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Cytoprotective effect of chlorogenic acid against α-synuclein-related toxicity in catecholaminergic PC12 cells

Parkinson’s disease is a major neurodegenerative disease involving the selective degeneration of dopaminergic neurons and α-synuclein containing Lewy bodies formation in the substantia nigra. Although α-synuclein is a key molecule for both dopaminergic neuron death and the formation of inclusion bod...

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Autores principales: Teraoka, Mari, Nakaso, Kazuhiro, Kusumoto, Chiaki, Katano, Satoshi, Tajima, Naoko, Yamashita, Atsushi, Zushi, Teppei, Ito, Satoru, Matsura, Tatsuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: the Society for Free Radical Research Japan 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3432822/
https://www.ncbi.nlm.nih.gov/pubmed/22962530
http://dx.doi.org/10.3164/jcbn.D-11-00030
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author Teraoka, Mari
Nakaso, Kazuhiro
Kusumoto, Chiaki
Katano, Satoshi
Tajima, Naoko
Yamashita, Atsushi
Zushi, Teppei
Ito, Satoru
Matsura, Tatsuya
author_facet Teraoka, Mari
Nakaso, Kazuhiro
Kusumoto, Chiaki
Katano, Satoshi
Tajima, Naoko
Yamashita, Atsushi
Zushi, Teppei
Ito, Satoru
Matsura, Tatsuya
author_sort Teraoka, Mari
collection PubMed
description Parkinson’s disease is a major neurodegenerative disease involving the selective degeneration of dopaminergic neurons and α-synuclein containing Lewy bodies formation in the substantia nigra. Although α-synuclein is a key molecule for both dopaminergic neuron death and the formation of inclusion bodies, the mechanism of α-synuclein induction of Parkinson’s disease-related pathogenesis is not understood. In the present study, we found that the interaction between dopamine and α-synuclein requires the oxidation of dopamine. Furthermore, we examined the protective effect of chlorogenic acid, a major polyphenol contained in coffee, against α-syn and dopamine-related toxicity. Chlorogenic acid inhibits several DA/α-synuclein-related phenomenon, including the oxidation of dopamine, the interaction of oxidized dopamine with α-synuclein, and the oligomerization of α-synuclein under dopamine existing conditions in vitro. Finally, we showed that the cytoprotective effect against α-synuclein-related toxicity in PC12 cells that can be controlled by the Tet-Off system. Although the induction of α-synuclein in catecholaminergic PC12 cells causes a decrease in cell viability, chlorogenic acid rescued this cytotoxicity significantly in a dose dependent manner. These results suggest that the interaction of oxidized DA with α-synuclein may be a novel therapeutic target for Parkinson’s disease, and polyphenols, including chlorogenic acid, are candidates as protective and preventive agents for Parkinson’s disease onset.
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spelling pubmed-34328222012-09-07 Cytoprotective effect of chlorogenic acid against α-synuclein-related toxicity in catecholaminergic PC12 cells Teraoka, Mari Nakaso, Kazuhiro Kusumoto, Chiaki Katano, Satoshi Tajima, Naoko Yamashita, Atsushi Zushi, Teppei Ito, Satoru Matsura, Tatsuya J Clin Biochem Nutr Original Article Parkinson’s disease is a major neurodegenerative disease involving the selective degeneration of dopaminergic neurons and α-synuclein containing Lewy bodies formation in the substantia nigra. Although α-synuclein is a key molecule for both dopaminergic neuron death and the formation of inclusion bodies, the mechanism of α-synuclein induction of Parkinson’s disease-related pathogenesis is not understood. In the present study, we found that the interaction between dopamine and α-synuclein requires the oxidation of dopamine. Furthermore, we examined the protective effect of chlorogenic acid, a major polyphenol contained in coffee, against α-syn and dopamine-related toxicity. Chlorogenic acid inhibits several DA/α-synuclein-related phenomenon, including the oxidation of dopamine, the interaction of oxidized dopamine with α-synuclein, and the oligomerization of α-synuclein under dopamine existing conditions in vitro. Finally, we showed that the cytoprotective effect against α-synuclein-related toxicity in PC12 cells that can be controlled by the Tet-Off system. Although the induction of α-synuclein in catecholaminergic PC12 cells causes a decrease in cell viability, chlorogenic acid rescued this cytotoxicity significantly in a dose dependent manner. These results suggest that the interaction of oxidized DA with α-synuclein may be a novel therapeutic target for Parkinson’s disease, and polyphenols, including chlorogenic acid, are candidates as protective and preventive agents for Parkinson’s disease onset. the Society for Free Radical Research Japan 2012-09 2012-04-06 /pmc/articles/PMC3432822/ /pubmed/22962530 http://dx.doi.org/10.3164/jcbn.D-11-00030 Text en Copyright © 2012 JCBN 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 work is properly cited.
spellingShingle Original Article
Teraoka, Mari
Nakaso, Kazuhiro
Kusumoto, Chiaki
Katano, Satoshi
Tajima, Naoko
Yamashita, Atsushi
Zushi, Teppei
Ito, Satoru
Matsura, Tatsuya
Cytoprotective effect of chlorogenic acid against α-synuclein-related toxicity in catecholaminergic PC12 cells
title Cytoprotective effect of chlorogenic acid against α-synuclein-related toxicity in catecholaminergic PC12 cells
title_full Cytoprotective effect of chlorogenic acid against α-synuclein-related toxicity in catecholaminergic PC12 cells
title_fullStr Cytoprotective effect of chlorogenic acid against α-synuclein-related toxicity in catecholaminergic PC12 cells
title_full_unstemmed Cytoprotective effect of chlorogenic acid against α-synuclein-related toxicity in catecholaminergic PC12 cells
title_short Cytoprotective effect of chlorogenic acid against α-synuclein-related toxicity in catecholaminergic PC12 cells
title_sort cytoprotective effect of chlorogenic acid against α-synuclein-related toxicity in catecholaminergic pc12 cells
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3432822/
https://www.ncbi.nlm.nih.gov/pubmed/22962530
http://dx.doi.org/10.3164/jcbn.D-11-00030
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