3 '-Deoxyadenosine inhibits pre-adipocyte differentiation and biosynthesis of triacylglycerol in 3T3-L1 cells

Authors
Shin, Yong-KyuYe, Michael B.Kim, Sung-WonLee, Soo-ChanKim, Il-WoungKim, Su-NamYang, Hyun-OkKim, Si-Kwan
Issue Date
2014-01
Publisher
ELSEVIER SCIENCE BV
Citation
JOURNAL OF FUNCTIONAL FOODS, v.6, pp.331 - 338
Abstract
This study intended to develop anti-obesity compounds from natural sources. In our screening program for anti-obesity agents, a compound isolated from Cordyceps militaris was found to be a potent inhibitor of the differentiation of 3T3-L1 pre-adipocytes. The active ingredient of C. militaris was isolated from methanol extracts by chromatography, re-crystallized in water, and subsequently identified as 3'-deoxyadenosine, otherwise known as cordycepin. Cordycepin was a potent inhibitor of cellular differentiation and triacylglycerol (TAG) synthesis at a concentration of 32 mu M without any signs of cytotoxicity. However, the inhibitory action was attenuated by supplementation with adenosine. Western blot analysis revealed that cordycepin down-regulated the protein levels of C/EBP alpha, PPAR-gamma, and anti-leptin; these proteins are known to be associated with TAG synthesis. Cordycepin-induced decrease in protein expression was countered by the addition of adenosine. In vitro pharmacokinetic studies demonstrate that 95% of the cordycepin (64 mu M initial concentration) added to the culture medium of 3T3-L1 cells was cleared within 6 h. The metabolic rate of cordycepin in vitro was similar to that of adenosine, suggesting that cordycepin inhibits the differentiation of pre-adipocytes and blocks the synthesis of TAG in 3T3-L1 cells by interfering with adenosine metabolism. (C) 2014 Published by Elsevier Ltd.
Keywords
CORDYCEPS-SINENSIS; SCIENTIFIC REDISCOVERY; PPAR-GAMMA; MILITARIS; OBESITY; PREVALENCE; MEDICINE; RECEPTOR; WEIGHT; CORDYCEPS-SINENSIS; SCIENTIFIC REDISCOVERY; PPAR-GAMMA; MILITARIS; OBESITY; PREVALENCE; MEDICINE; RECEPTOR; WEIGHT; 3T3-L1 cells; Cordycepin; Differentiation; Triacylglycerol; Anti-obesity; In vitro pharmacokinetics
ISSN
1756-4646
URI
https://pubs.kist.re.kr/handle/201004/127280
DOI
10.1016/j.jff.2013.10.024
Appears in Collections:
KIST Article > 2014
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