Lu Y P, Chang R L, Huang M T, Conney A H
Department of Chemical Biology and Pharmacognosy, College of Pharmacy, Rutgers, State University of New Jersey, Piscataway 08855-0789.
Carcinogenesis. 1993 Feb;14(2):293-7. doi: 10.1093/carcin/14.2.293.
Application of 5 nmol 12-O-tetradecanoylphorbol-13-acetate (TPA) to the skin of female CD-1 mice led to a rapid increase in the concentration of epidermal ornithine decarboxylase (ODC) mRNA from an undetectable level in control mice to a high maximum level at 4-5 h after TPA administration. The concentration of epidermal ODC mRNA then decreased rapidly during the next 5 h. The time course for TPA-induced increases in epidermal ODC enzyme activity paralleled very closely the time course for TPA-induced increases in ODC mRNA. Topical administration of 1, 3 or 10 mumol curcumin together with 5 nmol TPA inhibited by 66, 81 and 91% respectively TPA-induced increases in epidermal ODC enzyme activity measured 5 h later. In a parallel study, TPA-induced increases in the concentration of epidermal ODC mRNA was inhibited by 54, 85 and 82% respectively. Intraperitoneal injection of 10 or 30 mumol curcumin 1h before topical application of 5 nmol TPA inhibited TPA-induced increases in epidermal ODC enzyme activity by 75 or 89% respectively. In a parallel study, the induction of epidermal ODC mRNA was inhibited by 53 and 65% respectively. The results indicate that curcumin inhibits TPA-induced increases in epidermal ODC enzyme activity by inhibiting the synthesis and/or enhancing the breakdown of ODC mRNA.
将5纳摩尔的12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)涂抹于雌性CD - 1小鼠的皮肤上,导致表皮鸟氨酸脱羧酶(ODC)mRNA浓度迅速升高,从对照小鼠中无法检测到的水平升至TPA给药后4 - 5小时的最高水平。随后,表皮ODC mRNA浓度在接下来的5小时内迅速下降。TPA诱导表皮ODC酶活性增加的时间进程与TPA诱导ODC mRNA增加的时间进程非常紧密地平行。与5纳摩尔TPA一起局部施用1、3或10微摩尔姜黄素,分别在5小时后抑制TPA诱导的表皮ODC酶活性增加66%、81%和91%。在一项平行研究中,TPA诱导的表皮ODC mRNA浓度增加分别被抑制54%、85%和82%。在局部施用5纳摩尔TPA前1小时腹腔注射10或30微摩尔姜黄素,分别抑制TPA诱导表皮ODC酶活性增加75%或89%。在一项平行研究中,表皮ODC mRNA的诱导分别被抑制53%和65%。结果表明,姜黄素通过抑制ODC mRNA的合成和/或增强其降解来抑制TPA诱导的表皮ODC酶活性增加