Green tea extract containing enhanced levels of epimerized catechins attenuates scopolamine-induced memory impairment in mice.
Animals
Avoidance Learning
/ drug effects
Catechin
/ chemistry
Cell Line, Tumor
DNA Methylation
/ drug effects
Disease Models, Animal
Dose-Response Relationship, Drug
Hot Temperature
Humans
Male
Maze Learning
/ drug effects
Memory Disorders
/ drug therapy
Mice
Mice, Inbred ICR
Plant Extracts
/ administration & dosage
Scopolamine
Tea
/ chemistry
(−)-Epigallocatechin 3-O-Gallate
Cognitive function
Epimerization
Gallocatechin gallate
Green tea
Synaptophysin
Journal
Journal of ethnopharmacology
ISSN: 1872-7573
Titre abrégé: J Ethnopharmacol
Pays: Ireland
ID NLM: 7903310
Informations de publication
Date de publication:
10 Aug 2020
10 Aug 2020
Historique:
received:
16
01
2020
revised:
17
04
2020
accepted:
26
04
2020
pubmed:
4
5
2020
medline:
17
2
2021
entrez:
4
5
2020
Statut:
ppublish
Résumé
Green tea has been used as a traditional medicine to control brain function and digestion. Recent works suggest that drinking green tea could prevent cognitive function impairment. During tea manufacturing processes, such as brewing and sterilization, green tea catechins are epimerized. However, the effects of heat-epimerized catechins on cognitive function are still unknown. To take this advantage, we developed a new green tea extract, high temperature processed-green tea extract (HTP-GTE), which has a similar catechin composition to green tea beverages. This study aimed to investigate the effect of HTP-GTE on scopolamine-induced cognitive dysfunction and neuronal differentiation, and to elucidate its underlying mechanisms of action. The neuronal differentiation promoting effects of HTP-GTE in SH-SY5Y cells was assessed by evaluating neurite length and the expression level of synaptophysin. The DNA methylation status at the synaptophysin promoter was determined in differentiated SH-SY5Y cells and in the hippocampi of mice. HTP-GTE was administered for 10 days at doses of 30, 100 and 300 mg/kg (p.o.) to mice, and its effects on cognitive functions were measured by Y-maze and passive avoidance tests under scopolamine-induced cholinergic blockade state. HTP-GTE induced neuronal differentiation and neurite outgrowth via the upregulation of synaptophysin gene expression. These beneficial effects of HTP-GTE resulted from reducing DNA methylation levels at the synaptophysin promoter via the suppression of DNMT1 activity. The administration of HTP-GTE ameliorated cognitive impairments in a scopolamine-treated mouse model. These results suggest that HTP-GTE could alleviate cognitive impairment by regulating synaptophysin expression and DNA methylation levels. Taken together, HTP-GTE would be a promising treatment for the cognitive impairment observed in dysfunction of the cholinergic neurotransmitter system.
Identifiants
pubmed: 32360798
pii: S0378-8741(20)30213-0
doi: 10.1016/j.jep.2020.112923
pii:
doi:
Substances chimiques
Plant Extracts
0
Tea
0
Catechin
8R1V1STN48
Scopolamine
DL48G20X8X
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
112923Informations de copyright
Copyright © 2020 Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest None of the authors has any conflicts of interest regarding this study.