4.7 Article

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

期刊

FRONTIERS IN PHARMACOLOGY
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2021.753548

关键词

circadian clock; intervertebral disc degeneration (IDD); (-)-epigallocatechin-3-gallate (EGCG); oxidative stress; Bmal1

资金

  1. National Natural Science Foundation of China [81972052, 81802143, 81672148]
  2. National Key Research and Development Plan [2016YFC1101700]
  3. National Basic Research Program of China (973 Program) [2014CB542206]
  4. Program for Changjiang Scholar and Innovative Research Team in University [IRT1053, IRT13051]
  5. China Postdoctoral Science Foundation [2019M653967]
  6. A Foundation for the Author of National Excellent Doctoral Dissertation of PR China [201480]

向作者/读者索取更多资源

The circadian clock is crucial for managing daily physiological and metabolic processes, and disturbances can lead to degenerative diseases. EGCG, a compound with antioxidant properties, has been found to have protective effects on intervertebral disc degeneration by entraining the biological clock. This study provides evidence that EGCG's protective effects on NPCs are related to the circadian clock and depend on the core clock gene Bmal1.
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 H2O2-induced extracellular matrix degradation in NPCs and inhibited H2O2-induced NPC apoptosis. Our in vivo experiments also confirmed this finding. Furthermore, EGCG attenuated H2O2-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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