AIRWAY MUCUS AND EPITHELIAL FUNCTION IN A CANINE MODEL OF SINGLE-LUNGAUTOTRANSPLANTATION

Citation
Rp. Tomkiewicz et al., AIRWAY MUCUS AND EPITHELIAL FUNCTION IN A CANINE MODEL OF SINGLE-LUNGAUTOTRANSPLANTATION, Chest, 107(1), 1995, pp. 261-265
Citations number
34
Categorie Soggetti
Respiratory System
Journal title
ChestACNP
ISSN journal
00123692
Volume
107
Issue
1
Year of publication
1995
Pages
261 - 265
Database
ISI
SICI code
0012-3692(1995)107:1<261:AMAEFI>2.0.ZU;2-E
Abstract
Impaired mucociliary function following lung transplantation has been reported in several human and animal studies. This could be a result o f altered ciliary function or mucus properties or both. We assessed ai rway epithelial function by means of transepithelial potential differe nce (PD) measurements and physical analysis of mucus. Six mongrel dogs underwent single lung autologous transplantation. Measurements were p erformed preoperatively and 1, 2, 4, and 10 months postoperatively. At 1 and 2 months postoperatively, there was a significant fall in PD fo r the transplanted, left mainstem bronchus only (-13.5+/-1.7 mV at 1 m onth and -14.6+/-1.7 mV at 2 month postoperatively vs -18.6+/-2.3 mV p reoperatively, baseline; p<0.001 for both). The PD values in the small airways, right mainstem bronchus, and the trachea remained unchanged. At 2 months postoperation, the mucus collection rate on the left side was increased (p=0.03), while the mucus viscoelasticity was decreased (p=0.04). By 4 months postoperation, all epithelial parameters had re turned to baseline, and there was no difference in radioaerosol cleara nce between the two lungs. The PD decrease and alterations in secretio n rate and viscoelasticity reflect disturbed epithelial functional int egrity at the site of anastomosis still present at 2 months postoperat ion. Recovery of bronchial epithelial function and clearance in canine studies of lung autotransplantation after healing of the anastomosis area suggest that persistent impairment of lung clearance observed in some long-term human lung transplantation survivors may be due to othe r mechanisms such as impaired healing or epithelial function or both, during immunosuppressive therapy. Mucociliary function in the anastomo sis area is compromised until complete healing ensues; we speculate th at chest physiotherapy may aid in overcoming this obstacle.