Kim Sue Ok, Chun Kyung-Soo, Kundu Joydeb Kumar, Surh Young-Joon
College of Pharmacy, Seoul National University, Seoul 151-742, South Korea.
Biofactors. 2004;21(1-4):27-31. doi: 10.1002/biof.552210107.
[6]-Gingerol, a major pungent ingredient of ginger (Zingiber officinale Roscoe, Zingiberaceae), has a wide array of pharmacologic effects. Previous studies have demonstrated that [6]-gingerol inhibits mouse skin tumor promotion and anchorage-independent growth of cultured mouse epidermal cells stimulated with epidermal growth factor. Cyclooxygenase-2 (COX-2), a key enzyme in the prostaglandin biosynthesis, has been recognized as a molecular target for many anti-inflammatory as well as chemopreventive agents. Topical application of [6]-gingerol inhibited phorbol 12-myristate 13-acetate -induced COX-2 expression. One of the essential transcription factors responsible for COX-2 induction is NF-kappaB. [6]-Gingerol suppressed NF-kappaB DNA binding activity in mouse skin. In addition, [6]-gingerol inhibited the phoshorylation of p38 mitogen-activated protein kinase which may account for its inactivation of NF-kappaB and suppression of COX-2 expression.
[6]-姜辣素是姜(姜科植物姜Zingiber officinale Roscoe)的主要辛辣成分,具有广泛的药理作用。先前的研究表明,[6]-姜辣素可抑制小鼠皮肤肿瘤的促进作用以及表皮生长因子刺激的培养小鼠表皮细胞的非贴壁依赖性生长。环氧化酶-2(COX-2)是前列腺素生物合成中的关键酶,已被认为是许多抗炎和化学预防剂的分子靶点。局部应用[6]-姜辣素可抑制佛波酯12-肉豆蔻酸酯13-乙酸酯诱导的COX-2表达。负责COX-2诱导的重要转录因子之一是核因子κB(NF-κB)。[6]-姜辣素可抑制小鼠皮肤中NF-κB的DNA结合活性。此外,[6]-姜辣素可抑制p38丝裂原活化蛋白激酶的磷酸化,这可能是其使NF-κB失活并抑制COX-2表达的原因。