Open access · CC-BY
via OpenAlex
Green tea catechins EGCG and ECG enhance the fitness and lifespan of Caenorhabditis elegans by complex I inhibition
Jing Tian, Caroline Geiss, Kim Zarse, Corina T. Madreiter‐Sokolowski, Michael Ristow
Aging · 2021 · ▲ 75 citations
Deregulated nutrient-sensing
Mitochondrial dysfunction
Altered intercellular communication
Exercise
C. elegans
Mouse
Abstract
Green tea catechins are associated with a delay in aging. We have designed the current study to investigate the impact and to unveil the target of the most abundant green tea catechins, epigallocatechin gallate (EGCG) and epicatechin gallate (ECG). Experiments were performed in Caenorhabditis elegans to analyze cellular metabolism, ROS homeostasis, stress resistance, physical exercise capacity, health- and lifespan, and the underlying signaling pathways. Besides, we examined the impact of EGCG and ECG in isolated murine mitochondria. A concentration of 2.5 μM EGCG and ECG enhanced health- and lifespan as well as stress resistance in C. elegans. Catechins hampered mitochondrial respiration in C. elegans after 6â12 h and the activity of complex I in isolated rodent mitochondria. The impaired mitochondrial respiration was accompanied by a transient drop in ATP production and a temporary increase in ROS levels in C. elegans. After 24 h, mitochondrial respiration and ATP levels got restored, and ROS levels even dropped below control conditions. The lifespan increases induced by EGCG and ECG were dependent on AAK-2/AMPK and SIR-2.1/SIRT1, as well as on PMK-1/p38 MAPK, SKN-1/NRF2, and DAF-16/FOXO. Long-term effects included significantly diminished fat content and enhanced SOD and CAT activities, required for the positive impact of catechins on lifespan. In summary, complex I inhibition by EGCG and ECG induced a transient drop in cellular ATP levels and a temporary ROS burst, resulting in SKN-1 and DAF-16 activation. Through adaptative responses, catechins reduced fat content, enhanced ROS defense, and improved healthspan(definition) in the long term.
◌ CITATION ONLY
Full text is not openly licensed for redistribution here. Read it at the source:
Provenance
- Source
- OpenAlex
- DOI
- 10.18632/aging.203597
- Canonical
- link ↗
- Fetched
- 2026-06-28 MST
Cite this
APA
Tian, J., Geiss, C., Zarse, K., Madreiter‐Sokolowski, C.T., & Ristow, M. (2021). Green tea catechins EGCG and ECG enhance the fitness and lifespan of Caenorhabditis elegans by complex I inhibition. <em>Aging</em>. https://doi.org/10.18632/aging.203597
Vancouver
Tian J, Geiss C, Zarse K, Madreiter‐Sokolowski CT, Ristow M. Green tea catechins EGCG and ECG enhance the fitness and lifespan of Caenorhabditis elegans by complex I inhibition. Aging. 2021. doi:10.18632/aging.203597.
BibTeX
@article{jing2021Greent,
title = {Green tea catechins EGCG and ECG enhance the fitness and lifespan of Caenorhabditis elegans by complex I inhibition},
author = {Jing Tian and Caroline Geiss and Kim Zarse and Corina T. Madreiter‐Sokolowski and Michael Ristow},
journal = {Aging},
year = {2021},
doi = {10.18632/aging.203597},
}
Research neighborhood
References, citing works, and semantically nearest findings. Click a node to open it.
Related findings
Molecular Metabolism 2013
Open access · CC-BY
Neuronal ROS signaling rather than AMPK/sirtuin-mediated energy sensing links dietary restriction to lifespan extension
Aging cell 2026
Open access · OA
Vitamin K2 Extends Lifespan by Alleviating Mitochondrial Stress via the JNK-1/SIR-2.1/DAF-16 Signaling Axis in Caenorhabditis elegans.
Food research international (Ottawa, Ont.) 2025
Citation only
Polysaccharide from Ganoderma atrum delay senescence and enhance stress resistance through modulating IIS and MAPK pathway in Caenorhabditis elegans.
Biochemical and Biophysical Research Communications 2015
Citation only
Oleanolic acid activates daf-16 to increase lifespan in Caenorhabditis elegans
Oxidative Medicine and Cellular Longevity 2019
Open access · CC-BY
Mitochondrial Oxidative Stress Impairs Energy Metabolism and Reduces Stress Resistance and Longevity of<i>C. elegans</i>
International Journal of Biological Macromolecules 2022
Citation only