Trigonelline Extends the Lifespan of C. Elegans and Delays the Progression of Age-Related Diseases by Activating AMPK, DAF-16, and HSF-1

被引:28
|
作者
Zeng, Wen-Yu [1 ]
Tan, Lin [2 ]
Han, Cong [1 ]
Zheng, Zhuo-Ya [2 ]
Wu, Gui-Sheng [2 ,3 ]
Luo, Huai-Rong [2 ,3 ]
Li, Su-Lian [1 ]
机构
[1] Southwest Med Univ, Affiliated Tradit Chinese Med Hosp, Luzhou 646000, Sichuan, Peoples R China
[2] Southwest Med Univ, Sch Pharm, Dept Pharmacol, Key Lab Aging & Regenerat Med, 319 Zhongshan Rd, Luzhou 646000, Sichuan, Peoples R China
[3] Cent Nervous Syst Drug Key Lab Sichuan Prov, Luzhou 646000, Sichuan, Peoples R China
关键词
TRANSCRIPTION FACTOR; INHIBITION; COMPONENTS; APOPTOSIS; RESPONSES; ACID;
D O I
10.1155/2021/7656834
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Trigonelline is the main alkaloid with bioactivity presented in fenugreek, which was used in traditional medicine in Asian countries for centuries. It is reported that trigonelline has anti-inflammatory, anti-oxidant, and anti-pathogenic effects. We are wondering whether trigonelline have anti-aging effect. We found that 50 mu M of trigonelline had the best anti-aging activity and could prolong the lifespan of Caenorhabditis elegans (C. elegans) by about 17.9%. Trigonelline can enhance the oxidative, heat, and pathogenic stress resistance of C. elegans. Trigonelline could also delay the development of neurodegenerative diseases, such as AD, PD, and HD, in models of C. elegans. Trigonelline could not prolong the lifespan of long-lived worms with loss-of-function mutations in genes regulating energy and nutrition, such as clk-1, isp-1, eat-2, and rsks-1. Trigonelline requires daf-16, hsf-1, and aak-2 to extend the lifespan of C. elegans. Trigonelline can also up-regulate the expression of daf-16 and hsf-1 targeted downstream genes, such as sod-3, gst-4, hsp-16.1, and hsp-12.6. Our results can be the basis for developing trigonelline-rich products with health benefits, as well as for further research on the pharmacological usage of trigonelline.
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页数:11
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