Saarni H, Jalkanen M, Hopsu-Havu V K
Br J Dermatol. 1980 Aug;103(2):167-73. doi: 10.1111/j.1365-2133.1980.tb06586.x.
The effect of five anti-inflammatory corticosteroids, i.e. hydrocortisone, hydrocortisone 17-butyrate, betamethasone 17-valerate, nicocortonide acetate and nicocortonide, on the synthesis of hyaluronic acid, sulphated glycosaminoglycans and collagen by cultured skin fibroblasts was studied. As inhibitors of all these parameters the steroids could be arranged in order hydrocortisone < hydrocortisone 17-butyrate < betamethasone 17-valerate, nicocortonide acetate and nicocortonide. The corticosteroid concentrations required for inhibition of hyaluronic acid were very low as compared to those required for inhibition of sulphated glycosaminoglycan and collagen synthesis.
研究了五种抗炎皮质类固醇,即氢化可的松、氢化可的松17 - 丁酸酯、倍他米松17 - 戊酸酯、醋酸尼考皮质酮和尼考皮质酮,对培养的皮肤成纤维细胞合成透明质酸、硫酸化糖胺聚糖和胶原蛋白的影响。作为所有这些参数的抑制剂,这些类固醇可以按以下顺序排列:氢化可的松<氢化可的松17 - 丁酸酯<倍他米松17 - 戊酸酯、醋酸尼考皮质酮和尼考皮质酮。与抑制硫酸化糖胺聚糖和胶原蛋白合成所需的浓度相比,抑制透明质酸所需的皮质类固醇浓度非常低。