Uphill P F, Poole A
Arzneimittelforschung. 1981;31(3):462-6.
A comparison was made of the ability of guinea pig alveolar macrophages, which had been pretreated with hydrocortisone acetate, beclomethasone dipropionate or a corticosteroid substitute pregn-4-ene-3,20-dione-21-thiol-11 beta,17 alpha-dihydroxy-21-pivalate (tixocortol pivalate, JO 1016, Pivalone), to phagocytose and lyse Staphylococcus aureus or Candida albicans. The three drugs had different patterns of effect on phagocytosis and lysis. Hydrocortisone acetate had little effect on the phagocytosis of Staph. aureus at any dose level tested, but the two higher concentrations slightly inhibited intracellular lysis; phagocytosis of C. albicans was inhibited initially but increased at 5 h. Both beclomethasone dipropionate and tixocortol pivalate caused an initial stimulation of phagocytosis and lysis of Staph. aureus. Ingestion of C. albicans was increased in macrophages pretreated with beclomethasone dipropionate, but their fungicidal activity was unchanged. Pretreatment with tixocortol pivalate stimulated the initial phagocytosis of C. albicans but continued uptake on prolonged incubation was inhibited. Lysis of the ingested organisms was not markedly affected. Since the production of any effect on the phagocytic and lytic activity of alveolar macrophages required much higher levels of tixocortol pivalate than of either of the other two drugs, it is suggested that in clinical use correspondingly higher doses of tixocortol pivalate could be given without danger of affecting either phagocytic activity or the immune response.
对经醋酸氢化可的松、二丙酸倍氯米松或皮质类固醇替代物孕-4-烯-3,20-二酮-21-硫醇-11β,17α-二羟基-21-新戊酸酯(替可的松新戊酸酯,JO 1016,Pivalone)预处理的豚鼠肺泡巨噬细胞吞噬和裂解金黄色葡萄球菌或白色念珠菌的能力进行了比较。这三种药物对吞噬作用和裂解作用有不同的影响模式。在任何测试剂量水平下,醋酸氢化可的松对金黄色葡萄球菌的吞噬作用影响很小,但两个较高浓度略微抑制细胞内裂解;白色念珠菌的吞噬作用最初受到抑制,但在5小时时增加。二丙酸倍氯米松和替可的松新戊酸酯均引起金黄色葡萄球菌吞噬作用和裂解的初始刺激。用二丙酸倍氯米松预处理的巨噬细胞中白色念珠菌的摄取增加,但其杀真菌活性未改变。用替可的松新戊酸酯预处理刺激了白色念珠菌的初始吞噬作用,但长时间孵育后的持续摄取受到抑制。摄入生物体的裂解没有受到明显影响。由于对肺泡巨噬细胞吞噬和裂解活性产生任何影响所需的替可的松新戊酸酯水平远高于其他两种药物中的任何一种,因此建议在临床使用中可以给予相应更高剂量的替可的松新戊酸酯而不会有影响吞噬活性或免疫反应的风险。