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Lycium barbarum glycopetide prolong lifespan and alleviate Parkinson’s disease in Caenorhabditis elegans
INTRODUCTION: Lycium barbarum glycopeptide (LbGp) is the main bioactive compound extracted from the traditional Chinese medicine. L. barbarum berries and has been proven to have numerous health benefits, including antioxidative, anti-inflammatory, anticancer, and cytoprotective activities. However,...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10353607/ https://www.ncbi.nlm.nih.gov/pubmed/37469953 http://dx.doi.org/10.3389/fnagi.2023.1156265 |
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author | Zheng, Jingming Luo, Zhenhuan Chiu, Kin Li, Yimin Yang, Jing Zhou, Qinghua So, Kwok-Fai Wan, Qin-Li |
author_facet | Zheng, Jingming Luo, Zhenhuan Chiu, Kin Li, Yimin Yang, Jing Zhou, Qinghua So, Kwok-Fai Wan, Qin-Li |
author_sort | Zheng, Jingming |
collection | PubMed |
description | INTRODUCTION: Lycium barbarum glycopeptide (LbGp) is the main bioactive compound extracted from the traditional Chinese medicine. L. barbarum berries and has been proven to have numerous health benefits, including antioxidative, anti-inflammatory, anticancer, and cytoprotective activities. However, the antiaging effect of LbGp remains unknown. METHODS: The lifespan and body movement of C. elegans were used to evaluate the effect of LbGp on lifespan and health span. The thrashing assay was used to determine the role of LbGp in Parkinson’s disease. To investigate the mechanisms of LbGp-induced antiaging effects, we analyzed changes in lifespan, movement, and the expression of longevity-related genes in a series of worm mutants after LbGp treatment. RESULTS: We found that LbGp treatment prolonged the lifespan and health span of C. elegans. Mechanistically, we found that LbGp could activate the transcription factors DAF-16/FOXO, SKN-1/Nrf2, and HSF-1, as well as the nuclear receptor DAF-12, thereby upregulating longevity-related genes to achieve lifespan extension. In addition, we found that the lifespan extension induced by LbGp partially depends on mitochondrial function. Intriguingly, LbGp also ameliorated neurodegenerative diseases such as Parkinson’s disease in a DAF-16-, SKN-1-, and HSF-1-dependent manner. CONCLUSION: Our work suggests that LbGp might be a viable candidate for the treatment and prevention of aging and age-related diseases. |
format | Online Article Text |
id | pubmed-10353607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103536072023-07-19 Lycium barbarum glycopetide prolong lifespan and alleviate Parkinson’s disease in Caenorhabditis elegans Zheng, Jingming Luo, Zhenhuan Chiu, Kin Li, Yimin Yang, Jing Zhou, Qinghua So, Kwok-Fai Wan, Qin-Li Front Aging Neurosci Neuroscience INTRODUCTION: Lycium barbarum glycopeptide (LbGp) is the main bioactive compound extracted from the traditional Chinese medicine. L. barbarum berries and has been proven to have numerous health benefits, including antioxidative, anti-inflammatory, anticancer, and cytoprotective activities. However, the antiaging effect of LbGp remains unknown. METHODS: The lifespan and body movement of C. elegans were used to evaluate the effect of LbGp on lifespan and health span. The thrashing assay was used to determine the role of LbGp in Parkinson’s disease. To investigate the mechanisms of LbGp-induced antiaging effects, we analyzed changes in lifespan, movement, and the expression of longevity-related genes in a series of worm mutants after LbGp treatment. RESULTS: We found that LbGp treatment prolonged the lifespan and health span of C. elegans. Mechanistically, we found that LbGp could activate the transcription factors DAF-16/FOXO, SKN-1/Nrf2, and HSF-1, as well as the nuclear receptor DAF-12, thereby upregulating longevity-related genes to achieve lifespan extension. In addition, we found that the lifespan extension induced by LbGp partially depends on mitochondrial function. Intriguingly, LbGp also ameliorated neurodegenerative diseases such as Parkinson’s disease in a DAF-16-, SKN-1-, and HSF-1-dependent manner. CONCLUSION: Our work suggests that LbGp might be a viable candidate for the treatment and prevention of aging and age-related diseases. Frontiers Media S.A. 2023-07-04 /pmc/articles/PMC10353607/ /pubmed/37469953 http://dx.doi.org/10.3389/fnagi.2023.1156265 Text en Copyright © 2023 Zheng, Luo, Chiu, Li, Yang, Zhou, So and Wan. 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 | Neuroscience Zheng, Jingming Luo, Zhenhuan Chiu, Kin Li, Yimin Yang, Jing Zhou, Qinghua So, Kwok-Fai Wan, Qin-Li Lycium barbarum glycopetide prolong lifespan and alleviate Parkinson’s disease in Caenorhabditis elegans |
title | Lycium barbarum glycopetide prolong lifespan and alleviate Parkinson’s disease in Caenorhabditis elegans |
title_full | Lycium barbarum glycopetide prolong lifespan and alleviate Parkinson’s disease in Caenorhabditis elegans |
title_fullStr | Lycium barbarum glycopetide prolong lifespan and alleviate Parkinson’s disease in Caenorhabditis elegans |
title_full_unstemmed | Lycium barbarum glycopetide prolong lifespan and alleviate Parkinson’s disease in Caenorhabditis elegans |
title_short | Lycium barbarum glycopetide prolong lifespan and alleviate Parkinson’s disease in Caenorhabditis elegans |
title_sort | lycium barbarum glycopetide prolong lifespan and alleviate parkinson’s disease in caenorhabditis elegans |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10353607/ https://www.ncbi.nlm.nih.gov/pubmed/37469953 http://dx.doi.org/10.3389/fnagi.2023.1156265 |
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