Meet Inspiring Speakers and Experts at our 3000+ Global Conference Series Events with over 1000+ Conferences, 1000+ Symposiums
and 1000+ Workshops on Medical, Pharma, Engineering, Science, Technology and Business.

Explore and learn more about Conference Series : World's leading Event Organizer

Back

Hui-Hui Xiao

Hui-Hui Xiao

The Hong Kong Polytechnic University, PR China

Title: Lignans from Sambucus williamsii Hance exerts oestrogen-like effects in osteoblastic cells and its metabolites in rats

Biography

Biography: Hui-Hui Xiao

Abstract

Sambucus williamsii Hance, as a fork herbal medicine has been used in China on treatment of bone and joint diseases for thousands of years. Our previous studies clearly demonstrated that a fraction composed of 50% and 95% ethanol eluate from S. williamsii exerted protective effects on trabecular bone and cortical bone without side effects on uterus in ovariectomized mice and rats. The fraction is rich in lignans and 55 lignans were isolated and identified in this fraction. Among them, 44 lignans were characterized as bioactive components by in vitro activity screening. In the present study, PPD, a typical norlignan was selected for mechanism investigation involved in the anabolic effects of S. williamsii. The results showed that PPD exerted beneficial effects in osteoblasts and its effects were abolished by co-incubation with ICI 182,780 or U0126. It failed to bind to either ERα or ERβ at the concentration up to 10-6 M and did not activate estrogen response element (ERE)-ludiferase activities via ER. PPD induced the phosphorylation of ERK and ERα at serine 118. The data indicated that PPD exerts oestrogen-like actions in ostoblast-like cells via ligand-independent, ERE-independent and mitogen-activated protein (MAP) Kinase-mediated rapid nongenomic ER signalling pathway. In order to elucidate the real bioactive components in body, we further study the metabolites of DDA, a major norlignan in the bioactive fraction. In rats model, 14 metabolites were identified in the plasma, urine and feces administrated with DDA. The final metabolite was enterodiol. However, the metabolic pathway was still in study.

Speaker Presentations

Speaker PPTs Click Here