Restoration of mucociliary transport in the fluid-depleted trachea by surface-active instillates

被引:21
作者
Ballard, ST
Parker, JC
Hamm, CR
机构
[1] Univ S Alabama, Dept Physiol, Coll Med, Mobile, AL 36688 USA
[2] Univ S Alabama, Dept Pediat, Coll Med, Mobile, AL 36688 USA
关键词
airway surface liquid; cystic fibrosis; mucociliary transport; pigs; surfactants;
D O I
10.1165/rcmb.2005-0214OC
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Severe impairment of mucociliary transport (MCT) is a hallmark of cystic fibrosis (CF) lung disease. Recent studies demonstrate that pharmacologic inhibition of anion and liquid secretion in pig tracheas modelsthe MCT defect in CF through depletion of the periciliary fluid component of airway surface liquid. In the present study, the effectiveness of various aqueous instillates on rehydration of the airway surface and restoration of MCT was assessed in this model. Excised porcine tracheas were mounted in a chamber that permitted simultaneous measurement of MCT and adventitial exposure of the airways to Krebs solution. When anion and liquid secretion were inhibited by treatment with bumetanide and dimethylamiloride, MCT was greatly reduced. Luminal instillation of aqueous solutions containing surface-active substances (1 % Tween8O or calfactant) transiently restored MCT to high rates in nearly all tissues. Mucosal treatment with only Krebs solution or hypertonic saline restored MCT in only one half of the tracheas. We conclude that aqueous salt solutions alone can hydrate airway surfaces and restore MCT in some tissues, but surface-active substances may provide additional benefit in restoring MCT in this model of mucociliary stasis. We speculate that administration of surface-active substances, by aerosol or lavage, might help to restore MCT in the airways of patients with CF.
引用
收藏
页码:500 / 504
页数:5
相关论文
共 30 条
  • [1] ALLEGRA L, 1985, EUR J RESPIR DIS S, V142, P71
  • [2] DEMONSTRATION THAT CFTR IS A CHLORIDE CHANNEL BY ALTERATION OF ITS ANION SELECTIVITY
    ANDERSON, MP
    GREGORY, RJ
    THOMPSON, S
    SOUZA, DW
    PAUL, S
    MULLIGAN, RC
    SMITH, AE
    WELSH, MJ
    [J]. SCIENCE, 1991, 253 (5016) : 202 - 205
  • [3] Anzueto A, 1997, JAMA-J AM MED ASSOC, V278, P1426
  • [4] Nasal mucociliary transport and ciliary ultrastructure in cystic fibrosis. A comparative study with healthy volunteers
    Armengot, M
    Escribano, A
    Carda, C
    Sanchez, C
    Romero, C
    Basterra, J
    [J]. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 1997, 40 (01) : 27 - 34
  • [5] CFTR involvement in chloride, bicarbonate, and liquid secretion by airway submucosal glands
    Ballard, ST
    Trout, L
    Bebök, Z
    Sorscher, EJ
    Crews, A
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1999, 277 (04) : L694 - L699
  • [6] Liquid secretion inhibitors reduce mucociliary transport in glandular airways
    Ballard, ST
    Trout, L
    Mehta, A
    Inglis, SK
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2002, 283 (02) : L329 - L335
  • [7] BALLARD ST, 2003, PEDIAT PULMONOL, P209
  • [8] Surface hydrophobicity is increased in the ileum and proximal colon of cystic fibrosis mice
    Chung, C
    van Hoof, L
    Policova, Z
    Beharry, S
    Sherman, PM
    Neumann, AW
    Durie, P
    [J]. PEDIATRIC RESEARCH, 1999, 46 (02) : 174 - 178
  • [9] COLTEN HR, 1991, HARRISONS PRINCIPLES, P1072
  • [10] DEBENTZMANN SG, 1993, EUR RESPIR J, V6, P1156