Kidney J C, Fuller R W, Worsdell Y M, Lavender E A, Chung K F, Barnes P J
Department of Thoracic Medicine, National Heart and Lung Institute, London.
Thorax. 1993 Feb;48(2):130-3. doi: 10.1136/thx.48.2.130.
Potassium (K+) channel activators, such as cromakalim, open ATP sensitive K+ channels and relax airway smooth muscle in vitro and inhibit induced bronchoconstriction in vivo in animals. The prolonged half life of cromakalim gives it potential as an oral bronchodilator. The effect of orally administered BRL 38227 (the active enantiomer of cromakalim), at doses of 0.125, 0.25, and 0.5 mg, on airway function and airway responsiveness to histamine and methacholine has been investigated in asthmatic patients.
Seventeen patients with asthma were studied in three separate randomised double blind, placebo controlled studies. In the first study eight patients with moderately severe asthma were given 0.125, 0.25, and 0.5 mg of BRL 38227 or placebo, and responses to histamine were assessed before and five hours after treatment. In the second study responses to methacholine were measured before and five hours after 0.125 and 0.5 mg of BRL 38227 or placebo were given to nine patients with mild asthma. In the third study the effect of 0.5 mg of BRL 38227 or placebo was assessed in eight patients with mild asthma. Responses to histamine were measured before treatment and two and five hours after treatment. To provide a positive control study eight subjects who had taken part in studies 1 and 3 were also given oral salbutamol (8 mg) in a placebo controlled, double blind study. Responses to histamine were assessed before and two hours after treatment.
BRL 38227 did not cause significant bronchodilatation or changes in airway responsiveness in any of the studies. Headache was reported in 19 of 25 of patients receiving (in some cases twice) 0.5 mg of BRL 38227. By contrast, oral salbutamol gave significant protection against histamine challenge (geometric mean 2.23 doubling dilutions).
After a single oral dose of BRL 38227 no beneficial effect on airway function was detected, despite a high incidence of side effects, which indicates that the orally administered K+ channel activator BRL 38227 may not be useful in the management of asthma.
钾(K+)通道激活剂,如克罗卡林,可打开ATP敏感性钾通道,在体外使气道平滑肌松弛,并在动物体内抑制诱发的支气管收缩。克罗卡林较长的半衰期使其具有作为口服支气管扩张剂的潜力。已在哮喘患者中研究了口服剂量为0.125、0.25和0.5毫克的BRL 38227(克罗卡林的活性对映体)对气道功能以及气道对组胺和乙酰甲胆碱反应性的影响。
在三项单独的随机双盲、安慰剂对照研究中对17例哮喘患者进行了研究。在第一项研究中,8例中度重度哮喘患者分别给予0.125、0.25和0.5毫克的BRL 38227或安慰剂,并在治疗前和治疗后5小时评估对组胺的反应。在第二项研究中,9例轻度哮喘患者在给予0.125和0.5毫克的BRL 38227或安慰剂前和后5小时测量对乙酰甲胆碱的反应。在第三项研究中,对8例轻度哮喘患者评估了0.5毫克的BRL 38227或安慰剂的效果。在治疗前以及治疗后2小时和5小时测量对组胺的反应。为了进行阳性对照研究,在一项安慰剂对照的双盲研究中,还对参与研究1和3的8名受试者给予了口服沙丁胺醇(8毫克)。在治疗前和治疗后2小时评估对组胺的反应。
在任何一项研究中,BRL 38227均未引起明显的支气管扩张或气道反应性变化。在接受(某些情况下为两次)0.5毫克BRL 38227的25例患者中有19例报告了头痛。相比之下,口服沙丁胺醇对组胺激发有显著的保护作用(几何平均倍增稀释度为2.23)。
单次口服BRL 38227后,未检测到对气道功能有有益作用,尽管副作用发生率较高,这表明口服钾通道激活剂BRL 38227可能对哮喘治疗无效。