Peters R F, White A M
Br J Dermatol. 1978 Mar;98(3):301-14. doi: 10.1111/j.1365-2133.1978.tb06157.x.
Sequential changes in skin metabolism have been studied in a model system of epidermal hyperplasia and hyperkeratinization induced by the application of n-hexadecane to shaved rat skin. The epidermal accumulation of glycogen typical of the hyperplastic response has been correlated with an increase in glycogenesis and a decrease in glycogenolysis. DNA synthesis was increased by 6 h after the start of hexadecane treatment and reached a maximum after one day. The concentration of skin cyclic AMP fell immediately after hexadecane application and subsequently rose to give a prolonged increase. Use of the combined topical application of hexadecane and the anti-inflammatory drugs triamcinolone acetonide, hydrocortisone and indomethacin showed that the hexadecane-induced changes in DNA synthesis and glycogen metabolism were linked to the initial fall in cyclic AMP concentration. The significance of the biphasic change in cyclic AMP levels is discussed as a possible system of control for the development and maintenance of hyperplasia.
在将正十六烷涂抹于剃毛大鼠皮肤所诱导的表皮增生和角化过度的模型系统中,对皮肤新陈代谢的顺序变化进行了研究。增生反应典型的表皮糖原积累与糖原生成增加和糖原分解减少相关。正十六烷处理开始后6小时,DNA合成增加,并在一天后达到最大值。涂抹正十六烷后,皮肤环磷酸腺苷(cAMP)浓度立即下降,随后上升并持续增加。联合局部应用正十六烷和抗炎药物曲安奈德、氢化可的松和吲哚美辛表明,正十六烷诱导的DNA合成和糖原代谢变化与cAMP浓度的初始下降有关。讨论了cAMP水平双相变化的意义,认为这可能是增生发展和维持的一种控制系统。