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Preparative isolation of sargachromanol E from Sargassum siliquastrum by centrifugal partition chromatography and its anti-inflammatory activity

Authors
Lee, Ji-HyeokKo, Ju-YoungSamarakoon, KalpaOh, Jae-YoungHeo, Soo-JinKim, Chul-YoungNah, Jae-WoonJang, Mi-KyeongLee, Jung-SuckJeon, You-Jin
Issue Date
Dec-2013
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
Centrifugal partition chromatography; Sargachromanol E; Sargassum siliquastrum; Antiinflammatory activity; MAPK pathway
Citation
FOOD AND CHEMICAL TOXICOLOGY, v.62, pp.54 - 60
Indexed
SCIE
SCOPUS
Journal Title
FOOD AND CHEMICAL TOXICOLOGY
Volume
62
Start Page
54
End Page
60
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/26289
DOI
10.1016/j.fct.2013.08.010
ISSN
0278-6915
Abstract
Centrifugal partition chromatography (CPC) can be used to isolate various bioactive compounds from natural materials by one-step. We confirmed antioxidative compounds existed in chloroform (CHCl3) fraction of Sargassum siliquastrum using online-HPLC. Fractions (A, B, C, D and E) were separated from the CHCl3 fraction by preparative CPC (n-hexane:ethyl acetate:methanol:water, 5:5:7:3, v/v). In this study, we proved that the isolated compounds exhibit anti-inflammatory activities using lipopolysaccharide (LPS) stimulated RAW 264.7 macrophages. The fraction A which exhibited the strongest inhibitory effect on nitric oxide (NO) production level, was confirmed as sargachromanol E by LC-MS-ESI, H-1 NMR and C-13 NMR data. The sargachromanol E significantly reduced the inflammatory response in LPS induced macrophages, decreasing LPS-induced transcription factor of pro-inflammatory cyclooxygenase-2, NO synthase, phosphate P38, phosphate ERK1/2, LPS-stimulated tumor-necrosis factor alpha, interleukin-1 beta and prostaglandin E2 release. In conclusion, it was suggested that sargachromanol E inhibited inflammation in LPS induced RAW 264.7 cells via MAPK pathway. (C) 2013 Elsevier Ltd. All rights reserved.
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