Kelly G E, Sheil A G, Wass J, Zbroja R A
Br J Dermatol. 1986 Feb;114(2):197-208. doi: 10.1111/j.1365-2133.1986.tb02798.x.
The effects of immunosuppressive drugs on epidermal cell mitotic activity and the proliferative response of epidermis following ultraviolet radiation (UVR) were tested. Hairless (Skh-hr 1) mice were treated with immunosuppressive drugs at equivalent clinical doses with or without concomitant UVR (290-400 nm). Epidermal parameters measured were mitotic index (Im), rate of entry into mitosis (Fm), flash labelling index (FLI), rate of entry into DNA synthesis (Fs) and DNA content (flow cytometric analysis). In non-irradiated skin, prednisolone therapy depressed both mitotic activity and DNA synthesis; azathioprine and cyclosporin A had no effect; cyclophosphamide therapy increased the Fm and FLI values. Following repeated doses of UVR, there were enhanced mitotic activity and DNA synthesis in epidermis. Prednisolone therapy moderately depressed both proliferative responses; cyclophosphamide enhanced mitotic activity; azathioprine and cyclosporin A had no effect on these responses. The significance of these findings in relation to potential for increased susceptibility of skin to UV-induced carcinogenesis is discussed.
测试了免疫抑制药物对表皮细胞有丝分裂活性以及紫外线辐射(UVR)后表皮增殖反应的影响。将无毛(Skh-hr 1)小鼠用等效临床剂量的免疫抑制药物进行处理,同时或不同时给予UVR(290 - 400 nm)。所测量的表皮参数有有丝分裂指数(Im)、进入有丝分裂的速率(Fm)、闪光标记指数(FLI)、进入DNA合成的速率(Fs)以及DNA含量(流式细胞术分析)。在未照射的皮肤中,泼尼松龙治疗降低了有丝分裂活性和DNA合成;硫唑嘌呤和环孢素A无影响;环磷酰胺治疗增加了Fm和FLI值。在重复给予UVR后,表皮中有丝分裂活性和DNA合成增强。泼尼松龙治疗适度抑制了两种增殖反应;环磷酰胺增强了有丝分裂活性;硫唑嘌呤和环孢素A对这些反应无影响。讨论了这些发现对于皮肤对紫外线诱导致癌易感性增加可能性的意义。