Changes in the constituents and UV-photoprotective activity of Astragalus membranaceus caused by roasting
10.4163/jnh.2019.52.5.413
- Author:
Jeong Yong PARK
1
;
Ji Yeon LEE
;
Hyung Don KIM
;
Gwi Yeong JANG
;
Kyung Hye SEO
Author Information
1. Department of Herbal Crop Research, National Institute of Horticultural & Herbal Science, Eumsung, Chungbuk 27709, Korea. seokh@korea.kr
- Publication Type:Original Article
- Keywords:
Astragalus membranaceus;
UV-photoprotective activity;
antioxidant;
DNA damage
- MeSH:
Astragalus membranaceus;
Cell Survival;
Chromatography, Liquid;
Comet Assay;
DNA Damage;
Oxidative Stress;
Phenol;
Plants, Medicinal
- From:Journal of Nutrition and Health
2019;52(5):413-421
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: Astragalus membranaceus (AM) is an important traditional medicinal herb. Pharmacological research has indicated that AM has various physiological activities such as antioxidant, anti-inflammatory, immunoregulatory, anticancer, hypolipidemic, antihyperglycemic, and hepatoprotective activities. The bioactive substances responsible for the physiological activities in AM, including many antioxidant substances, change during the roasting process. This study investigated and compared the changes in the antioxidant constituents of AM caused by roasting. METHODS: DPPH (1,1-diphenyl-2-picryl hydrazyl) and ABTS⁺ (2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt) radical scavenging activities and their total phenolic content (TPC) were measured. High-performance liquid chromatography (HPLC) analysis was performed to confirm any changes in the isoflavonoids of roasted AM (R-AM),. The cell viability of UVB-induced HDF (Human dermal fibroblast) cells treated with AM and R-AM extracts was investigated. The comet assay was used to examine the inhibitory effects of R-AM extracts on DNA damage caused by oxidative stress. RESULTS: The DPPH and ABTS⁺ radical scavenging activities were 564.6±20.9 and 108.2±3.1 (IC₅₀ value) respectively, from the 2R-AM. The total phenol content was 47.80±1.40 mg GAE/g from the 1R-AM. The values of calycosin and formononetin, which are the known isoflavonoid constituents of AM, were 778.58±2.72 and 726.80±3.45 µg/g respectively, from the 2R-AM. Treatment of the HDF cells with R-AM (50 ~ 200 µg/mL) did not affect the cell viability. Furthermore, the R-AM extracts effectively protected against UVB-induced DNA damage. CONCLUSION: The findings of this study indicate that R-AM increases its isoflavonoid constituents and protects against UVB-induced DNA damage in HDF cells.
