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Isolation of Saponins with the Inhibitory Effect on Nitric Oxide, Prostaglandin E2 and Tumor Necrosis Factor-α Production from Pleurospermum kamtschaticum

Authors
 Hyun-Ju Jung  ;  Sei-Gun Kim  ;  Jung-Hwan Nam  ;  Kwang-Kyun Park  ;  Won-Yun Chung  ;  Won-Bae Kim  ;  Kyung-Tae Lee  ;  Jong-Heon Won  ;  Jong-Won Choi  ;  Hee-Juhn Park 
Citation
 BIOLOGICAL & PHARMACEUTICAL BULLETIN, Vol.28(9) : 1668-1671, 2005 
Journal Title
BIOLOGICAL & PHARMACEUTICAL BULLETIN
ISSN
 0918-6158 
Issue Date
2005
MeSH
Anti-Inflammatory Agents, Non-Steroidal/isolation & purification* ; Anti-Inflammatory Agents, Non-Steroidal/pharmacology* ; Apiaceae/chemistry* ; Cell Line ; Cell Survival/drug effects ; Dinoprostone/antagonists & inhibitors* ; Humans ; Lipopolysaccharides/antagonists & inhibitors ; Lipopolysaccharides/toxicity ; Macrophages/drug effects ; Macrophages/metabolism ; Nitric Oxide/antagonists & inhibitors* ; Plant Extracts/pharmacology ; Prostaglandin Antagonists* ; Sapogenins/isolation & purification ; Sapogenins/pharmacology ; Saponins/isolation & purification* ; Saponins/pharmacology* ; Tetrazolium Salts ; Thiazoles ; Tumor Necrosis Factor-alpha/antagonists & inhibitors* ; Tumor Necrosis Factor-alpha/biosynthesis*
Keywords
Pleurospermum kamtschaticum ; Umbelliferae ; saponin ; nitric oxide ; prostaglandin E2 ; tumor necrosis factor-α
Abstract
As an attempt to search for bioactive natural products exerting antiinflammatory activity, we have isolated two saponins were isolated from the aerial portion of Pleurospermum kamtschaticum (Umbelliferae) by nitrite assay activity-directed chromatographic fractionation. They were identified as saikogenin F 3-O-{β-D-glucopyranosyl-(1→2)-[β-D-glucopyranosyl-(1→3)]-β-D-fucopyranoside} (buddlejasaponin IV, 1) and 3β,16β,23,28-tetrahydroxy-11α-methoxyolean-12-ene 3-O-{β-D-glucopyranosyl(1→2)-[β-D-glucopyranosyl(1→3)]-β-D-fucopyranoside} (buddlejasaponin IVa, 2). Compound 1 significantly inhibited nitric oxide (NO) production, and it also significantly decreased prostaglandin E2 (PGE2) and tumor necrosis factor-α (TNF-α) release in the lipopolysaccharide (LPS)-activated macrophage Raw 264.7 cells whereas compound 2 was much less active. Saikogenin A (3) and –H (4) were obtained by hydrolyzing 1 and 2. Although these sapogenin showed strong NO inhibition, these effects were caused by the cytotoxic effect on Raw 264.7 cells. These results supported the notion that buddlejasaponin IV is a major inhibitors of NO, PGE2 and TNF-α production in P. kamtschaticum.
Files in This Item:
T200501196.pdf Download
DOI
10.1248/bpb.28.1668
Appears in Collections:
2. College of Dentistry (치과대학) > Dept. of Oral Biology (구강생물학교실) > 1. Journal Papers
Yonsei Authors
Park, Kwang Kyun(박광균)
Chung, Won Yoon(정원윤) ORCID logo https://orcid.org/0000-0001-8428-9005
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/151366
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