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Effects of natural phytochemicals in Angelica sinensis (Danggui) on Nrf2‐mediated gene expression of phase II drug metabolizing enzymes and anti‐inflammation
Author(s) -
Saw Constance Lay Lay,
Wu Qing,
Su ZhengYuan,
Wang Hu,
Yang Yinhua,
Xu Xiaoting,
Huang Ying,
Khor Tin Oo,
Kong AhNg Tony
Publication year - 2013
Publication title -
biopharmaceutics and drug disposition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.419
H-Index - 58
eISSN - 1099-081X
pISSN - 0142-2782
DOI - 10.1002/bdd.1846
Subject(s) - sulforaphane , oxidative stress , chemistry , antioxidant , angelica sinensis , gene expression , pharmacology , luciferase , biochemistry , gene , biology , medicine , traditional chinese medicine , transfection , alternative medicine , pathology
ABSTRACT The root of Angelica sinensis (Oliv.) Diels (abbreviated as AS) (Danggui) has a long history in Asian herbal medicine. Recently, it was demonstrated that AS possesses anti‐cancer and anti‐oxidant activities. Because the transcription factor Nrf2 mediates the expression of many cellular anti‐oxidative stress genes, including genes that are involved in phase II drug metabolism and anti‐oxidative stress, this study sought to investigate whether pure compounds from AS or an AS extract could activate antioxidant response element (ARE)‐mediated gene expression and induce anti‐inflammatory activities. Z‐Ligustilide (Ligu), 3‐butylidenephthalide (Buty) and CO 2 supercritical fluid‐extracted lipophilic AS extract (SFE) were tested in HepG2‐C8 cells stabilized with ARE luciferase reporter gene. Ligu and Buty caused significant toxicity only at 100 μ m . All three samples induced ARE‐luciferase activity; however, SFE at 8.5 µg/ml induced ARE‐luciferase activity 2–3 fold more potently than did either of the pure compounds. SFE also significantly increased the endogenous mRNA of Nrf2 and the Nrf2 target anti‐oxidative gene NAD(P)H dehydrogenase, quinone 1 (NQO1). The protein expression of NQO1 was also significantly induced by SFE. In RAW 264.7 cells, SFE suppressed lipopolysaccharide (LPS)‐induced IL‐1β and TNF‐α expression about 2 fold stronger than sulforaphane, whereas both pure compounds and SFE suppressed inflammatory nitric oxide (NO) production. In summary, this study demonstrates that AS has anti‐inflammatory effects and activates the Nrf2 pathway, which protects against oxidative stress. Copyright © 2013 John Wiley & Sons, Ltd.