Holgate S T
Eur J Respir Dis Suppl. 1986;147:149-59.
The recognition that inflammatory events in the airways play a key role in the pathogenesis of asthma has led to a relentless search for pharmacological agents which modify these processes. Nedocromil sodium (Tilade) represents one such agent. Nedocromil sodium, when inhaled by patients with asthma (0.05-0.50% nebulized, 0.5-4.0 mg m.d.i.), has been shown to inhibit immediate bronchoconstriction provoked by challenges with allergen (10 studies), exercise (five studies), isocapnic hyperventilation, fog and sulphur dioxide (one study each) and adenosine (two studies). With these challenges, inhibition of bronchoconstriction exhibited dose-dependency up to 4 mg, with nedocromil sodium being up to four times more potent than sodium cromoglycate. When inhaled prior to allergen provocation, nedocromil sodium inhibited the late asthmatic reaction; when taken regularly during the pollen season, it attenuated the allergen-induced increase in non-specific bronchial responsiveness. The efficacy of nedocromil sodium (4 mg q.i.d.) in the treatment of clinical asthma was initially shown in four open studies and subsequently confirmed in nine double-blind, placebo-controlled 4-12 week studies on patients with seasonal and perennial asthma. Further clinical trials (eight studies) identified some difficulty in replacing inhaled corticosteroids with nedocromil sodium, especially if the corticosteroids were reduced rapidly (four studies). However, two studies have shown that nedocromil sodium produced further improvement in asthma symptoms when used in addition to bronchodilators and inhaled corticosteroids. Treatment with nedocromil sodium (4 mg q.i.d.) for up to 52 weeks demonstrated a progressive reduction in bronchodilator usage throughout the whole treatment period. During clinical assessment, nedocromil sodium was well tolerated, side-effects being unpleasant taste, nausea and headache. In most cases the adverse reactions were mild and transient, although in approximately 3% of patients they resulted in withdrawal from clinical trials. Thus, nedocromil sodium is a novel drug of proven efficacy in the treatment of asthma. Its position in the therapeutic armamentarium is likely to be as an adjunct to bronchodilators and inhaled steroids, to produce improvement in symptoms beyond that achieved with the already established drugs.
气道炎症事件在哮喘发病机制中起关键作用这一认识,促使人们不断寻找能够改变这些过程的药物。奈多罗米钠(替乐迪)就是这样一种药物。哮喘患者吸入奈多罗米钠(雾化吸入0.05 - 0.50%,定量吸入器吸入0.5 - 4.0毫克)后,已证实其能抑制由过敏原激发(10项研究)、运动激发(5项研究)、等碳酸过度通气激发、雾和二氧化硫激发(各1项研究)以及腺苷激发(2项研究)所引发的即刻支气管收缩。对于这些激发试验,在剂量高达4毫克时,支气管收缩的抑制呈现剂量依赖性,奈多罗米钠的效力比色甘酸钠高4倍。在过敏原激发前吸入奈多罗米钠,可抑制迟发性哮喘反应;在花粉季节定期服用时,可减轻过敏原诱导的非特异性支气管反应性增加。奈多罗米钠(4毫克,每日4次)治疗临床哮喘的疗效最初在4项开放性研究中得到证实,随后在9项针对季节性和常年性哮喘患者的双盲、安慰剂对照的4 - 12周研究中得到确认。进一步的临床试验(8项研究)发现,用奈多罗米钠替代吸入性糖皮质激素存在一些困难,尤其是在快速减少糖皮质激素用量时(4项研究)。然而,两项研究表明,奈多罗米钠与支气管扩张剂和吸入性糖皮质激素联合使用时,能进一步改善哮喘症状。用奈多罗米钠(4毫克,每日4次)治疗长达52周,结果显示在整个治疗期间支气管扩张剂的使用量逐渐减少。在临床评估中,奈多罗米钠耐受性良好,副作用包括味觉不适、恶心和头痛。在大多数情况下,不良反应轻微且短暂,尽管约3%的患者因不良反应退出临床试验。因此,奈多罗米钠是一种已证实对哮喘治疗有效的新型药物。其在治疗药物中的地位可能是作为支气管扩张剂和吸入性类固醇的辅助药物,以产生比现有药物更大的症状改善效果。