ESR Study on the Structure and Hydroxyl Radical-Scavenging Activity Relationships of Ginsenosides Isolated from Panax ginseng C. A. MEYER

Autor: Hyun Young Kim, Noriko Yamabe, Jeong Hill Park, Ki Sung Kang, Takako Yokozawa
Rok vydání: 2007
Předmět:
Zdroj: Biological and Pharmaceutical Bulletin. 30:917-921
ISSN: 1347-5215
0918-6158
DOI: 10.1248/bpb.30.917
Popis: Ginsenosides have been regarded as the main active components of Panax ginseng C. A. MEYER, and the an- tioxidant activity of ginsenosides in vivo is well described. However, there has been virtually no report describing the direct free radical-scavenging activities of ginsenosides through the long history of ginseng research. The hy- droxyl radical ( · OH)-scavenging activity test using an electron spin resonance spectrometer (ESR) is suggested to be the most appropriate to measure the antioxidant activities of ginsenosides. Therefore, we investigated the · OH-scavenging and ferrous metal ion-chelating activities of several ginsenosides of Panax ginseng using ESR for the identification of active ginsenosides and its structure and activity relationships. As a result, 20(S)-Rg3 showed the strongest activity, and the next were in the decreasing order of Rb 1 , Rg 1 , Rc, Rb 2 , and Rd when dissolved with water. The · OH-scavenging activities of ginsenosides were related to the ferrous metal ion-chelating activities of their aglycone, 20(S)-protopanaxadiol. In addition, the ferrous metal ion-chelating activities of ginsenosides were thought to be influenced by their types of hydrophilic sugar moieties.
Databáze: OpenAIRE