Schoepe Stefanie, Schäcke Heike, Asadullah Khusru
Target Discovery; Global Drug Discovery; Bayer Schering Pharma AG; Berlin, Germany.
Dermatoendocrinol. 2011 Jul;3(3):175-9. doi: 10.4161/derm.3.3.15065. Epub 2011 Jul 1.
Topical glucocorticoids are highly anti-inflammatory effective but limited by their side effect potential, with skin atrophy being the most prominent one. Thus, determining the atrophogenic potential of novel compounds targeting the glucocorticoid receptor is important. Significant progress in the understanding of glucocorticoid receptor mediated molecular action has been made providing the basis for novel glucocorticoid receptor ligands with a potentially superior effect/side effect profile. Such compounds, however, need to be tested. The present gold standard for the reliable prediction of glucocorticoid induced skin atrophy are still in vivo models, however, in vitro models may replace them to some extent in the future. Indeed, advances in technologies to determine the atrophogenic potential of compounds in vitro has been made recently and promising novel test models like the human full thickness skin models are emerging. Their full predictive value, however, needs to be further evaluated. Currently, a screening approach starting with a combination of several in vitro test systems followed by subsequent testing of the most promising compounds in rodent models is recommended prior entering clinical studies with selected development compounds.
局部用糖皮质激素具有高度抗炎作用,但受其潜在副作用限制,其中皮肤萎缩最为突出。因此,确定靶向糖皮质激素受体的新型化合物的致萎缩潜力很重要。在理解糖皮质激素受体介导的分子作用方面已取得重大进展,为具有潜在更优疗效/副作用特征的新型糖皮质激素受体配体奠定了基础。然而,此类化合物仍需进行测试。目前可靠预测糖皮质激素诱导皮肤萎缩的金标准仍是体内模型,不过体外模型未来可能在一定程度上取代它们。事实上,最近在体外确定化合物致萎缩潜力的技术方面取得了进展,诸如人全层皮肤模型等有前景的新型测试模型正在出现。然而,它们的全部预测价值仍需进一步评估。目前,建议在选用研发化合物进入临床研究之前,先采用多种体外测试系统相结合的筛选方法,随后在啮齿动物模型中对最有前景的化合物进行测试。