The Effect of Intravenously Administered Acetylcholine on the Glycoconjugate Composition in Goblet Cells of the Tracheal Epithelium in Rabbits

Vajner L. , J . Uhl ík , V. Konrádová, J . Zocová: The Effect of Intravenously Administered Acetylcholine on the Glycoconjugate Composition in Goblet Cells of the Tracheal Epithelium in Rabbits. Acta Vet. Brno 2000, 69: 17-23. To evaluate the influence of cholinergic stimulation on the composition of glycoconjugates in goblet cells, we studied the tracheal epithelium of rabbits 5 minutes and 20 minutes after i.v. administration of acetylcholine in doses 0.1 mg and 0.5 mg, respectively. Using both conventional and lectin histochemistry, we compared the percentage of tracheal goblet cells containing neutral glycoconjugates to those containing total acidic glycoconjugates, sulphated acidic glycoconjugates, and sialylated acidic glycoconjugates. A conspicuous increase in percentage of neutral glycoconjugates-containing goblet cells and a decrease of sialylated glycoconjugatescontaining goblet cells occurred as early as 5 minutes after the administration of the lower dose and were recorded 20 minutes post exposure, too. Five minutes post exposure, the higher dose evoked a decrease in percentage of both neutraland sialylated glycoconjugates-containing goblet cells. Twenty minutes after the administration of the higher dose, percentage of all studied elements reached values similar to those found in the lower dose group. The cholinergic stimulation did not cause total disappearance of both neutraland sialylated glycoconjugates-containing goblet cells. Only the reaction of goblet cells 5 minutes after the administration of the higher acetylcholine dose differed quantitatively from the reactions in remaining experimental groups. Airways’ epithelium, cholinergic stimulation, glycoconjugates, lectin histochemistry In our previous studies, we demonstrated that the goblet cells (GC) in the rabbit tracheal epithelium were overstimulated and damaged due to the intravenous (i.v.) administration of acetylcholine. An apocrine type of secretion and also chain exocytosis were found after the administration of both doses of acetylcholine. Twenty minutes after the administration of 0.5 mg of acetylcholine, the degeneration of GC evoked massive differentiation of new secretory elements (Konrádová et al. 1996ab). Similar reaction of GC was also described by Specian and Neutra (1980) in the tissue culture of intestinal GC, and by Newman et al. (1996) in the tracheal epithelium of guinea pigs. Tokuyama et al. (1990) and Fung et al. (1992) confirmed the stimulating effect of vagal control to the secretion of airways’ GC and submucosal glands. Ramnarine and Rogers (1994) stressed non-adrenergic, non-cholinergic (NANC) neural mechanisms, coworking with neurogenic acetylcholine as “the secretion fine tuning”. A direct effect of acetylcholine on tracheal secretory elements was further confirmed as a dose-dependent in studies by Kamijo et al. (1993), Woods et al. (1996), and Matera et al. (1998). Miyata et al. (1998) doubted the acetylcholine role in controlling production of high molecular weight-glycoconjugates in spite of the study by Steel and Hanrahan (1997) on GC of the tracheal epithelium in hamsters. The presence of neutral and acidic sulphated and acidic sialylated glycoconjugates ACTA VET. BRNO 2000, 69: 17–23 Address for correspondence: MVDr. Ludûk Vajner, CSc. Institute of Histology and Embryology 2nd Medical Faculty, Charles University V úvalu 84, 150 06 Praha 5-Motol, Czech Republic Phone: +420 2 2443 5982 (1) Fax: +420 2 2443 5820 E-mail: [email protected] http://www.vfu.cz/acta-vet/actavet.htm (GCCs) was widely evidenced in many species including humans (Lamb and Reid 1972; Jones and Reid 1978; Jacob and Poddar 1982; Spicer et al. 1983; Castel ls et al. 1990, 1991, 1992, 1994; Jeffery et al. 1992; Kim et al. 1997). Damjanov (1987) stressed the differences in the GCC composition among individual species. Jones and Reid (1978) and Jeffery et al. (1992) described the conspicuous increase up to total dominance of acidic sulphated GCCs in patients suffering from cystic fibrosis and bronchitis. Lamb and Reid (1972) and Damjanov (1987) held the decrease of acidic sialylated GCCs and the increase of acidic sulphated ones for a common reaction of the tracheal epithelium to general alteration. Miyata et al. (1998) described the protective effects of sialic acids on the airways’ epithelium. To complete our previous studies, we decided to study also the effect of i.v. administered acetylcholine on the composition of the mucus secreted by GC in the tracheal epithelium of rabbits. Materials and Methods In experiment, we used 16 SPF New Zealand White male rabbits (Charles River, Germany) of the average body weight 1,758 ± 146 g. Four healthy rabbits served as untreated controls. The remaining animals were divided in two groups of six rabbits and were treated intravenously with 0.1 mg and 0.5 mg of acetylcholine (Ciba, Niederwangen, Belgium), respectively. All experimental procedures were performed in animals under general anaesthesia using the i.m. administration of a mixture of ketamine and xylazine according to the certification of the Animals Protection Expert Commission of the Faculty. The middle portions of tracheae between the 15th and 20th tracheal rings were sampled. The material was collected 5 and 20 minutes post exposure, respectively. 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 (AB) at pH 2.5 followed by PAS-reaction according to Mowry and Winkler (1956) was used to reveal both total acidic and neutral GCCs. Selective staining of acidic sulphated GCCs was obtained using AB at pH 1.0 (Kiernan 1981). To detect sialylated GCCs 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 Nacetylneuraminic acid (2-3) glycosidically linked to galactose, and Sambucus nigra (SNA) agglutinin, detecting terminal N-acetylneuraminic acid (2-6) glycosidically linked to galactose or N-acetylgalactosamine, were employed. The Tritrichomonas mobilensis lectin (TML) possessing the exclusive affinity to various modifications in linkages of both N-acetylneuraminic and N-glycolneuraminic acids was also used (Babál et al. 1994, 1995, 1996ab). We modified the original Babál’s method. After dewaxing and rehydrating, the endogenous AP was blocked 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-minute submersion in 5% low-fat milk. Then the sections were incubated with the primary monoclonal antibody against TML, the supernatant fluid of the hybridoma culture (mouse-myeloma cell line P3-X63, clone B-VI-10C4) in the dilution 1:2. 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 15-minute incubation of lectins with control substrates transferrin and fetuin, preceding the incubation with sections. We evaluated only goblet cells containing well-developed granules with the positive reaction in each method used. The granules had to fill at least 2/3 of the height of the epithelium. In each animal, at least 100 goblet cells were evaluated using all given methods. For statistical evaluation, relative values of the six categories of GC, revealed by individual methods, were evaluated by the χ2 test of homogeneity in frequency tables, using the Yates’ correction in low frequencies, and by the F-test.