Langhoff E, Ladefoged J
Eur J Clin Pharmacol. 1983;25(4):459-62. doi: 10.1007/BF00542111.
Natural and synthetic steroids and mineralocorticoids were tested for their in vitro suppressive activity on phytohemagglutinin (PHA) stimulated lymphocytes. Three different (p less than 0.05) groups were identified. Methylprednisolone and betamethasone were very potent, dexamethasone, hydrocortisone and prednisolone were of intermediate potency, and aldosterone, prednisone and the metabolites of hydrocortisone were of low potency. In general, synthetic steroids were considerably more potent than naturally occurring compounds, but the relatively low potency of dexamethasone was unexpected. These in vitro findings rank glucocorticoid potency differently from the relative anti-inflammatory activities reported in the literature.
对天然和合成类固醇以及盐皮质激素进行了测试,以考察它们对植物血凝素(PHA)刺激的淋巴细胞的体外抑制活性。确定了三个不同的(p<0.05)组。甲泼尼龙和倍他米松活性很强,地塞米松、氢化可的松和泼尼松龙活性中等,而醛固酮、泼尼松和氢化可的松的代谢产物活性较弱。一般来说,合成类固醇的活性比天然化合物强得多,但地塞米松相对较低的活性出乎意料。这些体外研究结果对糖皮质激素活性的排序与文献报道的相对抗炎活性不同。