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致敏后3周和8周豚鼠中类花生酸在偏苯三酸酐结合物诱导的气流阻塞和气道血浆渗出中的作用

Role of eicosanoids in airflow obstruction and airway plasma exudation induced by trimellitic anhydride-conjugate in guinea-pigs 3 and 8 weeks after sensitization.

作者信息

Arakawa H, Lötvall J, Lindén A, Kawikova I, Löfdahl C G, Skoogh B E

机构信息

Lung Pharmacology Group, University of Göteborg, Gothenburg, Sweden.

出版信息

Clin Exp Allergy. 1994 Jun;24(6):582-9. doi: 10.1111/j.1365-2222.1994.tb00956.x.

Abstract

Trimellitic anhydride (TMA) is a low molecular weight chemical which can cause occupational asthma. We studied the role of eicosanoids in airway responses to TMA at different times after sensitization in actively sensitized guinea-pigs. Sensitization was performed by two intradermal injections of free TMA (0.1 ml of 0.3% TMA in corn oil). At 3 and 8 weeks after sensitization, the guinea-pigs were anaesthetized and challenged with intratracheal instillation of 0.5% TMA conjugated to guinea-pig serum albumin (TMA-GPSA; 50 microliters). Lung resistance (RL) was measured to assess airflow obstruction, and the tissue content of Evans Blue dye was measured to assess airway plasma exudation. Intratracheal instillation of TMA-GPSA induced a slowly progressing increase in RL, reaching a peak at approximately 3.5 min after the challenge (6.0 +/- 2.0 cm H2O/ml/s in the 3-week group and 3.8 +/- 0.6 in the 8-week group). Pretreatment before challenge with pyrilamine (anti-histamine: 2 mg/kg, intravenously) slowed the onset of the increase in RL following challenge with TMA-GPSA, and significantly attenuated the peak response. A combination of pyrilamine and ICI-192,605 (thromboxane receptor antagonist; 0.5 mg/kg, intravenously) completely abolished the increase in RL in both week groups. A combination of pyrilamine and ICI-198,615 (leukotriene C4/D4/E4 receptor antagonist: 0.5 mg/kg, intravenously) did not further attenuate the increase in RL compared with pretreatment with pyrilamine alone, but the induced Evans Blue dye extravasation was completely inhibited in the 3-week group, whereas a remaining extravasation was observed in the 8-week group.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

偏苯三酸酐(TMA)是一种可引发职业性哮喘的低分子量化学物质。我们研究了在主动致敏的豚鼠中,致敏后不同时间点类花生酸在气道对TMA反应中的作用。通过两次皮内注射游离TMA(0.1 ml含0.3% TMA的玉米油溶液)进行致敏。在致敏后3周和8周,将豚鼠麻醉,经气管内滴注与豚鼠血清白蛋白结合的0.5% TMA(TMA-GPSA;50微升)进行激发。测量肺阻力(RL)以评估气流阻塞情况,并测量伊文思蓝染料的组织含量以评估气道血浆渗出。经气管内滴注TMA-GPSA可使RL缓慢上升,激发后约3.5分钟达到峰值(3周组为6.0±2.0 cm H2O/ml/s,8周组为3.8±0.6)。在激发前用吡苄明(抗组胺药:2 mg/kg,静脉注射)预处理可减缓TMA-GPSA激发后RL上升的起始速度,并显著减弱峰值反应。吡苄明与ICI-192,605(血栓素受体拮抗剂;0.5 mg/kg,静脉注射)联合使用可完全消除两个周组中RL的增加。吡苄明与ICI-198,615(白三烯C4/D4/E4受体拮抗剂:0.5 mg/kg,静脉注射)联合使用,与单独用吡苄明预处理相比,并未进一步减弱RL的增加,但在3周组中可完全抑制伊文思蓝染料的渗出,而在8周组中仍观察到有残留渗出。(摘要截选至250字)

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