A catechin-enriched green tea extract prevents glucose-induced survival reduction in Caenorhabditis elegans through sir-2.1 and uba-1 dependent hormesis

被引:17
作者
Deusing, Dorothe Jenni [1 ]
Winter, Sarah [1 ]
Kler, Adolf [2 ]
Kriesl, Erwin [2 ]
Bonnlaender, Bernd [2 ]
Wenzel, Uwe [1 ]
Fitzenberger, Elena [1 ]
机构
[1] Univ Giessen, Mol Nutr Res Interdisciplinary Res Ctr, D-35392 Giessen, Germany
[2] Plantextrakt GmbH & Co KG, D-91487 Vestenbergsgreuth, Germany
关键词
Glucose-induced toxicity; Green tea catechins; Caenorhabditis elegans; SIR-2.1; Proteasome; Hormesis; CELLULAR STRESS-RESPONSE; OXIDATIVE STRESS; LIFE-SPAN; EPIGALLOCATECHIN GALLATE; DIETARY POLYPHENOLS; MEV-1; MUTANT; RESISTANCE; IMPAIRMENT; PROTEASOME; ACTIVATORS;
D O I
10.1016/j.fitote.2015.03.005
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Hyperglycemia is a hallmark of diabetes mellitus which leads to the onset of complications in the long term. Green tea through its high content of polyphenolic catechins, on the other hand, is suggested to prevent or at least delay such detrimental complications. In the present study we fed the nematode Caenorhabditis elegans on a liquid medium supplemented with 10 mM glucose in the absence or presence of a catechin-enriched green tea extract (CEGTE). After exposure of young adults for 48 h survival was subsequently measured under heat stress at 37 degrees C Whereas CEGTE at 0.01% did not affect the survival of wild type nematodes, it completely reversed the glucose-induced survival reduction. Those effects were not achieved through the monomeric catechins included in CEGTE. RNA interference (RNAi) for sir-2.1 not only prevented the survival extension by CEGTE under simultaneous glucose exposure but also caused a further reduction of survival. Likewise, the knockdown of uba-1, encoding the only El -ubiquitin-activating enzyme in C. elegans, proved that UBA-1 is essential for the survival extension by CEGTE and that its loss of function changes CEGTE from a survival extending into a survival reducing extract. Stimulation of the proteasome by CEGTE was finally proven through measurements of the proteolytic cleavage of a fluorogenic peptide substrate. To conclude, our studies provide evidence that CEGTE reverses glucose-induced damage in C elegans through activation of adaptive responses mediated by SIR-2.1 and proteasomal degradation. The hormetic mode of action is revealed by a reduction of survival once the adaptive processes were blocked. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:163 / 170
页数:8
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