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Beneficial Effects of Green Tea Catechins on Neurodegenerative Diseases

Tea is one of the most consumed beverages in the world. Green tea, black tea, and oolong tea are made from the same plant Camellia sinensis (L.) O. Kuntze. Among them, green tea has been the most extensively studied for beneficial effects on diseases including cancer, obesity, diabetes, and inflamma...

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Autores principales: Pervin, Monira, Unno, Keiko, Ohishi, Tomokazu, Tanabe, Hiroki, Miyoshi, Noriyuki, Nakamura, Yoriyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099654/
https://www.ncbi.nlm.nih.gov/pubmed/29843466
http://dx.doi.org/10.3390/molecules23061297
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author Pervin, Monira
Unno, Keiko
Ohishi, Tomokazu
Tanabe, Hiroki
Miyoshi, Noriyuki
Nakamura, Yoriyuki
author_facet Pervin, Monira
Unno, Keiko
Ohishi, Tomokazu
Tanabe, Hiroki
Miyoshi, Noriyuki
Nakamura, Yoriyuki
author_sort Pervin, Monira
collection PubMed
description Tea is one of the most consumed beverages in the world. Green tea, black tea, and oolong tea are made from the same plant Camellia sinensis (L.) O. Kuntze. Among them, green tea has been the most extensively studied for beneficial effects on diseases including cancer, obesity, diabetes, and inflammatory and neurodegenerative diseases. Several human observational and intervention studies have found beneficial effects of tea consumption on neurodegenerative impairment, such as cognitive dysfunction and memory loss. These studies supported the basis of tea’s preventive effects of Parkinson’s disease, but few studies have revealed such effects on Alzheimer’s disease. In contrast, several human studies have not reported these favorable effects with regard to tea. This discrepancy may be due to incomplete adjustment of confounding factors, including the method of quantifying consumption, beverage temperature, cigarette smoking, alcohol consumption, and differences in genetic and environmental factors, such as race, sex, age, and lifestyle. Thus, more rigorous human studies are required to understand the neuroprotective effect of tea. A number of laboratory experiments demonstrated the benefits of green tea and green tea catechins (GTCs), such as epigallocatechin gallate (EGCG), and proposed action mechanisms. The targets of GTCs include the abnormal accumulation of fibrous proteins, such as Aβ and α-synuclein, inflammation, elevated expression of pro-apoptotic proteins, and oxidative stress, which are associated with neuronal cell dysfunction and death in the cerebral cortex. Computational molecular docking analysis revealed how EGCG can prevent the accumulation of fibrous proteins. These findings suggest that GTCs have the potential to be used in the prevention and treatment of neurodegenerative diseases and could be useful for the development of new drugs.
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spelling pubmed-60996542018-11-13 Beneficial Effects of Green Tea Catechins on Neurodegenerative Diseases Pervin, Monira Unno, Keiko Ohishi, Tomokazu Tanabe, Hiroki Miyoshi, Noriyuki Nakamura, Yoriyuki Molecules Article Tea is one of the most consumed beverages in the world. Green tea, black tea, and oolong tea are made from the same plant Camellia sinensis (L.) O. Kuntze. Among them, green tea has been the most extensively studied for beneficial effects on diseases including cancer, obesity, diabetes, and inflammatory and neurodegenerative diseases. Several human observational and intervention studies have found beneficial effects of tea consumption on neurodegenerative impairment, such as cognitive dysfunction and memory loss. These studies supported the basis of tea’s preventive effects of Parkinson’s disease, but few studies have revealed such effects on Alzheimer’s disease. In contrast, several human studies have not reported these favorable effects with regard to tea. This discrepancy may be due to incomplete adjustment of confounding factors, including the method of quantifying consumption, beverage temperature, cigarette smoking, alcohol consumption, and differences in genetic and environmental factors, such as race, sex, age, and lifestyle. Thus, more rigorous human studies are required to understand the neuroprotective effect of tea. A number of laboratory experiments demonstrated the benefits of green tea and green tea catechins (GTCs), such as epigallocatechin gallate (EGCG), and proposed action mechanisms. The targets of GTCs include the abnormal accumulation of fibrous proteins, such as Aβ and α-synuclein, inflammation, elevated expression of pro-apoptotic proteins, and oxidative stress, which are associated with neuronal cell dysfunction and death in the cerebral cortex. Computational molecular docking analysis revealed how EGCG can prevent the accumulation of fibrous proteins. These findings suggest that GTCs have the potential to be used in the prevention and treatment of neurodegenerative diseases and could be useful for the development of new drugs. MDPI 2018-05-29 /pmc/articles/PMC6099654/ /pubmed/29843466 http://dx.doi.org/10.3390/molecules23061297 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Pervin, Monira
Unno, Keiko
Ohishi, Tomokazu
Tanabe, Hiroki
Miyoshi, Noriyuki
Nakamura, Yoriyuki
Beneficial Effects of Green Tea Catechins on Neurodegenerative Diseases
title Beneficial Effects of Green Tea Catechins on Neurodegenerative Diseases
title_full Beneficial Effects of Green Tea Catechins on Neurodegenerative Diseases
title_fullStr Beneficial Effects of Green Tea Catechins on Neurodegenerative Diseases
title_full_unstemmed Beneficial Effects of Green Tea Catechins on Neurodegenerative Diseases
title_short Beneficial Effects of Green Tea Catechins on Neurodegenerative Diseases
title_sort beneficial effects of green tea catechins on neurodegenerative diseases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099654/
https://www.ncbi.nlm.nih.gov/pubmed/29843466
http://dx.doi.org/10.3390/molecules23061297
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