Gali-Muhtasib H U, Haddadin M J, Nazer M Z, Sodir N M, Maalouf S W
Department of Biology, American University of Beirut, Lebanon.
Med Oncol. 1998 Dec;15(4):262-9. doi: 10.1007/BF02787210.
2-benzoyl-3-phenylquinoxaline 1,4-dioxide (BPQ) and other substituted quinoxaline 1,4-dioxides (QdO) were tested for their ability to inhibit the stimulations of ornithine decarboxylase (ODC) enzyme activity and DNA synthesis, two biochemical markers linked to skin tumour promotion by ultraviolet B (UVB) radiation. Topical application of BPQ on the dorsal skin of hairless mice was found to inhibit in a dose-dependent manner UVB-induced ODC activity and DNA synthesis. When applied 20 min before UVB radiation, a dose of 17 mg BPQ applied in 0.4 ml of vehicle inhibited UVB-induced ODC activity and DNA synthesis by 95% and 85%, respectively. This inhibitory effect is dependent on the time of administration of BPQ relative to UVB radiation, with a generally greater inhibition observed when this compound is applied before rather than after UVB treatment. The inhibitory abilities of the other QdO on the ODC and DNA responses induced by UVB radiation greatly varied and appear to be dependent on the structure of the compounds and their metabolic activation in the skin following irradiation. The remarkable effectiveness of BPQ against the ODC and DNA markers of UVB promotion is also observed following multiple applications of this agent. These results suggest that QdO, in particular BPQ and certain derivatives of it, may be useful in protecting the skin against UVB-induced skin damage.
2-苯甲酰基-3-苯基喹喔啉-1,4-二氧化物(BPQ)及其他取代的喹喔啉-1,4-二氧化物(QdO),针对其抑制鸟氨酸脱羧酶(ODC)酶活性和DNA合成的能力进行了测试,这两种生化标志物与紫外线B(UVB)辐射引起的皮肤肿瘤促进作用相关。研究发现,将BPQ局部涂抹于无毛小鼠的背部皮肤,可呈剂量依赖性地抑制UVB诱导的ODC活性和DNA合成。在UVB辐射前20分钟应用时,0.4毫升赋形剂中所含17毫克BPQ的剂量分别抑制UVB诱导的ODC活性和DNA合成达95%和85%。这种抑制作用取决于BPQ相对于UVB辐射的给药时间,当该化合物在UVB处理之前而非之后应用时,通常观察到更大程度的抑制。其他QdO对UVB辐射诱导的ODC和DNA反应的抑制能力差异很大,似乎取决于化合物的结构及其在照射后皮肤中的代谢活化情况。在多次应用该药物后,也观察到BPQ对UVB促进作用的ODC和DNA标志物具有显著效果。这些结果表明,QdO,特别是BPQ及其某些衍生物,可能有助于保护皮肤免受UVB诱导的皮肤损伤。