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首页> 外文期刊>Respiration: International Review of Thoracic Diseases >Physical and functional properties of airway secretions in cystic fibrosis--therapeutic approaches.
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Physical and functional properties of airway secretions in cystic fibrosis--therapeutic approaches.

机译:囊性纤维化中气道分泌物的物理和功能特性-治疗方法。

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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.
机译:呼吸道周围的气道分泌物形成由水“溶胶”层和更表面的“凝胶”层组成的两相层。在溶胶层(也称为“珍珠层”或“气道表面流体”)中,纤毛跳动并松弛。润滑溶胶层使纤毛末端的凝胶粘液能够通过纤毛细胞的纤毛搏动而被运输。由于取样困难,对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连接的高分子量糖蛋白(粘蛋白)组成。它们形成了高含水量(95%)的凝胶网络,其流变和物理特性(粘弹性,黏附性)在正常条件下适应,可以保护气道粘膜,特别是通过粘膜纤毛运输。受其脂质组成和水合程度影响的粘液的黏附特性对于控制通过纤毛活动和咳嗽来控制粘液运输的功效非常重要。为了获得最佳的粘膜纤毛运输,需要中等的粘度和弹性。在阻塞性气道疾病中,无论是遗传性原因,例如囊性纤维化(CF)还是后天性疾病(急性或慢性支气管炎),尤其是在炎症和感染性发作期间,粘液脱水都会导致分泌或渗出分子的增加,并伴有明显的DNA含量的增加。这些异常导致气道分泌物的粘度和粘附性增加,并且是由于它们通过睫毛活动而异常低的转运速度和无效的咳嗽清除的原因。考虑到CF气道分泌物的物理和功能特性的这些变化,药理学方法应旨在通过刺激氯离子分泌(例如,使用UTP或ATP与amiloride联用,以阻断粘液水化并恢复正常的粘膜纤毛或咳嗽运输)。在感染的急性发作期间,重组人DNase(rhDNase)可能会通过改善其流变性而迅速预防粘液淤积。通过“表面活性剂”疗法对溶胶相界面处的粘液进行润滑也可以代表减少气道分泌物的高粘度和高粘附性的非常有前途的治疗方法。

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