The ultrastructure of the epithelium of terminal bronchioles in rabbits was studied 40 minutes after intratracheal administration of iodinated water-soluble non-ionic contrast agent iopamidol. The signs of pathological alteration of the epithelial cells may be a result of the transitional hypoxia during administration. The secretory Clara cells were not stimulated to release their secretion, nor the signs of epithelial cells' proliferation were noticed.
Terminal bronchioles, rabbit, ultrastructure, colltrast agents, tracheobronchographyIn spite of an extensive development of non-invasive radiological techniques, the tracheobronchography remains irreplaceable diagnostic method visualising the airways. In our previous study, we aimed at finding the most suitable contrast agent from the morphological point of view evaluating the degree of damage to the airway epithelium. In experiment, the ultrastructure of the epithelium of large extrapulmonary airways was thoroughly studied shortly after intratracheal administration of three iodinated water-soluble contrast agents (iopamidol, iohexol and Na-meglumine ioxaglate) (Konnidova et al. 1990(Konnidova et al. , 1995. The administration of iopamidol caused only mild damage to the tracheal epithelium, while the degree of injury of this epithelium due to administration of other two agents was classified as moderate to severe. After iopamidol administration, the regeneration was not completed in the course of two days (Konnldova et al. 1996). Recently, the light microscopic study of the rabbits' airways after iohexol tracheobronchography showed relatively severe inflammatory and even necrotic changes in the area of the mucous membrane (Thompson et al. 1997). Therefore, we decided to extend our studies and to investigate also the reaction of the epithelium in terminal bronchioles to this diagnostic procedure.
Materials and MethodsSix clinically healthy rabbits (males, body weight 1,740 g -3,800 g) were used. Under general anaesthesia (ketamine 35 mg/kg and xylazine 5 mg/kg intramuscularly), we cannulated the tracheae of three of them and injected 0.5 ml of iopamidol (N,N' -bis(2-hydroxy-l-hydroxy-methyl-ethyl)-2.4,6-triiodo-5-lactamidoisophthalamide) (IOPAMIRO 300, Bracco, Milan, Italy) into their airways under the X-ray control (Plate III., Fig. I). The animals breathed regularly and did not show any signs of breathlessness. Forty minutes post exposure, the thorax was opened and lungs were removed. The lung better filled with the contrast agent was immediately perfused by 5% glutaraldehyde in O.IM cacodylate buffer (pH 7.2) and one of the lobes was transversely sectioned. Tiny pieces of the tissue were collected, fixed for 90 minutes with the same fixative and then for 60 minutes with 2% OS04 in the same buffer (pH 7.4). The material was dehydrated in graded series of alcohol and embedded in a Durcupan-Epon mixture. Terminal bronchioles were localised in semithin sections stained with toluidine blue.