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The effect of polymyxin B and some mast-cell constituents on mucosal mast cells in the duodenum of the rat

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Summary

Mucosal mast cells in the rat duodenum show no morphological signs of exocytosis of granules and do not release histamine after treatment with polymyxin B in doses large enough to cause almost complete degranulation of connective-tissue mast cells of tongue, skin, and mesentery with concomitant release of ∼ 60% of the tissue histamine. Administration of polymyxin B in gradually increasing doses over a period of 5ds resulted in a statistically significant increase in mucosal mast cells and a comparable increase in duodenal histamine content, whereas the connective-tissue mast cells in the other tissues examined became fewer in number, the remaining cells showing profound morphological changes, and tissue histamine levels, were reduced to ∼ 40% of the controls. A similar increase in mucosal mast cells has been observed after treatment with another mast-cell secretagogue, compound 48/80. This suggests that the increase in mucosal mast cells may be an indirect effect of these compounds, related to their activation of other mast cells and mediated by material(s) secreted by the connective-tissue mast cells. Possible mediators such as heparin, histamine, and 5-hydroxytryptamine injected for 5 ds in doses large enough to account for the amount released from the degranulated mast cells had no effect on the morphology or numbers of mast cells in any of the tissues examined.

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References

  • Andén N-E, Magnusson T (1967) An improved method for fluorometric determination of 5-hydroxytryptamine in tissues. Acta Physiol Scand 69:87–94

    Google Scholar 

  • Bertler Å, Carlsson A, Rosengren E (1958) A method for the fluorometric determination of adrenalin and noradrenalin in tissues. Acta Physiol Scand 44:273–292

    Google Scholar 

  • Bhatt KGS, Jalota R, Sanyal RK (1964) Action of various drugs on the tissue histamine and 5-hydroxytryptamine content of common laboratory animals. Indian J med Res 52:52

    Google Scholar 

  • Bloom GD, Haegermark Ö (1965) A study on morphological changes and histamine release by Compound 48/80 in rat peritoneal mast cell. Exp Cell Res 40:637–654

    Google Scholar 

  • Enerbäck L (1966a) Mast cells in rat gastrointestinal mucosa. 1. Effects of fixation. Acta Pathol Microbiol Scand 66:289–302

    Google Scholar 

  • Enerbäck L (1966b) Mast cells in rat gastrointestinal mucosa. 2. Dye-binding and metachromatic properties. Acta Pathol Microbiol Scand 66:303–312

    Google Scholar 

  • Enerbäck L (1966c) Mast cells in rat gastrointestinal mucosa. 3. Reactivity towards Compound 48/80. Acta Pathol Microbiol Scand 66:313–322

    Google Scholar 

  • Enerbäck L (1966d) Mast cells in rat gastrointestinal mucosa. 4. Monoamine storing capacity. Acta Pathol Microbiol Scand 67:365–369

    Google Scholar 

  • Enerbäck L, Löwhagen GB (1979) Long term increase in mucosal mast cells in rat induced by administration of Compound 48/80. Cell Tissue Res 198:209–215

    Google Scholar 

  • Enerbäck L, Wingren U (1980) Histamine content of peritoneal and tissue mast cells of growing rats. Histochemistry 66:113–124

    Google Scholar 

  • Fawcett DW (1954) Cytological and pharmacological observations on the release of histamine by mast cells. J Exp Med 100:217–224

    Google Scholar 

  • Goth A, Johnson AR (1975) Current concepts on the secretory function of mast cells. Life Sci 16:1201–1214

    Google Scholar 

  • Green H, Erickson RW (1964) Effect of some drugs upon rat brain histamine content. Int J Neuropharmacol 3:315–329

    Google Scholar 

  • Gustafsson B, Enerbäck L (1980) A cytofluorometric analysis of polymer-induced mast cell secretion. Exp Cell Biol 48:15–30

    Google Scholar 

  • Horner AA (1971) Macromolecular heparin from rat skin. J Biol Chem 246:231–239

    Google Scholar 

  • Horner AA (1974) Demonstration of endogenous heparin in rat blood. Adv Exp Med Biol 52:85–93

    Google Scholar 

  • Jarret EE, Bazin H (1974) Elevation of total serum IgE in rats following helminth parasite infection. Nature 251:613–614

    Google Scholar 

  • Kremzner E, Wilson I (1961) A procedure for determination of histamine. Biochem Biophys Acta 50:364–367

    Google Scholar 

  • Lagunoff D (1972a) Contributions of electron microscopy to the study of mast cells. J Invest Dermatol 58:296–311

    Google Scholar 

  • Lagunoff D (1972b) The mechanism of histamine release from mast cells. Biochem Pharmacol 21: 1889–1896

    Google Scholar 

  • Lagunoff D (1973) Membrane fusion during mast cell secretion. J Cell Biol 57:252–259

    Google Scholar 

  • Mota K, Beraldo WT, Junqueira LCU (1953) Protamine-like property of compound 48/80 and Stilbamidine and their action on mast cells. Proc Sco Exp Biol (NY) 83:455–457

    Google Scholar 

  • Miller HRP (1971) Immune reaction in mucous membranes. II. The differentiation of intestinal mast cells during helminth expulsion in the rat. Lab Invest 24:339–347

    Google Scholar 

  • Miller HRP, Walshaw R (1972) Immune reactions in mucous membranes. IV. Histochemistry of intestinal mast cells during helminth expulsion in the rat. Am J Pathol 69:195–206

    Google Scholar 

  • Murray M, Miller HRP, Jarret FH (1968) The globule leucocyte and its derivation from the subepithelial mast cells. Lab Invest 19:222–234

    Google Scholar 

  • Parrat JR, West GB (1957) Release of 5-hydroxytryptamine and histamine from tissues of the rat. J Physiol (Lond) 137:179–192

    Google Scholar 

  • Paton WDM (1951) Compound 48/80: A potent histamine liberator. Br J Pharmacol 6:499–508

    Google Scholar 

  • Riley JF, West GB (1955) Tissue mast cells. Studies with a histamine-liberator of low toxicity (Compound 48/80). J Pathol Bacteriol 69:269–282

    Google Scholar 

  • Röhlich P, Andersson P, Uvnäs B (1971) Electron microscopic observations on Compound 48/80-induced degranulation in rat mast cells. J Cell Biol 51:465–483

    Google Scholar 

  • Shore PA, Burkhalter A, Cohn VH (1959) A method for the fluorometric assay of histamine in tissues. J Pharmacol Exp Ther 127:182–186

    Google Scholar 

  • Wilcoxon F (1947) Probability tables for individual comparisons by ranking methods. Biometrics 3:119–122

    Google Scholar 

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Supported by grants from the Swedish Medical Research Council, Project no 2235

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Enerbäck, L., Löwhagen, G., Löwhagen, O. et al. The effect of polymyxin B and some mast-cell constituents on mucosal mast cells in the duodenum of the rat. Cell Tissue Res. 214, 239–246 (1981). https://doi.org/10.1007/BF00249208

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