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Tacrine-6-Ferulic Acid, a Novel Multifunctional Dimer, Inhibits Amyloid-β-Mediated Alzheimer's Disease-Associated Pathogenesis In Vitro and In Vivo
We have previously synthesized a series of hybrid compounds by linking ferulic acid to tacrine as multifunctional agents based on the hypotheses that Alzheimer's disease (AD) generates cholinergic deficiency and oxidative stress. Interestingly, we found that they may have potential pharmacologi...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3285653/ https://www.ncbi.nlm.nih.gov/pubmed/22384101 http://dx.doi.org/10.1371/journal.pone.0031921 |
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author | Pi, Rongbiao Mao, Xuexuan Chao, Xiaojuan Cheng, Zhiyi Liu, Mengfei Duan, Xiaolu Ye, Mingzhong Chen, Xiaohong Mei, Zhengrong Liu, Peiqing Li, Wenming Han, Yifan |
author_facet | Pi, Rongbiao Mao, Xuexuan Chao, Xiaojuan Cheng, Zhiyi Liu, Mengfei Duan, Xiaolu Ye, Mingzhong Chen, Xiaohong Mei, Zhengrong Liu, Peiqing Li, Wenming Han, Yifan |
author_sort | Pi, Rongbiao |
collection | PubMed |
description | We have previously synthesized a series of hybrid compounds by linking ferulic acid to tacrine as multifunctional agents based on the hypotheses that Alzheimer's disease (AD) generates cholinergic deficiency and oxidative stress. Interestingly, we found that they may have potential pharmacological activities for treating AD. Here we report for the first time that tacrine-6-ferulic acid (T6FA), one of these compounds, can prevent amyloid-β peptide (Aβ)-induced AD-associated pathological changes in vitro and in vivo. Our results showed that T6FA significantly inhibited auto- and acetylcholinesterase (AChE)-induced aggregation of Aβ(1–40) in vitro and blocked the cell death induced by Aβ(1–40) in PC12 cells. In an AD mouse model by the intracerebroventricular injection of Aβ(1–40), T6FA significantly improved the cognitive ability along with increasing choline acetyltransferase and superoxide dismutase activity, decreasing AChE activity and malondialdehyde level. Based on our findings, we conclude that T6FA may be a promising multifunctional drug candidate for AD. |
format | Online Article Text |
id | pubmed-3285653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32856532012-03-01 Tacrine-6-Ferulic Acid, a Novel Multifunctional Dimer, Inhibits Amyloid-β-Mediated Alzheimer's Disease-Associated Pathogenesis In Vitro and In Vivo Pi, Rongbiao Mao, Xuexuan Chao, Xiaojuan Cheng, Zhiyi Liu, Mengfei Duan, Xiaolu Ye, Mingzhong Chen, Xiaohong Mei, Zhengrong Liu, Peiqing Li, Wenming Han, Yifan PLoS One Research Article We have previously synthesized a series of hybrid compounds by linking ferulic acid to tacrine as multifunctional agents based on the hypotheses that Alzheimer's disease (AD) generates cholinergic deficiency and oxidative stress. Interestingly, we found that they may have potential pharmacological activities for treating AD. Here we report for the first time that tacrine-6-ferulic acid (T6FA), one of these compounds, can prevent amyloid-β peptide (Aβ)-induced AD-associated pathological changes in vitro and in vivo. Our results showed that T6FA significantly inhibited auto- and acetylcholinesterase (AChE)-induced aggregation of Aβ(1–40) in vitro and blocked the cell death induced by Aβ(1–40) in PC12 cells. In an AD mouse model by the intracerebroventricular injection of Aβ(1–40), T6FA significantly improved the cognitive ability along with increasing choline acetyltransferase and superoxide dismutase activity, decreasing AChE activity and malondialdehyde level. Based on our findings, we conclude that T6FA may be a promising multifunctional drug candidate for AD. Public Library of Science 2012-02-23 /pmc/articles/PMC3285653/ /pubmed/22384101 http://dx.doi.org/10.1371/journal.pone.0031921 Text en Pi et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Pi, Rongbiao Mao, Xuexuan Chao, Xiaojuan Cheng, Zhiyi Liu, Mengfei Duan, Xiaolu Ye, Mingzhong Chen, Xiaohong Mei, Zhengrong Liu, Peiqing Li, Wenming Han, Yifan Tacrine-6-Ferulic Acid, a Novel Multifunctional Dimer, Inhibits Amyloid-β-Mediated Alzheimer's Disease-Associated Pathogenesis In Vitro and In Vivo |
title | Tacrine-6-Ferulic Acid, a Novel Multifunctional Dimer, Inhibits Amyloid-β-Mediated Alzheimer's Disease-Associated Pathogenesis In Vitro and In Vivo
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title_full | Tacrine-6-Ferulic Acid, a Novel Multifunctional Dimer, Inhibits Amyloid-β-Mediated Alzheimer's Disease-Associated Pathogenesis In Vitro and In Vivo
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title_fullStr | Tacrine-6-Ferulic Acid, a Novel Multifunctional Dimer, Inhibits Amyloid-β-Mediated Alzheimer's Disease-Associated Pathogenesis In Vitro and In Vivo
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title_full_unstemmed | Tacrine-6-Ferulic Acid, a Novel Multifunctional Dimer, Inhibits Amyloid-β-Mediated Alzheimer's Disease-Associated Pathogenesis In Vitro and In Vivo
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title_short | Tacrine-6-Ferulic Acid, a Novel Multifunctional Dimer, Inhibits Amyloid-β-Mediated Alzheimer's Disease-Associated Pathogenesis In Vitro and In Vivo
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title_sort | tacrine-6-ferulic acid, a novel multifunctional dimer, inhibits amyloid-β-mediated alzheimer's disease-associated pathogenesis in vitro and in vivo |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3285653/ https://www.ncbi.nlm.nih.gov/pubmed/22384101 http://dx.doi.org/10.1371/journal.pone.0031921 |
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