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吸入低分子量肝素预防运动诱发性支气管收缩

Prevention of exercise-induced bronchoconstriction by inhaled low-molecular-weight heparin.

作者信息

Ahmed T, Gonzalez B J, Danta I

机构信息

Division of Pulmonary Disease, University of Miami School of Medicine, Mount Sinai Medical Center, Miami Beach, Florida, USA.

出版信息

Am J Respir Crit Care Med. 1999 Aug;160(2):576-81. doi: 10.1164/ajrccm.160.2.9812076.

Abstract

Because many biological actions of heparin including the antiallergic activity are molecular weight dependent, we hypothesized that low-molecular-weight heparin (LMWH) may have greater potency in attenuating exercise-induced bronchoconstriction (EIB). Therefore, in the present investigation we studied the effects of inhaled LMWH, enoxaparin, and unfractionated heparin on EIB in subjects with asthma. Thirteen asthmatic subjects performed a standardized exercise challenge on a treadmill to document the presence of EIB. The workload was increased until 85% of predicted maximal heart rate was achieved, and the exercise was sustained at that workload for 10 min. EIB was assessed by measuring FEV(1) before and immediately after the exercise. On five different experiment days the subjects were pretreated with 4 ml of aerosolized heparin (80,000 units = 7.5 mg/kg), placebo, or 3 different doses of enoxaparin (0.5 mg/kg, 1 mg/kg, 2 mg/kg) in a double-blind, randomized, crossover design, and exercise challenge was performed 45 min later. Bronchial provocation with methacholine was also performed in five subjects on two additional days after pretreatment with either placebo or inhaled enoxaparin (2 mg/kg), and venous blood was obtained for analysis of plasma antifactor Xa. Postexercise, the maximal decreases in FEV(1) (mean +/- SE) were 30 +/- 4% and 29 +/- 5% on control and placebo days. The exercise-induced decreases in FEV(1) were inhibited by 31% with heparin (DeltaFEV(1) = 20 +/- 4%); and by 28%, 38%, and 48% by enoxaparin at doses of 0.5 mg/kg (DeltaFEV(1) = 21 +/- 5%), 1 mg/kg (DeltaFEV(1) = 18 +/- 5%), and 2 mg/kg (DeltaFEV(1) = 15 +/- 3%), respectively (p < 0.05). The inhibitory effect of 0.5 mg/kg dose of enoxaparin was comparable to heparin (7.5 mg/kg), whereas 2 mg/ kg dose of enoxaparin was the most potent. Inhaled enoxaparin failed to modify the bronchoconstrictor response to methacholine, and did not change the plasma antifactor Xa activity. These data demonstrate that inhaled enoxaparin prevents EIB in a dose-dependent manner; and its antiasthmatic activity is independent of its effect on plasma antifactor Xa activity.

摘要

由于肝素的许多生物学作用(包括抗过敏活性)都依赖于分子量,我们推测低分子量肝素(LMWH)在减轻运动诱发性支气管收缩(EIB)方面可能具有更强的效力。因此,在本研究中,我们研究了吸入性LMWH依诺肝素和普通肝素对哮喘患者EIB的影响。13名哮喘患者在跑步机上进行标准化运动激发试验以证实EIB的存在。工作量逐渐增加,直至达到预测最大心率的85%,并在该工作量下持续运动10分钟。通过在运动前和运动后立即测量第一秒用力呼气量(FEV₁)来评估EIB。在五个不同的实验日,受试者采用双盲、随机、交叉设计,预先接受4毫升雾化肝素(80,000单位 = 7.5毫克/千克)、安慰剂或3种不同剂量的依诺肝素(0.5毫克/千克、1毫克/千克、2毫克/千克)治疗,45分钟后进行运动激发试验。在另外两天,对5名受试者在预先接受安慰剂或吸入性依诺肝素(2毫克/千克)治疗后进行乙酰甲胆碱支气管激发试验,并采集静脉血分析血浆抗Xa因子。运动后,在对照日和安慰剂日,FEV₁的最大降幅(均值±标准误)分别为30±4%和29±5%。肝素(ΔFEV₁ = 20±4%)可使运动诱导的FEV₁下降受到31%的抑制;依诺肝素0.5毫克/千克(ΔFEV₁ = 21±5%)、1毫克/千克(ΔFEV₁ = 18±5%)和2毫克/千克(ΔFEV₁ = 15±3%)剂量分别可使下降受到28%、38%和48%的抑制(p < 0.05)。依诺肝素0.5毫克/千克剂量的抑制作用与肝素(7.5毫克/千克)相当,而2毫克/千克剂量的依诺肝素效力最强。吸入性依诺肝素未能改变对乙酰甲胆碱的支气管收缩反应,也未改变血浆抗Xa因子活性。这些数据表明,吸入性依诺肝素以剂量依赖的方式预防EIB;其抗哮喘活性与其对血浆抗Xa因子活性的影响无关。

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