Tanabe J, Watanabe M, Mue S, Ohuchi K
Department of Pathophysiological Biochemistry, Faculty of Pharmaceutical Sciences, Tohoku University, Miyagi, Japan.
Eur J Pharmacol. 1995 Sep 25;284(3):257-63. doi: 10.1016/0014-2999(95)00336-j.
In the air pouch-type allergic inflammation model in rats, when the infiltrated leukocytes in the pouch fluid collected 4 h after antigen challenge were incubated, neutrophil chemotactic activity in the conditioned medium increased time-dependently. They produced neutrophil chemotactic factors, viz. leukocyte-derived neutrophil chemotactic factor (LDNCF)-2, a major component, and LDNCF-1, a minor component. When the infiltrated leukocytes were incubated in the presence of dexamethasone, neutrophil chemotactic activity in the conditioned medium decreased in a concentration-dependent manner, and production of LDNCF-2 and LDNCF-1 was inhibited. Because purified LDNCF-2 had been found to be identical with rat macrophage inflammatory protein 2 (MIP-2), effects of dexamethasone on the level of MIP-2 mRNA in the leukocytes were investigated. Using the reverse transcription-polymerase chain reaction technique, it was demonstrated that dexamethasone suppressed the level of MIP-2 mRNA in the leukocytes. These results indicate that dexamethasone inhibits MIP-2 production at the transcription level.
在大鼠气袋型变应性炎症模型中,抗原激发4小时后收集气袋液中的浸润白细胞进行孵育,条件培养基中的中性粒细胞趋化活性呈时间依赖性增加。它们产生中性粒细胞趋化因子,即主要成分白细胞源性中性粒细胞趋化因子(LDNCF)-2和次要成分LDNCF-1。当浸润白细胞在地塞米松存在下孵育时,条件培养基中的中性粒细胞趋化活性呈浓度依赖性降低,且LDNCF-2和LDNCF-1的产生受到抑制。由于已发现纯化的LDNCF-2与大鼠巨噬细胞炎性蛋白2(MIP-2)相同,因此研究了地塞米松对白细胞中MIP-2 mRNA水平的影响。使用逆转录-聚合酶链反应技术证明,地塞米松可抑制白细胞中MIP-2 mRNA的水平。这些结果表明,地塞米松在转录水平抑制MIP-2的产生。