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Curcumin supplementation increases longevity and antioxidant capacity in Caenorhabditis elegans

Curcumin is well known as a potent antioxidant and free radical scavenger and has great potential for anti-aging applications. In this study, we investigate the molecular mechanism of curcumin in prolonging the lifespan of C. elegans. Four concentrations of curcumin (10, 25, 50, and 100 µM) were adm...

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Autores principales: Xu, Jianing, Du, Pengyun, Liu, Xiaoyu, Xu, Xiao, Ge, Yuting, Zhang, Chenggang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10279890/
https://www.ncbi.nlm.nih.gov/pubmed/37346299
http://dx.doi.org/10.3389/fphar.2023.1195490
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author Xu, Jianing
Du, Pengyun
Liu, Xiaoyu
Xu, Xiao
Ge, Yuting
Zhang, Chenggang
author_facet Xu, Jianing
Du, Pengyun
Liu, Xiaoyu
Xu, Xiao
Ge, Yuting
Zhang, Chenggang
author_sort Xu, Jianing
collection PubMed
description Curcumin is well known as a potent antioxidant and free radical scavenger and has great potential for anti-aging applications. In this study, we investigate the molecular mechanism of curcumin in prolonging the lifespan of C. elegans. Four concentrations of curcumin (10, 25, 50, and 100 µM) were administered, and the optimal treatment concentration was determined by analyzing the nematode lifespan, physiology, and biochemistry. Additionally, RNA-seq and qRT-PCR were performed to explore the antioxidant effect of curcumin and its underlying mechanism. Results revealed that curcumin could significantly improve the survival capacity of C. elegans without influencing its growth. Curcumin was observed to significantly decrease the levels of reactive oxygen species (ROS) under extreme conditions such as heat stress and paraquat stress. In addition, curcumin increased the amount of nematode mitochondrial DNA (mtDNA) replication. RNA-seq results revealed that the underlying mechanism of curcumin in C. elegans is related to the mitogen-activated protein kinase (MAPK) pathway. qRT-PCR results confirmed that the expression of oxidative stress-related genes (sod-1, sod-2, sod-3, gst-4) was increased, and the expression of MAPK signaling pathway-related genes (sek-1, pmk-1, nsy-1) was significantly downregulated. Furthermore, the administration of curcumin extended the lifespan of nematodes, potentially through the enhancement of oxidative stress resistance and the downregulation of the MAPK signaling pathway. These findings improve our understanding of both lifespan extension and the potential mechanism of curcumin in C. elegans.
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spelling pubmed-102798902023-06-21 Curcumin supplementation increases longevity and antioxidant capacity in Caenorhabditis elegans Xu, Jianing Du, Pengyun Liu, Xiaoyu Xu, Xiao Ge, Yuting Zhang, Chenggang Front Pharmacol Pharmacology Curcumin is well known as a potent antioxidant and free radical scavenger and has great potential for anti-aging applications. In this study, we investigate the molecular mechanism of curcumin in prolonging the lifespan of C. elegans. Four concentrations of curcumin (10, 25, 50, and 100 µM) were administered, and the optimal treatment concentration was determined by analyzing the nematode lifespan, physiology, and biochemistry. Additionally, RNA-seq and qRT-PCR were performed to explore the antioxidant effect of curcumin and its underlying mechanism. Results revealed that curcumin could significantly improve the survival capacity of C. elegans without influencing its growth. Curcumin was observed to significantly decrease the levels of reactive oxygen species (ROS) under extreme conditions such as heat stress and paraquat stress. In addition, curcumin increased the amount of nematode mitochondrial DNA (mtDNA) replication. RNA-seq results revealed that the underlying mechanism of curcumin in C. elegans is related to the mitogen-activated protein kinase (MAPK) pathway. qRT-PCR results confirmed that the expression of oxidative stress-related genes (sod-1, sod-2, sod-3, gst-4) was increased, and the expression of MAPK signaling pathway-related genes (sek-1, pmk-1, nsy-1) was significantly downregulated. Furthermore, the administration of curcumin extended the lifespan of nematodes, potentially through the enhancement of oxidative stress resistance and the downregulation of the MAPK signaling pathway. These findings improve our understanding of both lifespan extension and the potential mechanism of curcumin in C. elegans. Frontiers Media S.A. 2023-06-06 /pmc/articles/PMC10279890/ /pubmed/37346299 http://dx.doi.org/10.3389/fphar.2023.1195490 Text en Copyright © 2023 Xu, Du, Liu, Xu, Ge and Zhang. 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
Xu, Jianing
Du, Pengyun
Liu, Xiaoyu
Xu, Xiao
Ge, Yuting
Zhang, Chenggang
Curcumin supplementation increases longevity and antioxidant capacity in Caenorhabditis elegans
title Curcumin supplementation increases longevity and antioxidant capacity in Caenorhabditis elegans
title_full Curcumin supplementation increases longevity and antioxidant capacity in Caenorhabditis elegans
title_fullStr Curcumin supplementation increases longevity and antioxidant capacity in Caenorhabditis elegans
title_full_unstemmed Curcumin supplementation increases longevity and antioxidant capacity in Caenorhabditis elegans
title_short Curcumin supplementation increases longevity and antioxidant capacity in Caenorhabditis elegans
title_sort curcumin supplementation increases longevity and antioxidant capacity in caenorhabditis elegans
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10279890/
https://www.ncbi.nlm.nih.gov/pubmed/37346299
http://dx.doi.org/10.3389/fphar.2023.1195490
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