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Cromoglycate and nedocromil enhanced the reactive oxygen species-dependent suppressions with but not without dexamethasone in ischaemic and histamine paw oedema of mice

机译:cromoglycate和nedocromil增强了地塞米松对小鼠局部缺血和组胺爪水肿的反应性氧依赖依赖性抑制作用

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摘要

Anti-inflammatory actions of two anti-allergic drugs, alone or with dexamethasone (Dex) were examined in two models, because inflammation is claimed to be important for allergic events, especially for asthma. Cromoglycate and nedocromil were tested in ischaemic- and histamineinduced paw oedema models of mice. These antiallergic drugs (1–100 mg/kg, i.p.) failed to suppress these oedemata, but enhanced the suppressions by a low dose of dexamethasone (0.1 mg/kg, s.c.) at 3–8 h after Dex injection. The mode of effects by anti-allergic drugs resembled that of a natural antioxidant (α-tocopherol, β-carotene etc.), and was different from that of an immunosuppressant like FK506. The enhancing potencies of the two anti-allergic drugs were similar at 6 h after Dex in both oedemata, and were diminished by superoxide dismutase (SOD) or catalase (i.p.). Cycloheximide completely abolished suppressions. Nedocromil, but not cromoglycate, inhibits inflammatory events. Therefore, there are common unknown actions by which the two anti-allergics enhance suppression by Dex. A possible mechanism of this action was supposed to enhance the superoxide and/or hydrogen peroxide-dependent glucocorticoid receptor (GR) signalling in the target cells.
机译:在两个模型中检查了两种抗过敏药单独或与地塞米松(Dex)的抗炎作用,因为据称炎症对于过敏事件(尤其是哮喘)很重要。在缺血和组胺引起的小鼠足水肿模型中测试了cromoglycate和nedocromil。这些抗过敏药(1–100 mg / kg,腹腔注射)未能抑制这些麻醉药,但在注射Dex后3–8小时使用低剂量地塞米松(0.1 mg / kg,皮下注射)增强了抑制作用。抗过敏药的作用方式类似于天然抗氧化剂(α-生育酚,β-胡萝卜素等),并且不同于免疫抑制剂(如FK506)。这两种抗过敏药的增强功效在两种食囊中的Dex后6 h相似,并且被超氧化物歧化酶(SOD)或过氧化氢酶(i.p.)减弱。环己酰亚胺完全取消了抑制作用。奈多克罗米可抑制炎症反应,但不会降低色甘酸。因此,存在两种抗过敏剂共同增强Dex抑制作用的常见未知作用。推测该作用的可能机制是增强靶细胞中超氧化物和/或过氧化氢依赖性糖皮质激素受体(GR)的信号传导。

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