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吸入肝素对特应性哮喘患者变应原诱导的早发和迟发哮喘反应的影响。

Effect of inhaled heparin on allergen-induced early and late asthmatic responses in patients with atopic asthma.

作者信息

Diamant Z, Timmers M C, van der Veen H, Page C P, van der Meer F J, Sterk P J

机构信息

Department of Pulmonology, University Hospital, Leiden, The Netherlands.

出版信息

Am J Respir Crit Care Med. 1996 Jun;153(6 Pt 1):1790-5. doi: 10.1164/ajrccm.153.6.8665036.

Abstract

Heparin possesses anti-inflammatory properties, which appeared to be dependent on the dose, timing, and the route of administration in animal studies. In asthma, a single dose of inhaled heparin only slightly reduced the early asthmatic response (EAR) but failed to protect against the late asthmatic response (LAR) to inhaled allergen. We studied the effect of multiple doses of inhaled heparin on the EAR and LAR to inhaled house-dust mite extract in eight stable asthmatics in a two-period, randomized, double-blind, crossover study. During both study periods, a standardized allergen challenge was performed and PC20 histamine was measured 24 h before and 24 h postallergen. Five doses of unfractionated heparin sodium (1,000 U/kg/dose) or placebo were inhaled 90 and 30 min preallergen, and 2, 4, and 6 h postallergen. Airway response was measured by FEV1, and the EAR (0-3 h) and LAR (3-10 h) were expressed as corresponding areas under the time-response curves (AUC). The acute effects of heparin and placebo on baseline FEV1 were not different (p > 0.07). Although not reaching significance, heparin attenuated the EAR by an average of 40% (mean AUC(0-3) +/- SEM: 29.5 +/- 6.0 [placebo] and 17.8 +/- 5.5% fall x h [heparin]; p = 0.08), while it significantly reduced the LAR by an average of 36% (AUC(3-10) +/- SEM: 169.3 +/- 20.0 [placebo] and 109.1 +/- 23.6% fall x h [heparin]; p = 0.005). We conclude that inhaled heparin reduces the LAR to allergen in asthmatic subjects, which may be due to its anti-inflammatory activity. Our finding suggests that heparin may have potential as anti-asthma therapy.

摘要

肝素具有抗炎特性,在动物研究中,其抗炎特性似乎取决于剂量、给药时间和给药途径。在哮喘方面,单剂量吸入肝素仅能轻微降低早期哮喘反应(EAR),但无法预防吸入变应原后的迟发性哮喘反应(LAR)。我们在一项为期两阶段的随机双盲交叉研究中,研究了多剂量吸入肝素对8名稳定期哮喘患者吸入屋尘螨提取物后的EAR和LAR的影响。在两个研究阶段,均进行了标准化变应原激发试验,并在变应原激发前24小时和激发后24小时测量PC20组胺。在变应原激发前90分钟和30分钟以及激发后2、4和6小时吸入五剂未分级肝素钠(1000 U/kg/剂)或安慰剂。通过第一秒用力呼气量(FEV1)测量气道反应,EAR(0 - 3小时)和LAR(3 - 10小时)表示为时间-反应曲线下的相应面积(AUC)。肝素和安慰剂对基线FEV1的急性影响无差异(p > 0.07)。虽然未达到显著水平,但肝素使EAR平均降低了40%(平均AUC(0 - 3) +/- 标准误:29.5 +/- 6.0 [安慰剂] 和17.8 +/- 5.5%下降×小时 [肝素];p = 0.08),而它使LAR平均显著降低了36%(AUC(3 - 10) +/- 标准误:169.3 +/- 20.0 [安慰剂] 和109.1 +/- 23.6%下降×小时 [肝素];p = 0.005)。我们得出结论,吸入肝素可降低哮喘患者对变应原的LAR,这可能归因于其抗炎活性。我们的研究结果表明,肝素可能具有作为抗哮喘治疗药物的潜力。

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