Astaxanthin attenuates UV‐irradiation aging process via activating JNK‐1/DAF‐16 in Caenorhabditis elegans

Author:

Lin Xiuping12,Shao Chang‐sheng1,Elsherbiny Shereen M.13,Huang Qing12ORCID

Affiliation:

1. CAS Key Laboratory of High Magnetic Field and Ion Beam Physical Biology, Anhui Key Laboratory of Environmental Toxicology and Pollution Control Technology, Institute of Intelligent Machine, Hefei Institutes of Physical Science Chinese Academy of Sciences Hefei China

2. Science Island Branch of Graduate School University of Science and Technology of China Hefei China

3. Physics Department, Faculty of Science Mansoura University Mansoura Egypt

Abstract

AbstractAstaxanthin (AST) is a xanthophyll carotenoid with strong oxidation resistance, which can effectively scavenge various free radicals and protect organisms from oxidative damage. AST is also known to have prominent anti‐aging effects, but the underlying mechanism of AST in anti‐radiation aging is largely unknown. In this work, we applied ultraviolet (UV) irradiation to accelerate the aging of Caenorhabditis elegans (C. elegans) and treated the nematodes with AST to explore whether and how AST could attenuate the radiation‐induced aging effect. Our results showed that AST improved the survival rate of C. elegans, reduced the aging biomarkers, and alleviated the mitochondrial dysfunction caused by the irradiation. Based on the transcriptome sequencing analysis, we identified that the key genes regulated by AST were involved in JNK‐MAPK and DAF‐16 longevity signaling pathways. Furthermore, we employed jnk‐1 and daf‐16 mutants and verified the role of the JNK‐1/DAF‐16 signaling pathway in the anti‐aging effect. As such, this study has not only demonstrated that AST can resist the aging process caused by UV‐irradiation but also revealed the anti‐aging mechanism of AST through JNK‐1/DAF‐16 activation in C. elegans.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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