Dal Negro Roberto W
Lung Department, Orlandi General Hospital, Verona, Italy.
Lung. 2008;186 Suppl 1:S70-3. doi: 10.1007/s00408-007-9065-3. Epub 2008 Jan 10.
Erdosteine is a multifactorial drug currently used in COPD for its rheologic activity on bronchial secretions and its positive effects on bacterial adhesiveness. Erdosteine produces an active metabolite (Met 1) which was shown to produce antioxidant effects during the respiratory burst of human PMNs, due to the presence of an SH group. The substantial antitussive effects of erdosteine were first documented in clinical trials even though mucolytic agents are regarded as not consistently effective in ameliorating cough in patients with bronchitis, although they may be of benefit to this population in other ways. Actually, a mucolytic drug could exert antitussive effects if it also affects mucus consistency and enhances ciliary function. In the last decade, data from several studies on animal models pointed to the possible antitussive and anti-inflammatory properties of erdosteine and an indirect anti-inflammatory mechanism of action was suggested. Recently, data from some controlled versus placebo studies documented the antioxidant properties of erdosteine in humans and in current smokers with COPD. The mechanism of action was described as related to erdosteine's ability to inhibit some inflammatory mediators and some pro-inflammatory cytokines that are specifically involved in oxidative stress. As oxidative stress is also presumed to impair beta-adrenoceptor function and contribute to airway obstruction, specific controlled studies recently investigated the effect of antioxidant intervention on short-term airway response to salbutamol in nonreversible COPD, according to a double-blind design versus placebo and NAC. Only erdosteine consistently restored a significant short-term reversibility in COPD subjects, previously unresponsive to beta(2) adrenergics. This peculiar activity of erdosteine (to our knowledge never previously assessed) proved related to the ROS scavenging activity (which actually proved equal to that of N), and its significant inhibiting effect on lipoperoxidation (8-isoprostane) proved discriminant between treatments, with antioxidant and anti-inflammatory effects the main determinants of the erdosteine multifactorial properties. In addition, antitussive effects may be regarded as related to its anti-inflammatory properties via the improvement of mucociliary clearance and the reduction of chemokines from epithelial cells. Finally, a sort of "sensitization" of 2-adrenoceptors can also be speculated due to the same mechanisms of action; if confirmed by further controlled studies, this particular property would suggest a novel therapeutic role of erdosteine in COPD.
厄多司坦是一种多效药物,目前用于慢性阻塞性肺疾病(COPD),因其对支气管分泌物具有流变学活性以及对细菌黏附性有积极作用。厄多司坦产生一种活性代谢物(Met 1),由于含有巯基,该代谢物在人中性粒细胞呼吸爆发期间表现出抗氧化作用。尽管黏液溶解剂在改善支气管炎患者咳嗽方面被认为效果不一,但厄多司坦显著的镇咳作用最早在临床试验中得到证实,不过它们可能在其他方面对该人群有益。实际上,如果一种黏液溶解药物还能影响黏液黏稠度并增强纤毛功能,那么它可能发挥镇咳作用。在过去十年中,多项动物模型研究的数据表明厄多司坦可能具有镇咳和抗炎特性,并提出了一种间接的抗炎作用机制。最近,一些对照与安慰剂研究的数据证明了厄多司坦在人类以及COPD现吸烟者中的抗氧化特性。其作用机制被描述为与厄多司坦抑制某些炎症介质和一些特别参与氧化应激的促炎细胞因子的能力有关。由于氧化应激也被认为会损害β - 肾上腺素能受体功能并导致气道阻塞,最近的特定对照研究根据双盲设计,对比安慰剂和N - 乙酰半胱氨酸(NAC),调查了抗氧化干预对不可逆COPD患者短期气道对沙丁胺醇反应的影响。只有厄多司坦能持续恢复COPD受试者先前对β₂肾上腺素能药物无反应的显著短期可逆性。厄多司坦的这种特殊活性(据我们所知以前从未评估过)被证明与活性氧清除活性有关(实际上证明与NAC的活性氧清除活性相当),并且其对脂质过氧化(8 - 异前列腺素)的显著抑制作用在各治疗组之间具有判别性,抗氧化和抗炎作用是厄多司坦多效特性的主要决定因素。此外,镇咳作用可能通过改善黏液纤毛清除和减少上皮细胞趋化因子而被认为与其抗炎特性有关。最后,由于相同的作用机制,还可以推测存在一种对β - 肾上腺素能受体的“致敏”作用;如果进一步的对照研究证实这一特性,那么厄多司坦在COPD中可能具有新的治疗作用。