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地塞米松对大鼠和小鼠的抗过敏和抗炎作用的时间进程。

Time courses of the anti-anaphylactic and anti-inflammatory effects of dexamethasone in the rat and mouse.

作者信息

Church M K, Miller P

出版信息

Br J Pharmacol. 1978 Apr;62(4):481-6. doi: 10.1111/j.1476-5381.1978.tb07751.x.

Abstract

1 The time course of the activity of dexamethasone has been studied in a variety of anaphylactic and inflammatory reactions in the rat and the mouse. 2 The times of peak activity of dexamethasone, expressed as time between oral dosage and induction of response, and the approximate ED50 values (mg/kg) found were: anaphylactic bronchoconstriction in rats, 12-24 h, ED50 1.8; passive cutaneous anaphylaxis in rats, 6 h, ED50 0.04; cutaneous reactions to histamine in rats, 4 h, ED50 0.01; carrageenin-induced paw oedema in rats, 4 h, ED50 0.03; pinnal anaphylaxis in mice, 6 h, ED50 0.82; histamine-induced pinnal reactions in mice, 6 h, ED50 0.05. 3 In rats, the characteristics of the inhibitory effects of dexamethasone indicate a differential activity against anaphylactic and inflammatory reactions and between different types of inflammatory reactions. Possible reasons for these differences are discussed. 4 In mice there was little difference between the inhibition by dexamethasone of cutaneous allergic and histamine-induced reactions. 5 Pinnal anaphylaxis in mice was potentiated by dexamethasone given 1-2 h before challenge.

摘要
  1. 已在大鼠和小鼠的多种过敏反应和炎症反应中研究了地塞米松的活性时程。2. 地塞米松的活性峰值时间(以口服给药至反应诱导之间的时间表示)以及所发现的近似半数有效剂量(mg/kg)如下:大鼠过敏性支气管收缩,12 - 24小时,半数有效剂量1.8;大鼠被动皮肤过敏反应,6小时,半数有效剂量0.04;大鼠对组胺的皮肤反应,4小时,半数有效剂量0.01;角叉菜胶诱导的大鼠足肿胀,4小时,半数有效剂量0.03;小鼠耳廓过敏反应,6小时,半数有效剂量0.82;组胺诱导的小鼠耳廓反应,6小时,半数有效剂量0.05。3. 在大鼠中,地塞米松抑制作用的特征表明其对过敏反应和炎症反应以及不同类型炎症反应具有不同的活性。讨论了这些差异的可能原因。4. 在小鼠中,地塞米松对皮肤过敏反应和组胺诱导反应的抑制作用几乎没有差异。5. 在攻击前1 - 2小时给予地塞米松可增强小鼠的耳廓过敏反应。

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