Polosa R, Rajakulasingam K, Prosperini G, Magrì S, Mastruzzo C, Holgate S T
Istituto Malattie Apparato Respiratorio, Università di Catania, Italy.
Eur Respir J. 1995 Apr;8(4):593-9.
Inhaled frusemide protects asthmatic airways against a wide variety of bronchoconstrictor stimuli by unknown mechanisms. To investigate whether inhaled loop diuretics modulate baseline bronchial responsiveness, a randomized, double-blind, placebo-controlled study was conducted to test the ability of frusemide (40 mg) and bumetanide (2 mg) to displace concentration-response curves with methacholine in 14 healthy volunteers. In addition, separate randomized, double-blind studies were carried out to evaluate the effects of oral flurbiprofen, a potent cyclo-oxygenase inhibitor, on the protective action of frusemide against methacholine-induced bronchoconstriction. Inhaled loop diuretics significantly increased the provocative concentration of methacholine causing a 15% decrease in forced expiratory volume in one second (PC15FEV1) from the geometric mean (range) value of 58.6 (9.2-233) mg.ml-1 after placebo administration, to 129 (13.8-505) and to 106 (6.6-510) mg.ml-1 after administration of frusemide and bumetanide, respectively. Similar results were obtained when data from partial flow-volume curves were used for analysis. In the eight subjects studied, pretreatment with oral placebo and inhaled frusemide reduced airway responsiveness to methacholine, with a geometric mean (range) PC15FEV1 value of 116 (25.4-405) mg.ml-1, and premedication with oral flurbiprofen abolished this protective effect, the geometric mean (range) PC15FEV1 methacholine being reduced to a value of 50.3 (16.6-189) mg.ml-1. In addition, oral flurbiprofen alone failed to alter airway responsiveness to methacholine. In view of these findings, it is suggested that bronchoprotective prostaglandins may mediate the effects of loop diuretics against methacholine-induced bronchoconstriction in man.
吸入用速尿可通过未知机制保护哮喘气道免受多种支气管收缩刺激。为研究吸入性袢利尿剂是否调节基线支气管反应性,进行了一项随机、双盲、安慰剂对照研究,以测试速尿(40毫克)和布美他尼(2毫克)在14名健康志愿者中用乙酰甲胆碱置换浓度-反应曲线的能力。此外,还进行了单独的随机、双盲研究,以评估强效环氧化酶抑制剂口服氟比洛芬对速尿抗乙酰甲胆碱诱导的支气管收缩保护作用的影响。吸入性袢利尿剂显著增加了引起一秒用力呼气量降低15%(PC15FEV1)的乙酰甲胆碱激发浓度,从安慰剂给药后几何平均值(范围)58.6(9.2 - 233)毫克·毫升-1,分别增至速尿给药后的129(13.8 - 505)毫克·毫升-1和布美他尼给药后的106(6.6 - 510)毫克·毫升-1。当使用部分流量-容积曲线数据进行分析时,得到了类似结果。在研究的8名受试者中,口服安慰剂和吸入速尿预处理降低了气道对乙酰甲胆碱的反应性,PC15FEV1几何平均值(范围)为116(25.4 - 405)毫克·毫升-1,口服氟比洛芬预处理消除了这种保护作用,乙酰甲胆碱的PC15FEV1几何平均值(范围)降至50.3(16.6 - 189)毫克·毫升-1。此外,单独口服氟比洛芬未能改变气道对乙酰甲胆碱的反应性。鉴于这些发现,提示支气管保护性前列腺素可能介导袢利尿剂对人乙酰甲胆碱诱导的支气管收缩的作用。