Mucin Histochemistry of Tracheal Goblet Cells after Oral Administration of Ambroxol

Vajner L. , V. Konrádová, J . Uhl ík , J . Zocová: Mucin Histochemistry of Tracheal Goblet Cells after Oral Administration of Ambroxol. Acta Vet. Brno 2001, 70: 9-13. Previous studies on the effect of various mucolytic drugs on the tracheal epithelium ultrastructure revealed ambroxol as the most harmful one. To complete these studies, we decided to evaluate the effect of ambroxol on the glycoconjugate content in the secretion of tracheal goblet cells. Using the methods of both conventional and lectin histochemistry, the percentage of tracheal goblet cells containing various glycoconjugates was evaluated. Twenty minutes after oral administration of 7.5 mg of ambroxol, goblet cells containing neutral glycoconjugates disappeared from the rabbit tracheal epithelium. Among goblet cells containing acidic glycoconjugates, the percentage of sialylated glycoconjugate-containing ones slightly decreased compared with control healthy rabbits. Oral administration of ambroxol only slightly affected the composition of glycoconjugates contained in goblet cells of the tracheal epithelium in rabbits. Tracheal goblet cells, conventional and lectin histochemistry, mucolytic drug ambroxol, rabbit Ambroxol, the most frequently used mucolytic agent in clinical practice, affects both ciliated and secretory cells in the respiratory system. It stimulates ciliary activity as well as incorporation of precursors into phospholipids in granular pneumocytes causing thus a decrement of mucus adhesion to the hypophase. According to pharmacological studies, it facilitates incorporation of hydrolytic enzymes into lysosomes of the airways’ secretory cells. Activation of these acidic mucopolysaccharide-degrading enzymes leads to a decrease of the sputum viscosity (·míd and Holcát 1994). In our previous studies, reactions of the rabbit tracheal epithelium to oral administration of a single therapeutic dose of 6 various mucolytic drugs were compared. The adverse effect of ambroxol was the most pronounced (Konrádová et al. 1985ab; 1996a). More than ninety seven per cent of the goblet cells had been stimulated to discharge their mucus. They either released their secretion from apical granules and/or detached packets of granules (14.5%) or were completely evacuated (83%) and only remnants of their degenerated cytoplasm were left in the epithelium. On the other hand, the cells of the rabbit terminal bronchiole revealed only mild signs of pathological alteration after oral administration of ambroxol and the secretory activity of Clara cells did not differ from that found in controls (Uhlík et al. in press). Lamb and Reid (1972) and Damyanov (1987) deduced a common tendency to the decrease of sialylated glycoconjugates and the increase of sulphated ones as the reaction to any alteration of the tracheal epithelium. To complete the study, changes of the glycoconjugate content of the tracheal goblet cells were studied under the same experimental conditions using both conventional and lectin histochemistry. ACTA VET. BRNO 2001, 70: 9–13 Address for correspondence: MVDr. Ludûk Vajner, CSc., Charles University, 2nd Medical Faculty Institute of Histology and Embryology V úvalu 84, 150 06 Praha 5 Motol, Czech Republic Phone: +420 2 2443 5982 Fax: +420 2 2443 5820 E-mail: [email protected] http://www.vfu.cz/acta-vet/actavet.htm Materials and Methods Seven SPF New Zealand White male rabbits (Charles River, Sulzfeld, Germany) of the average body weight 2219 ± 484 g were used. Three of them were orally given 1 ml of Mucosolvan sol. (Boehringer Ingelheim International GmbH, Ingelheim, Germany), i.e. a dose routinely used in infants of the age up to one year. This volume contained 7.5 mg of ambroxol (2-amino-3,5-dibromo-N-[trans-4 hydroxy cyclohexyl] benzylamine). The material was collected under general anaesthesia (ketamine 35 mg/kg and xylazine 5 mg/kg intramuscularly) and local subcutaneous infiltration of the ventral cervical field with procaine, 20 min post exposure. Four rabbits served as untreated healthy controls, the material was collected immediately after the induction of anaesthesia. The experimental procedures were approved by the Animals Protection Expert Commission of the Faculty. The middle portions of tracheae between the 15th and 20th tracheal rings were sampled. The formalin-fixed samples were processed by the routine paraffin-embedding method. Serial sections 5-7 μm thick were made. The combined staining method of Alcian Blue at pH 2.5 (AB 2.5) followed by PAS-reaction according to Mowry and Winkler (1956) was used to reveal both total acidic and neutral glycoconjugates. Selective staining of acidic sulphated glycoconjugates was obtained using Alcian Blue at pH 1.0 (AB 1) (Kiernan 1981). Acidic nonsulphated (sialylated) glycoconjugates were counted as the difference between total acidic and acidic sulphated glycoconjugates. To detect sialylated glycoconjugates directly, the methods of in situ lectin histochemistry were used. At first, we used the Sata’s modification (Sata et al. 1990) of digoxigenin-labelled lectin reaction, visualised by the alkaline phosphatase (AP)-X-phosphate (BCIP)-nitroblue tetrazolium (NBT) system (Boehringer Mannheim Biochemica, Germany). In this study, both Maackia amurensis agglutinin (MAA), detecting terminal N-acetylneuraminic acid (2-3) glycosidically linked to galactose, and Sambucus nigra agglutinin (SNA), detecting terminal N-acetylneuraminic acid α(2-6) glycosidically linked to galactose or N-acetylgalactosamine, were employed. The Tritrichomonas mobilensis lectin (TML) (Calbiochem, La Jolla, USA) possessing the exclusive affinity to various modifications in linkages of both N-acetylneuraminic and N-glycolneuraminic acids was also employed (Babál et al. 1996). After dewaxing and rehydrating, the endogenous AP was blocked (Blocking reagent, Boehringer Mannheim Biochemica, Germany) and sections incubated with TML in the concentration 30 μg/ml for 60 min. The non-specific binding sites to the primary antibody were blocked by 10-min submersion in 5% low-fat milk. Then the sections were incubated with the primary monoclonal antibody against TML (Calbiochem, La Jolla, USA) in the dilution 1:100 for 20 min. As the last step, the secondary polyclonal rabbit antibody against the whole molecule of the mouse IgG, labelled with AP (Sigma-Aldrich Chemie, Deisenhofen, Germany) in the dilution 1:50 for 30 minutes, followed by BCIP-NBT visualisation, was used. Blocking endogenous AP was verified by omitting the first step of the method. Specific lectin binding was verified by 15min incubation of lectins with control substrates transferrin and fetuin preceding the incubation with sections. Only goblet cells containing well-developed granules with the positive reaction were evaluated. Marginal sections of the cells as well as differentiating or empty secretory elements were not included. The absolute numbers of evaluated goblet cells were 398 and 402 in control and treated animals, respectively. For statistical evaluation, relative values of the six categories of goblet cells were evaluated by the chi-square test of homogeneity in frequency tables, using the Yates’ correction in low frequencies when appropriate. The equivalency of sialylated glycoconjugate-detecting methods was tested by the paired t-test, median (sign) test, and Wilcoxon’s paired test.