Lee Seung Ho, Son Min Jung, Ju Hye Kyung, Lin Chang Xiu, Moon Tae Chul, Choi Han-Gon, Son Jong Keun, Chang Hyeun Wook
College of Pharmacy, Yeungnam University, Gyongsan, Japan.
Biol Pharm Bull. 2004 Jun;27(6):786-8. doi: 10.1248/bpb.27.786.
Deoxypodophyllotoxin (Anthricin) is a medicinal herbal product isolated from Anthriscus sylvestris HOFFM. that inhibits cyclooxygenase-2 (COX-2) and COX-1-dependent phases of prostaglandin D(2) (PGD(2)) generation in bone marrow-derived mast cells (BMMC) in a concentration-dependent manner with IC(50) values of 1.89 microM and 65.3 microM, respectively. This study also found that this compound inhibited COX-1 and 2-dependent conversion of the exogenous arachidonic acid to PGD(2) in a dose-dependent manner with an IC(50) values of 0.01 microM and 12.1 microM, respectively using a COX enzyme assay kit. However, this compound did not inhibit COX-2 protein expression up to a concentration of 30 microM in the BMMC, indicating that deoxypodophyllotoxin directly inhibits COX-2 activity. Furthermore, this compound consistently inhibited the production of leukotriene C(4) (LTC(4)) in a dose dependent manner, with an IC(50) value of 0.37 microM. These results demonstrate that deoxypodophyllotoxin has a dual cyclooxygenase-2 selective/5-lipoxygenase inhibitory activity, and therefore this compound might provide a basis for novel anti-inflammatory drugs.
脱氧鬼臼毒素(Anthricin)是一种从欧洲峨参(Anthriscus sylvestris HOFFM.)中分离得到的药用草药产品,它能以浓度依赖的方式抑制骨髓来源肥大细胞(BMMC)中前列腺素D2(PGD2)生成的环氧合酶-2(COX-2)和COX-1依赖阶段,其IC50值分别为1.89微摩尔和65.3微摩尔。本研究还发现,使用COX酶检测试剂盒,该化合物能以剂量依赖的方式抑制外源性花生四烯酸向PGD2的COX-1和COX-2依赖性转化,其IC50值分别为0.01微摩尔和12.1微摩尔。然而,在BMMC中,该化合物在浓度高达30微摩尔时并未抑制COX-2蛋白表达,这表明脱氧鬼臼毒素直接抑制COX-2活性。此外,该化合物能持续以剂量依赖的方式抑制白三烯C4(LTC4)的产生,IC50值为0.37微摩尔。这些结果表明脱氧鬼臼毒素具有双重环氧合酶-2选择性/5-脂氧合酶抑制活性,因此该化合物可能为新型抗炎药物提供基础。