Adams L W, Priestley G C
Department of Dermatology, Royal Infirmary, University of Edinburgh, Scotland, UK.
Arch Dermatol Res. 1988;280(2):114-8. doi: 10.1007/BF00417715.
A range of dermatologically useful drugs were added to human skin fibroblasts cultured in collagen lattices to assess possible effects on the rate of lattice contraction. Vitamin C, Vitamin E, phenytoin, sodium salicylate, D-penicillamine and dibutyryl c-AMP had no significant effect. Chlorhexidine acetate at 10 micrograms/ml arrested contraction after 24 h but this was related to its cytotoxicity. The antibiotics griseofulvin (2-16 micrograms/ml) and cycloheximide (5-30 micrograms/ml) caused dose-related inhibitions of contraction without affecting fibroblast viability. Four corticosteroids at 10 micrograms/ml inhibited contraction, clobetasol propionate having the greatest effect. On the other hand 4 retinoids at 10(-5) M enhanced contraction by up to 20%. As lattice contraction appears to model the contraction of skin wounds and there are broad parallels between the effects shown here of antiseptics, corticosteroids and the retinoids, and their reported influence on healing wounds, the lattice system may be a useful pharmacological screen for new compounds.
将一系列对皮肤科有用的药物添加到在胶原晶格中培养的人皮肤成纤维细胞中,以评估其对晶格收缩速率的可能影响。维生素C、维生素E、苯妥英、水杨酸钠、D-青霉胺和二丁酰环磷腺苷无显著影响。10微克/毫升的醋酸氯己定在24小时后可阻止收缩,但这与其细胞毒性有关。抗生素灰黄霉素(2 - 16微克/毫升)和环己酰亚胺(5 - 30微克/毫升)引起与剂量相关的收缩抑制,且不影响成纤维细胞活力。10微克/毫升的四种皮质类固醇抑制收缩,其中丙酸氯倍他索的作用最大。另一方面,10⁻⁵ M的四种维甲酸可使收缩增强高达20%。由于晶格收缩似乎模拟了皮肤伤口的收缩,并且此处显示的防腐剂、皮质类固醇和维甲酸的作用与它们对愈合伤口的报道影响之间存在广泛的相似性,因此晶格系统可能是一种用于新化合物的有用药理学筛选方法。