprotection. The study was to investigate the neuroprotective efficacy of ME against β-amyloid 25–35- (Aβ (25–35)-) induced PC12 cells injury. Cells preincubated with or without ME (200 μg/mL) for 24 h were treated with Aβ (25–35) (20 μmol/L) for another 24 h. Cell viability was assessed by MTT, gene expression profiles were examined by cDNA microarrays, and RT-PCR were used to confirm the results of microarray assays. ME pretreatment was found to neutralize the cytotoxicity and prevent Aβ (25–35)-induced cells injury. Analyses of gene expression profile revealed that genes involving cell adhesion, peptidase activity, cytokine activity, ion binding activity, and angiogenesis regulation were significantly modulated by ME pretreatment. Among those genes, Apaf1, Bace2, and Plcb4 were enriched in the “Alzheimer's disease-reference pathway” and downregulated after ME intervention. RT-PCR results showed that ME preincubation could significantly inhibit Aβ (25–35) increased mRNA levels of these three genes. Overall, ME pretreatment could substantially alleviate PC12 cells injury and downregulate expression of AD-related genes, such as Apaf1, Bace2, and Plcb4. This study has a great nutrigenomics interest and brings new and important light in the field of AD intervention. Hindawi Publishing Corporation 2014 2014-12-17 /pmc/articles/PMC4280656/ /pubmed/25580148 http://dx.doi.org/10.1155/2014/150617 Text en Copyright © 2014 Nan Song et al. https://creativecommons.org/licenses/by/3.0/ 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 Song, Nan Yang, Hongpeng Pang, Wei Qie, Zhiwei Lu, Hao Tan, Long Li, Haiqiang Sun, Shoudan Lian, Fuzhi Qin, Chuan Jiang, Yugang Mulberry Extracts Alleviate Aβ (25–35)-Induced Injury and Change the Gene Expression Profile in PC12 Cells |
title | Mulberry Extracts Alleviate Aβ
(25–35)-Induced Injury and Change the Gene Expression Profile in PC12 Cells |
title_full | Mulberry Extracts Alleviate Aβ
(25–35)-Induced Injury and Change the Gene Expression Profile in PC12 Cells |
title_fullStr | Mulberry Extracts Alleviate Aβ
(25–35)-Induced Injury and Change the Gene Expression Profile in PC12 Cells |
title_full_unstemmed | Mulberry Extracts Alleviate Aβ
(25–35)-Induced Injury and Change the Gene Expression Profile in PC12 Cells |
title_short | Mulberry Extracts Alleviate Aβ
(25–35)-Induced Injury and Change the Gene Expression Profile in PC12 Cells |
title_sort | mulberry extracts alleviate aβ
(25–35)-induced injury and change the gene expression profile in pc12 cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4280656/ https://www.ncbi.nlm.nih.gov/pubmed/25580148 http://dx.doi.org/10.1155/2014/150617 |
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