Novel application of brain-targeting polyphenol compounds in sleep deprivation-induced cognitive dysfunction

被引:44
|
作者
Zhao, Wei [1 ,4 ]
Wang, Jun [1 ,4 ]
Bi, Weina [1 ,4 ]
Ferruzzi, Mario [5 ]
Yemul, Shrishailam [1 ]
Freire, Daniel [1 ]
Mazzola, Paolo [1 ,6 ]
Ho, Lap [1 ,4 ]
Dubner, Lauren [1 ]
Pasinetti, Giulio Maria [1 ,2 ,3 ,4 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Neurol, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Dept Psychiat, New York, NY 10029 USA
[3] Icahn Sch Med Mt Sinai, Dept Geriatr, New York, NY 10029 USA
[4] James J Peter VA Med Ctr, Geriatr Res Educ Clin Ctr, Bronx, NY USA
[5] Purdue Univ, Dept Food Sci, W Lafayette, IN 47907 USA
[6] Univ Milano Bicocca, Dept Hlth Sci, Monza, Italy
关键词
Sleep deprivation; Polyphenols; Cognitive dysfunction; Resilience; Memory consolidation; GREEN TEA CATECHINS; ALZHEIMERS-DISEASE; MOUSE MODEL; SYNAPTIC PLASTICITY; S6; KINASE; MEMORY; METABOLISM; HIPPOCAMPUS; DISORDERS; PATHWAY;
D O I
10.1016/j.neuint.2015.07.023
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sleep deprivation produces deficits in hippocampal synaptic plasticity and hippocampal-dependent memory storage. Recent evidence suggests that sleep deprivation disrupts memory consolidation through multiple mechanisms, including the down-regulation of the cAMP-response element-binding protein (CREB) and of mammalian target of rapamycin (mTOR) signaling. In this study, we tested the effects of a Bioactive Dietary Polyphenol Preparation (BDPP), comprised of grape seed polyphenol extract, Concord grape juice, and resveratrol, on the attenuation of sleep deprivation-induced cognitive impairment. We found that BDPP significantly improves sleep deprivation-induced contextual memory deficits, possibly through the activation of CREB and mTOR signaling pathways. We also identified brain-available polyphenol metabolites from BDPP, among which quercetin-3-O-glucuronide activates CREB signaling and malvidin-3-O-glucoside activates mTOR signaling. In combination, quercetin and malvidin-glucoside significantly attenuated sleep deprivation-induced cognitive impairment in -a mouse model of acute sleep deprivation. Our data suggests the feasibility of using select brain-targeting polyphenol compounds derived from BDPP as potential therapeutic agents in promoting resilience against sleep deprivation-induced cognitive dysfunction. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:191 / 197
页数:7
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