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Abstract Title:

Sesamin and sesamolin reduce amyloid-β toxicity in a transgenic Caenorhabditis elegans.

Abstract Source:

Biomed Pharmacother. 2018 Aug 14 ;107:656-664. Epub 2018 Aug 14. PMID: 30118882

Abstract Author(s):

Roongpetch Keowkase, Natthawut Shoomarom, Worawee Bunargin, Worapan Sitthithaworn, Natthida Weerapreeyakul

Article Affiliation:

Roongpetch Keowkase

Abstract:

Alzheimer's disease (AD) is a devastating neurodegenerative disease characterized byβ-amyloid (Aβ) plaques in the brain. At the present, there is no approved drug with a proven disease-modifying effect. Sesame seed (Sesame indicum) has long been known as a healthy food in Southeast Asian countries. Sesame lignans obtained from sesame seed possess antioxidant property that exhibita variety of beneficial effects in various models. The objective of this study was to investigate the protective effects of sesame lignans including sesamin, sesamolin, and sesamol against Aβ toxicity in Caenorhabditis elegans (C. elegans) model of Aβ toxicity and to address whether these sesamelignans have a positive effect on lifespan extension. A transgenic C. elegans expressing human Aβ was used to investigate protective effects of sesame lignans against Aβ toxicity. Sesamin and sesamolin significantly alleviated Aβ-induced paralysis. The real-time PCR revealed that both sesamin andsesamolin did not affect the expression of Aβ transgene. However, we found that only sesamin inhibited Aβ oligomerization. These findings demonstrated that, among three sesame lignans tested, sesamin protected against Aβ toxicity by reducing toxic Aβ oligomers. Sesamin and sesamolin also significantly improved Aβ-induced defect in chemotaxis behavior and reversed the defect to normal. Moreover, sesamin prolonged median and mean lifespan of the wild type worm. On the other hand, sesamolin and sesamol failed to extend lifespan. These results offer valuable evidence for the future use of sesamin in the development of agents for the treatment of AD. It is also worth investigating the structure-activity relationship of lignan-related structures and their anti-Aβ toxicity activities in the future.

Study Type : Animal Study

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Sayer Ji
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