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囊性纤维化患者气道分泌物的物理和功能特性——治疗方法

Physical and functional properties of airway secretions in cystic fibrosis--therapeutic approaches.

作者信息

Puchelle E, de Bentzmann S, Zahm J M

机构信息

INSERM U 314, CHR Maison-Blanche, Reims, France.

出版信息

Respiration. 1995;62 Suppl 1:2-12. doi: 10.1159/000196486.

Abstract

The airway secretions which line the respiratory tract form a biphasic layer composed of an aqueous 'sol' layer and a more superficial 'gel' layer. In the sol layer, also described as the 'periciliary' layer or 'airway surface fluid', the cilia beat and relax. The lubricant sol layer enables the gel mucus present at the tips of the cilia to be transported by the ciliary beating of the ciliated cells. Due to difficulties with sampling, little is known about the physical and biochemical properties of the sol layer. The gel layer is composed of high molecular weight glycoproteins (mucins) linked with proteins and lipids. They form a gel network with a high water content (95%) and rheologic and physical properties (viscoelasticity, adhesivity) adapted in normal conditions to protect the airway mucosa, particularly through mucociliary transport. The adhesive properties of mucus, which are influenced by its lipid composition and degree of hydration, are very important in controlling the efficacy of mucus transport through ciliary activity and coughing. An intermediate viscosity and elasticity is required for optimal mucociliary transport. In obstructive airway diseases, either of genetic origin, such as cystic fibrosis (CF), or acquired (acute or chronic bronchitis), and particularly during inflammatory and infectious episodes, mucus dehydration is associated with an increase in secreted or transudated molecules and with marked augmentation of DNA content. These abnormalities contribute to the increased viscosity and adhesivity of the airway secretions and are responsible for their abnormally low transport rate by ciliary activity and for inefficient cough clearance. In view of these alterations in the physical and functional properties of CF airway secretions, pharmacologic approaches should aim to rehydrate the mucus and to restore normal mucociliary or cough transport by stimulating chloride ion secretion (i.e. using UTP or ATP associated with amiloride in order to block sodium ion and water reabsorption). During acute episodes of infection, recombinant human DNase (rhDNase) may rapidly prevent mucus stasis by improving its rheologic properties. Lubrication of the mucus at the sol phase interface by 'surfactant' therapy may also represent a very promising therapeutic perspective to reduce the hyperviscosity and hyperadhesivity of airway secretions.

摘要

呼吸道内的气道分泌物形成了一个双相层,由水性的“溶胶”层和较浅的“凝胶”层组成。在溶胶层,也被称为“纤毛周围”层或“气道表面液体”,纤毛进行摆动和舒张。润滑性的溶胶层使存在于纤毛顶端的凝胶状黏液能够通过纤毛细胞的纤毛摆动进行运输。由于采样困难,关于溶胶层的物理和生化特性知之甚少。凝胶层由与蛋白质和脂质相连的高分子量糖蛋白(黏蛋白)组成。它们形成了一个含水量高(95%)的凝胶网络,其流变学和物理特性(黏弹性、黏附性)在正常情况下可适应保护气道黏膜,特别是通过黏液纤毛运输来实现。黏液的黏附特性受其脂质组成和水合程度的影响,对于通过纤毛活动和咳嗽控制黏液运输的效率非常重要。最佳的黏液纤毛运输需要中等的黏度和弹性。在阻塞性气道疾病中,无论是遗传性的,如囊性纤维化(CF),还是后天获得性的(急性或慢性支气管炎),特别是在炎症和感染发作期间,黏液脱水与分泌或渗出分子的增加以及DNA含量的显著增加有关。这些异常导致气道分泌物的黏度和黏附性增加,并导致其通过纤毛活动的运输速率异常降低以及咳嗽清除效率低下。鉴于CF气道分泌物的物理和功能特性发生了这些改变,药物治疗方法应旨在使黏液重新水化,并通过刺激氯离子分泌(即使用与氨氯地平联合的UTP或ATP以阻断钠离子和水的重吸收)来恢复正常的黏液纤毛或咳嗽运输。在急性感染发作期间,重组人脱氧核糖核酸酶(rhDNase)可通过改善其流变学特性迅速防止黏液淤滞。通过“表面活性剂”疗法在溶胶相界面润滑黏液也可能是一种非常有前景的治疗方法,以降低气道分泌物的高黏度和高黏附性。

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