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(-)-Epigallocatechin-3-gallate Ameliorates Intervertebral Disc Degeneration Through Reprogramming of the Circadian Clock

The circadian clock is vital in the management of our daily physiological as well as metabolic processes. Disturbances of the clock can cause degenerative and age-related diseases. Increasing evidence has indicated that the intervertebral discs contain an internal biological clock related to degener...

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Autores principales: Mei, Liangwei, Zheng, Yi, Ma, Teng, Xia, Bing, Gao, Xue, Hao, Yiming, Luo, Zhuojing, Huang, Jinghui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8599576/
https://www.ncbi.nlm.nih.gov/pubmed/34803694
http://dx.doi.org/10.3389/fphar.2021.753548
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author Mei, Liangwei
Zheng, Yi
Ma, Teng
Xia, Bing
Gao, Xue
Hao, Yiming
Luo, Zhuojing
Huang, Jinghui
author_facet Mei, Liangwei
Zheng, Yi
Ma, Teng
Xia, Bing
Gao, Xue
Hao, Yiming
Luo, Zhuojing
Huang, Jinghui
author_sort Mei, Liangwei
collection PubMed
description The circadian clock is vital in the management of our daily physiological as well as metabolic processes. Disturbances of the clock can cause degenerative and age-related diseases. Increasing evidence has indicated that the intervertebral discs contain an internal biological clock related to degeneration. However, to date, no bioactive compounds have been found that can ameliorate intervertebral disc degeneration (IDD) by restoring the circadian clock. (-)-Epigallocatechin-3-gallate (EGCG) is a nutritious food with powerful antioxidant properties, as well as entraining biological clock to improve health. The purpose of this study was to determine whether the protective effects of EGCG on nucleus pulposus (NPCs) under oxidative stress is related to the circadian clock. First, we found that EGCG attenuated H(2)O(2)-induced extracellular matrix degradation in NPCs and inhibited H(2)O(2)-induced NPC apoptosis. Our in vivo experiments also confirmed this finding. Furthermore, EGCG attenuated H(2)O(2)-triggered dampening of phase shifts and daily oscillations in circadian clock gene transcription as well as protein expression levels. Intriguingly, core clock gene (Bmal1) knockdown notably blocked the protective effects of EGCG. To our knowledge, this study provides the first convincing evidence that EGCG prevents IDD in a Bmal1-dependent manner. In general, EGCG supplementation can be used as a nutritional prevention strategy for the rehabilitation of degenerative diseases related to the circadian clock.
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spelling pubmed-85995762021-11-19 (-)-Epigallocatechin-3-gallate Ameliorates Intervertebral Disc Degeneration Through Reprogramming of the Circadian Clock Mei, Liangwei Zheng, Yi Ma, Teng Xia, Bing Gao, Xue Hao, Yiming Luo, Zhuojing Huang, Jinghui Front Pharmacol Pharmacology The circadian clock is vital in the management of our daily physiological as well as metabolic processes. Disturbances of the clock can cause degenerative and age-related diseases. Increasing evidence has indicated that the intervertebral discs contain an internal biological clock related to degeneration. However, to date, no bioactive compounds have been found that can ameliorate intervertebral disc degeneration (IDD) by restoring the circadian clock. (-)-Epigallocatechin-3-gallate (EGCG) is a nutritious food with powerful antioxidant properties, as well as entraining biological clock to improve health. The purpose of this study was to determine whether the protective effects of EGCG on nucleus pulposus (NPCs) under oxidative stress is related to the circadian clock. First, we found that EGCG attenuated H(2)O(2)-induced extracellular matrix degradation in NPCs and inhibited H(2)O(2)-induced NPC apoptosis. Our in vivo experiments also confirmed this finding. Furthermore, EGCG attenuated H(2)O(2)-triggered dampening of phase shifts and daily oscillations in circadian clock gene transcription as well as protein expression levels. Intriguingly, core clock gene (Bmal1) knockdown notably blocked the protective effects of EGCG. To our knowledge, this study provides the first convincing evidence that EGCG prevents IDD in a Bmal1-dependent manner. In general, EGCG supplementation can be used as a nutritional prevention strategy for the rehabilitation of degenerative diseases related to the circadian clock. Frontiers Media S.A. 2021-11-04 /pmc/articles/PMC8599576/ /pubmed/34803694 http://dx.doi.org/10.3389/fphar.2021.753548 Text en Copyright © 2021 Mei, Zheng, Ma, Xia, Gao, Hao, Luo and Huang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Mei, Liangwei
Zheng, Yi
Ma, Teng
Xia, Bing
Gao, Xue
Hao, Yiming
Luo, Zhuojing
Huang, Jinghui
(-)-Epigallocatechin-3-gallate Ameliorates Intervertebral Disc Degeneration Through Reprogramming of the Circadian Clock
title (-)-Epigallocatechin-3-gallate Ameliorates Intervertebral Disc Degeneration Through Reprogramming of the Circadian Clock
title_full (-)-Epigallocatechin-3-gallate Ameliorates Intervertebral Disc Degeneration Through Reprogramming of the Circadian Clock
title_fullStr (-)-Epigallocatechin-3-gallate Ameliorates Intervertebral Disc Degeneration Through Reprogramming of the Circadian Clock
title_full_unstemmed (-)-Epigallocatechin-3-gallate Ameliorates Intervertebral Disc Degeneration Through Reprogramming of the Circadian Clock
title_short (-)-Epigallocatechin-3-gallate Ameliorates Intervertebral Disc Degeneration Through Reprogramming of the Circadian Clock
title_sort (-)-epigallocatechin-3-gallate ameliorates intervertebral disc degeneration through reprogramming of the circadian clock
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8599576/
https://www.ncbi.nlm.nih.gov/pubmed/34803694
http://dx.doi.org/10.3389/fphar.2021.753548
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