期刊
PROCESS BIOCHEMISTRY
卷 47, 期 7, 页码 1073-1078出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.procbio.2012.03.011
关键词
Salicornia herbacea; Quercetin 3-O-beta-D-glucopyranoside; Anti-adipogenic differentiation
资金
- National Fisheries Research and Development Institute [RP-12-BT-21]
- Ministry of Land, Transport and Maritime Affairs (MLTM)
In the present study, the bioactivity-monitored isolation of flavonoid glucopyranosides from the saltmarsh plant Salicornia herbacea was performed, and their effects on adipogenic differentiation were evaluated in 3T3-L1 adipocytes. Among the solvent-partitioned fractions from S. herbacea, the 85% aq. MeOH and n-BuOH fractions effectively reduced the levels of triglyceride accumulation, glucose consumption and adipogenic transcription factor peroxisome proliferator-activated receptor-gamma (PPAR gamma) expression. Further purification of the n-BuOH fraction led to the isolation of two flavonoid glucopyranosides. isorhamnetin 3-O-beta-D-glucopyranoside (A) and quercetin 3-O-beta-D-glucopyranoside (B), as the active principles. The presence of glucopyranosides A and B in adipocyte cells effectively suppressed adipogenic differentiation. Comparative analysis indicated that adipogenic differentiation was dramatically attenuated in the presence of glucopyranoside B rather than glucopyranoside A. The anti-adipogenic activity of glucopyranosides B was confirmed by down-regulation of sterol regulatory element-binding protein 1 (SREBP1), CCAAT/enhancer-binding proteins (C/EBP alpha), PPAR gamma and the adipocyte-specific proteins. Moreover, the specific mechanism mediating the effects of glucopyranosides B was confirmed by activation of AMP-activated protein kinase (AMPK). Findings from this study should underscore the nutraceutical value of S. herbacea-derived glucopyranosides as potent anti-obesity agents via alleviation of lipid accumulation. (c) 2012 Elsevier Ltd. All rights reserved.
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