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 32μM 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/EBPα, PPAR-γ, 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 (64μM initial concentration) added to the culture medium of 3T3-L1 cells was cleared within 6h. 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.
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