Secoisolariciresinol Diglucoside Delays the Progression of Aging-Related Diseases and Extends the Lifespan ofCaenorhabditis elegansvia DAF-16 and HSF-1

Author:

Lu Min1,Tan Lin1,Zhou Xiao-Gang1,Yang Zhong-Lin1,Zhu Qing1,Chen Jian-Ning1,Luo Huai-Rong123ORCID,Wu Gui-Sheng12ORCID

Affiliation:

1. Key Laboratory for Aging and Regenerative Medicine, Department of Pharmacology School of Pharmacy, Southwest Medical University, Luzhou, Sichuan 646000, China

2. Key Laboratory of Medical Electrophysiology, Ministry of Education, Institute of Cardiovascular Research of Southwest Medical University, Luzhou, Sichuan 646000, China

3. Central Nervous System Drug Key Laboratory of Sichuan Province, Luzhou, Sichuan 646000, China

Abstract

Secoisolariciresinol diglucoside (SDG) is a phytoestrogen and rich in food flaxseed, sunflower seeds, and sesame seeds. Among the beneficial pharmacological activities of SDG on health, many are age related, such as anticancer, antidiabetes, antioxidant, and neuroprotective effects. Thus, we investigated if SDG had an effect on antiaging inCaenorhabditis elegans(C. elegans). Our results showed that SDG could extend the lifespan ofC. elegansby up to 22.0%, delay age-related decline of body movement, reduce the lethality of heat and oxidative stress, alleviate dopamine neurodegeneration induced by 6-hydroxydopamine (6-OHDA), and decrease the toxicity of Aβprotein inC. elegans. SDG could increase the expression of the downstream genes of DAF-16, DAF-12, NHR-80, and HSF-1 at mRNA level. SDG could not extend the lifespan of mutants from genesdaf-16,hsf-1,nhr-80,daf-12,glp-1,eat-2, andaak-2. The above results suggested that SDG might enhance the stress resistance, delay the progression of aging-related diseases, and extend the lifespan ofC. elegansvia DAF-16 and HSF-1.

Funder

Southwest Medical University

Publisher

Hindawi Limited

Subject

Cell Biology,Aging,General Medicine,Biochemistry

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