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黄连素通过多靶点协同抗氧化作用延长寿命。

Berberine Extends Lifespan in Through Multi-Target Synergistic Antioxidant Effects.

作者信息

Bei Yingshuo, Wang Ting, Guan Shuwen

机构信息

School of Life Sciences, Jilin University, Changchun 130012, China.

出版信息

Antioxidants (Basel). 2025 Apr 9;14(4):450. doi: 10.3390/antiox14040450.

DOI:10.3390/antiox14040450
PMID:40338239
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12024168/
Abstract

Aging is a process of gradual functional decline in complex physiological systems and is closely related to the occurrence of various diseases. Berberine, a bioactive alkaloid derived from (Huanglian), has emerged as a promising candidate for anti-aging interventions. This study comprehensively investigated the lifespan-extending effects and molecular mechanisms of berberine in through integrated approaches including lifespan assays, locomotor activity analysis, oxidative stress challenges, and transcriptomic profiling. Furthermore, genetic models of mutant and transgenic worms were employed to delineate their interactions with the insulin/IGF-1 signaling (IIS) pathway. Our results demonstrate that berberine extended the mean lifespan of wild-type worms by 27%. By activating transcription factors such as DAF-16/FOXO, HSF-1, and SKN-1/NRF2, berberine upregulated antioxidant enzyme expression, reduced lipofuscin accumulation, and improved stress resistance. Transcriptomic analysis revealed significant changes in lipid metabolism-related genes, particularly in pathways involving fatty acid synthesis, degradation, and sphingolipid metabolism. These findings establish that berberine exerts multi-target anti-aging effects through coordinated activation of stress-responsive pathways and metabolic optimization, providing mechanistic insights for developing natural product-based geroprotective strategies.

摘要

衰老乃是复杂生理系统中功能逐渐衰退的过程,且与多种疾病的发生密切相关。黄连素是一种从(黄连)中提取的生物活性生物碱,已成为抗衰老干预措施颇具前景的候选物。本研究通过包括寿命测定、运动活性分析、氧化应激挑战和转录组分析等综合方法,全面探究了黄连素在[具体生物]中的延寿作用及其分子机制。此外,利用突变和转基因蠕虫的遗传模型来描绘它们与胰岛素/IGF-1信号(IIS)通路的相互作用。我们的结果表明,黄连素使野生型蠕虫的平均寿命延长了27%。通过激活诸如DAF-16/FOXO、HSF-1和SKN-1/NRF2等转录因子,黄连素上调了抗氧化酶的表达,减少了脂褐素的积累,并提高了抗应激能力。转录组分析揭示了脂质代谢相关基因的显著变化,特别是在涉及脂肪酸合成、降解和鞘脂代谢的途径中。这些发现证实,黄连素通过协同激活应激反应通路和优化代谢发挥多靶点抗衰老作用,为开发基于天然产物的老年保护策略提供了机制性见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3806/12024168/7a01292353b7/antioxidants-14-00450-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3806/12024168/b5e96c9dc5d6/antioxidants-14-00450-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3806/12024168/d8b9100f7ef5/antioxidants-14-00450-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3806/12024168/2274ca64922c/antioxidants-14-00450-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3806/12024168/51f23a2e4a5e/antioxidants-14-00450-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3806/12024168/27d5e5783aaa/antioxidants-14-00450-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3806/12024168/7a01292353b7/antioxidants-14-00450-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3806/12024168/b5e96c9dc5d6/antioxidants-14-00450-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3806/12024168/04d545f2a7aa/antioxidants-14-00450-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3806/12024168/b4c3c3b82ddc/antioxidants-14-00450-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3806/12024168/1a948007f1a9/antioxidants-14-00450-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3806/12024168/d8b9100f7ef5/antioxidants-14-00450-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3806/12024168/2274ca64922c/antioxidants-14-00450-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3806/12024168/51f23a2e4a5e/antioxidants-14-00450-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3806/12024168/27d5e5783aaa/antioxidants-14-00450-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3806/12024168/7a01292353b7/antioxidants-14-00450-g009.jpg

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本文引用的文献

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