Abstract

The methanolic extract from the leaves of Laurus nobilis (bay leaf, laurel) was found to inhibit nitric oxide (NO) production in lipopolysaccharide (LPS)-activated mouse peritoneal macrophages. Through bioassay-guided separation, fourteen known sesquiterpenes were isolated from the active fraction and were examined for ability to inhibit the NO production. Seven sesquiterpene lactones (costunolide, dehydrocostus lactone, eremanthine, zaluzanin C, magnolialide, santamarine and spirafolide) potently inhibited LPS-induced NO production (IC 50 = 1.2~3.8 μM). Other sesquiterpene constituents also showed the inhibitory activity (IC 50 >= 21 μM), but their inhibitory activities were less than those of sesquiterpene lactones. α-Methylene-γ-butyrolactone also showed inhibitory activity (IC 50 = 9.6 μM), while mokko lactone and watsonol A etc., reductants of the α-methylene-γ-butyrolactone moiety by NaBH 4 or DIBAL and a 2-mercaptoethanol adduct of dehydrocostus lactone showed little activity (IC 50 >= 18 μM). These results indicated that the α-methylene-γ-butyrolactone moiety is important for the activity. Furthermore, costunolide and dehydrocostus lactone inhibited inducible nitric oxide synthase (iNOS) induction in accordance with induction of heat shock protein 72 (HSP 72). These results suggested that, as one of their mechanisms of action, sesquiterpene lactones induce HSP 72 thereby preventing nuclear factor-κB activation followed by iNOS induction.

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