Back to Search Start Over

Effects of vitexin-2″- O-rhamnoside and vitexin-4″- O-glucoside on growth and oxidative stress-induced cell apoptosis of human adipose-derived stem cells.

Authors :
Wei, Wenjuan
Ying, Xixiang
Zhang, Wenjie
Chen, Yinghui
Leng, Aijing
Jiang, Chen
Liu, Jing
Source :
Journal of Pharmacy & Pharmacology; Jul2014, Vol. 66 Issue 7, p988-997, 10p
Publication Year :
2014

Abstract

Objectives Vitexin-2″- O-rhamnoside ( VOR) and vitexin-4″- O-glucoside ( VOG) are the two main flavonoid glycosides of the leaves of C ratagus pinnatifida Bge. var. major N. E. Br. that has been widely used for the treatment of cardiovascular system diseases. In this study, we simultaneously investigated the influence of VOR and VOG on human adipose-derived stem cells (h ADSCs) injury induced by hydrogen peroxide ( H<subscript>2</subscript>O<subscript>2</subscript>) to further characterize their anti-oxidative and anti-apoptotic activity. Methods h ADSCs were isolated, cultured in vitro and pretreated with 62.5 μ m VOR or 120 μ m VOG for 24 h and then exposed to 500 μ m H<subscript>2</subscript>O<subscript>2</subscript> for an additional 4 h. Key findings Pretreatment of h ADSCs with VOR and VOG was demonstrated to significantly ameliorate the toxicity and apoptosis effects, such as morphological distortion, nuclear condensation, decreased intracellular caspase-3 activity and percentage of cells in apoptosis/necrosis by using morphological assay, immunocytochemistry and flow cytometric evaluation. In addition, VOR and VOG caused no cytotoxic effect on hADSCs at concentrations up to 250 and 480 μ m, respectively. Conclusions Our results indicated that both VOR and VOG contribute to the protection against H<subscript>2</subscript>O<subscript>2</subscript>-mediated oxidative stress damage and could be safely used for a wide range of concentrations. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00223573
Volume :
66
Issue :
7
Database :
Complementary Index
Journal :
Journal of Pharmacy & Pharmacology
Publication Type :
Academic Journal
Accession number :
96443587
Full Text :
https://doi.org/10.1111/jphp.12225