Gupta S K, Parker D, Turk J L
Int J Immunopharmacol. 1985;7(5):705-12. doi: 10.1016/0192-0561(85)90155-9.
Hydrocortisone acetate, injected subcutaneously in five doses in a depot producing vehicle, causes prolonged suppression of the ability of guinea pigs to produce a chronic inflammatory reaction in the peritoneal cavity and also of the tuberculin reaction. This suppression of the tuberculin reaction persists for at least 65 days after the last dose of hydrocortisone. Suppression of both peritoneal exudate and the tuberculin reaction was associated with a preferential depletion of macrophages at the reaction site. A similar regime had no effect on the ability of guinea pigs to manifest contact sensitivity reactions to 2,4-dinitrofluorobenzene although there was a similar drop in macrophages in the lesion. It appears that the effect of hydrocortisone on delayed hypersensitivity reactions is not directly related to the functional contribution of macrophages in the inflammatory reactions, and may be related to the site of the inflammatory reaction in the skin.
醋酸氢化可的松以五剂皮下注射于一种长效制剂载体中,可导致豚鼠产生腹腔慢性炎症反应的能力以及结核菌素反应受到长期抑制。在最后一剂氢化可的松注射后,这种对结核菌素反应的抑制至少持续65天。对腹腔渗出物和结核菌素反应的抑制均与反应部位巨噬细胞的优先耗竭有关。类似的给药方案对豚鼠表现出对2,4 -二硝基氟苯的接触敏感性反应的能力没有影响,尽管病变部位的巨噬细胞数量也有类似的减少。看来氢化可的松对迟发型超敏反应的作用并非直接与巨噬细胞在炎症反应中的功能贡献相关,可能与皮肤炎症反应的部位有关。