Raunio H, Pelkonen O
J Invest Dermatol. 1982 Oct;79(4):246-9. doi: 10.1111/1523-1747.ep12500071.
Changes in the activities of ornithine decarboxylase (ODC) and aryl hydrocarbon hydroxylase (AHH) were investigated in rat epidermis after wounding the skin and application of 7,12-dimethylbenz(a)anthracene (DMBA), 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), and several enzyme inhibitors. Wounding of the skin by vigorous shaving led to a marked induction of ODC activity with a peak at 6 hr. Topical application of a single dose of tetradecanoylphorbol-13-acetate to wounded skin did not affect the activities of ODC and AHH. Application of single large dose (2.5 mg) of DMBA increased AHH activity 7-fold without affecting ODC activity. DL-alpha-difluoromethyl ornithine, a specific irreversible inhibitor of ODC, almost completely abolished ODC activity but did not inhibit DMBA- or TCDD-induced AHH activity. Several potential modifiers, including retinoic acid, indomethacin, 1,3-diamino-2-propranol, alpha-naphthoflavone, and SKF 525 A had unequal effects on ODC and AHH activities. These data indicate that ODC and AHH induction processes in the epidermis are independent biochemical events that are not causally related.
在对大鼠皮肤进行创伤以及涂抹7,12 - 二甲基苯并(a)蒽(DMBA)、2,3,7,8 - 四氯二苯并 - p - 二恶英(TCDD)和几种酶抑制剂后,研究了鸟氨酸脱羧酶(ODC)和芳烃羟化酶(AHH)在大鼠表皮中的活性变化。用力剃毛对皮肤造成创伤后,ODC活性显著诱导,在6小时达到峰值。对创伤皮肤局部涂抹单剂量的十四酰佛波醇 - 13 - 乙酸酯并不影响ODC和AHH的活性。涂抹单一大剂量(2.5毫克)的DMBA可使AHH活性增加7倍,而不影响ODC活性。DL-α-二氟甲基鸟氨酸是ODC的一种特异性不可逆抑制剂,几乎完全消除了ODC活性,但不抑制DMBA或TCDD诱导的AHH活性。几种潜在的调节剂,包括视黄酸、吲哚美辛、1,3 - 二氨基 - 2 - 丙醇、α-萘黄酮和SKF 525 A对ODC和AHH活性有不同的影响。这些数据表明,表皮中ODC和AHH的诱导过程是独立的生化事件,没有因果关系。