Energy metabolism in rat mast cells in relation to histamine secretion
1987; Wiley; Volume: 61; Issue: s2 Linguagem: Inglês
10.1111/j.1600-0773.1987.tb01597.x
ISSN1600-0773
Autores Tópico(s)Amino Acid Enzymes and Metabolism
ResumoPharmacology & ToxicologyVolume 61, Issue s2 p. 1-20 Energy metabolism in rat mast cells in relation to histamine secretion Torben Johansen, Torben Johansen Department of Pharmacology Odense University, Odense DenmarkSearch for more papers by this author Torben Johansen, Torben Johansen Department of Pharmacology Odense University, Odense DenmarkSearch for more papers by this author First published: August 1987 https://doi.org/10.1111/j.1600-0773.1987.tb01597.xCitations: 18AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat References 1 Barger G, Dale HH. Beta-iminazolylethylamine, a depressor constituent of intestinal mucosa. J Physiol (Lond) 1911; 41: 499–503. 2 Riley JF, West GB. The presence of histamine in tissue mast cells. J Physiol (Lond) 1953; 120: 528–37. 3 Hagen P, Barnett RJ, Lee F-L. Biochemical and electron microscopic study of particles isolated from mastocytoma cell. J Pharmacol Exp Ther 1959; 126: 91–108. 4 Lagunoff D. Structural aspects of histamine binding. The mast cell granule. In: US Euler, S Rosell, B Uvnäs, eds. Wenner-Gren Center International Symposium Series 1965; 5: 79–94. 5 Uvnäs B, Thon I-L. A physico-chemical model of histamine release from mast cells. In: US Euler, S Rosell, B Uvnäs, eds. Wenner-Gren Center International Symposium Series 1965; 5: 361–70. 6 Dragstedt CA, Gebauer-Fuelnegg E. Studies in anaphylaxis: I. The appearance of a physiologically active substance during anaphylactic shock. Am J Physiol 1932; 102: 512–9. 7 Parrot JL. Sur la réaction cellulaire de l'anaphylaxie; son caractère aérobic. C R Soc Biol 1942; 136: 361–2. 8 Mongar JL, Schild HO. Inhibition of the anaphylactic reaction. J Physiol (Lond) 1957; 135: 301–19. 8a Mongar JL, Schild HO. Effect of temperature on the anaphylactic reaction. J Physiol (Lond) 1957; 135: 320–338. 9 Chakravarty N. The mechanism of histamine release in anaphylactic reaction in guinea pig and rat. Acta Physiol Scand 1960; 48: 146–66. 10 Moussatché H, Prouvost-Danon A. Influence de l'anaérobiose et de différentes tensions d'oxygène sur la libération d'histamine dans la réaction anaphylactique in vitro. Experientia (Basel) 1960; 16: 118–9. 11 Yamasaki H, Saburo M, Endo K. Energy metabolic aspect of histamine release in anaphylaxis. Jap J Pharmacol 1960; 10: 21–9. 12 Uvnäs B. Mechanism of release from mast cells. Chemotherapia 1961; 3: 137–49. 13 Diamant B, Uvnäs B. Evidence for energy-requiring processes in histamine release and mast cell degranulation in rat tissues induced by compound 48/80. Acta Physiol Scand 1961; 53: 315–29. 14 Rothschild AM, Vugman I, Rocha E Silva M Metabolic studies on the release of histamine by compound 48/80 in the rat diaphragm. Biochem Pharmacol 1961; 7: 248–55. 15 Westerholm B. The influence of anoxia on compound 48/80-induced histamine release from cat skin. Acta Physiol Scand 1960; 50: 300–5. 16 Prouvost-Danon A, Moussatché H. Influence of anaerobic glycolysis on histamine release in the guinea pig and rat anaphylactic reaction in vitro. Nature (Lond) 1961; 192: 361–2. 17 Chakravarty N. Aerobic metabolism in anaphylactic reaction in vitro. Am J Physiol 1962; 203: 1193–8. 18 Boréus LO, Chakravarty N. Tissue mast cells, histamine and slow-reacting substance in anaphylactic reaction in guinea pig. Acta Physiol Scand 1960; 48: 315–22. 19 Mongar JL, Perera BAV. Oxygen consumption of isolated mast cells in the anaphylactic reaction. Nature (Lond) 1964; 202: 93–4. 20 Chakravarty N. Respiration of rat peritoneal mast cells during histamine release induced by antigen-antibody reaction. Exp Cell Res 1968; 49: 160–8. 21 Kahl G-F, Netter KJ. Sauerstoffverbrauch isolierter Peritonealmastzellen der Ratte während der Histaminfreisetzung durch Compound 48/80. Naunyn-Schmiedeberg's Arch Pharmak u Exp Path 1967; 256: 55–63. 22 Moussatché H, Prouvost-Danon A. Influence of sodium succinate and malonate on the histamine release in the anaphylactic reaction in vitro. Arch Biochem Biophys 1958; 77: 108–11. 23 Austen KF, Brocklehurst WD. Enhancement of the anaphylactic release of histamine and slow reacting substance by certain dibasic aliphatic acids and inhibition by monobasic fatty acid. J Exp Med 1961; 113: 541–57. 24 Diamant B, Fredholm B. Effect of glucose and sodium succinate on oxygen uptake and histamine release in rat and guinea-pig lung tissue in vitro. Acta Physiol Scand 1963; 59: 193–8. 25 Moussatché H. Release of histamine in relation to phosphorylation and respiration. In: E Rocha M Silva, ed. Histamine and anti-histaminics. Berlin, Heidelberg, New York: Springer-Verlag, 1966: 645–59. 26 Chakravarty N, Sørensen HJ. Potentiation of anaphylactic histamine release from guinea pig lung by maleate and succinate. Acta Physiol Scand 1973; 88: 401–11. 27 Chakravarty N, Högberg B, Uvnäs B. Mechanism of the release by compound 48/80 of histamine and of a lipid-soluble smooth muscle stimulation principle ("SRS"). Acta Physiol Scand 1959; 45: 255–70. 28 Diamant B. Betydelsen av glycos vid histaminfrisätning och mastcellsdegranulering. Stockholm, 1962. 42 pp. Thesis. 29 Chakravarty N. Glycolysis in rat peritoneal mast cells. J Cell Biol 1965; 25: 123–8. 30 Chakravarty N, Sørensen HJ. Stimulation of glucose metabolism in rat mast cells by antigen, dextran and compound 48/80, used as histamine releasing agents. Acta Physiol Scand 1974; 91: 339–53. 31 Johnson AR, Moran NC. Selective release of histamine from rat mast cells by compound 48/80 and antigen. Am J Physiol 1969; 216: 453–9. 32 Diamant B. Observations on some metabolic enzymes of the mast cell and the macrophage fractions of rat peritoneal cells. Int Arch Allergy 1967; 32: 236–45. 33 Goth A. On the general problem of the release of histamine. In: E Rocha M Silva, ed. Histamine II and anti-histamine. Berlin, Heidelberg, New York: Springer-Verlag, 1978: 57–74. 34 Thon I-L, Uvnäs B. Degranulation and histamine release, two consecutive steps in the release of rat mast cells to compound 48/80. Acta Physiol Scand 1967; 71: 303–15. 35 Bloom GD, Haegermark O. A study on morphological changes and histamine release induced by compound 48/80 in rat peritoneal mast cells. Exp Cell Res 1967; 40: 637–54. 36 Röhlich P, Anderson P, Uvnäs B. Electron microscope observations on compound 48/80-induced degranulation in rat mast cells. Evidence for sequential exocytosis of storage granules. J Cell Biol 1971; 51: 465–83. 37 Lagunoff D. Membrane fusion during mast cell secretion. J Cell Biol 1973; 57: 252–9. 38 Uvnäs B, Åborg C-H, Bergendorff A. Storage of histamine in mast cells. Evidence for an ionic binding of histamine to protein carboxyls in the granule heparin-protein complex. Acta Physiol Scand 1970; 78, Suppl 336: 3–26. 39 Bergendorff A, Uvnäs B. Storage properties of rat mast cell granules in vitro. Acta Physiol Scand 1973; 87: 213–22. 40 Healicon RM, Foreman JC. Receptors for immunoglobulin E (IgE). In: PM Conn, ed. The receptors. Orlando: Academic Press 1984; 1: 83–139. 41 Baltzly R., Buck JS, De Beer EJ, Webb FJ. A family of long-acting depressors. J Amer Chem Soc 1949; 71: 1301–5. 42 Foreman JC, Mongar JL, Gomperts BD. Calcium ionophores and movements of calcium ions following the physiological stimulus to a secretory process. Nature (Lond) 1973; 245: 249–51. 43 Diamant B, Patkar SA. Stimulation and inhibition of histamine release from isolated rat mast cells. Int Archs Allergy appl Immun 1975; 49: 183–207. 44 Johansen T. Mechanism of histamine release from rat mast cells induced by the ionophore A23187: Effects of calcium and temperature. Br J Pharmacol 1978; 63: 643–9. 45 Johansen T. Ethacrynic acid inhibition of histamine release from rat mast cells: Effect on cellular ATP levels and thiol groups. Eur J Pharmacol 1983; 92: 181–9. 46 Johansen T, Chakravarty N. The utilization of adenosine triphosphate in rat mast cells during histamine release induced by anaphylactic reaction and compound 48/80. Naunyn-Schmiedeberg's Arch Pharmacol 1975; 288: 243–60. 47 Johansen T. Adenosine triphosphate levels during anaphylactic histamine release in rat mast cells in vitro. Effects of glycolytic and respiratory inhibitors. Eur J Pharmacol 1979; 58: 107–15. 48 Johansen T. Adenosine triphosphate levels during histamine release induced by compound 48/80 in rat mast cells in vitro. Life Sci 1980; 26: 61–69. 49 Johansen T. Utilization of adenosine triphosphate in rat mast cells during and after secretion of histamine in response to compound 48/80. Acta Pharmacol Toxicol 1983; 53: 245–9. 50 Johansen T. Utilization of adenosine triphosphate in rat mast cells during histamine release induced by the ionophore A23187. Br J Pharmacol 1979; 65: 103–9. 51 Johansen T. Further observations on the utilization of adenosine triphosphate in rat mast cells during histamine release induced by the ionophore A23187. Br J Pharmacol 1980; 69: 657–62. 52 Mongar JL, Schild HO. The effect of calcium and pH on the anaphylactic reaction. J Physiol 1958; 140: 272–84. 53 Foreman JC, Mongar JL. The role of the alkaline earth ions in anaphylactic histamine release. J Physiol 1972; 224: 753–69. 54 Uvnäs B, Thon I-L. Evidence for enzymatic histamine release from isolated rat mast cells. Exp Cell Res 1961; 23: 45–57. 55 Douglas WW, Ueda Y. Mast cell secretion (histamine release) induced by 48/80: calcium-dependent exocytosis inhibited strongly by cytochalasin only when glycolysis is rate-limiting. J Physiol 1973; 324: 97–98P. 56 Kagayama M, Douglas WW. Electron microscope evidence of calcium-induced exocytosis in mast cells treated with 48/80 or the ionophores A-23187 and X-537A. J Cell Biol 1974; 62: 519–26. 57 Cochrane DE, Douglas WW. Calcium-induced extrusion of secretory granules (exocytosis) in mast cells exposed to 48/80 or the ionophores A-23187 and X-537A. Proc Natl Acad Sci USA 1974; 71: 408–12. 58 Johansen T. Calcium requirement in compound 48/80-induced histamine release from rat mast cells in vitro. Life Sci 1980; 27: 369–75. 59 Reed PW, Lardy HA. Antibiotic A23187 as a probe for the study of calcium and magnesium function in biological systems. In: MA Mehlman, RW Hanson eds., The role of membranes in metabolic regulation. New York: Academic Press, 1972: 111–131. 60 Johansen T. Histamine release induced from rat mast cells by the ionophore A23187 in the absence of extracellular calcium. Eur J Pharmacol 1980; 62: 329–34. 61 Payne AN, Garland LG. Interaction between barium, strontium and calcium in histamine release by compound 48/80. Eur J Pharmacol 1978; 52: 329–34. 62 Chakravarty N. The role of plasma membrane Ca++-Mg++ activated adenosine triphosphatase of rat mast cells on histamine release. Acta Pharmacol Toxicol 1980; 47: 223–35. 63 Högberg G, Uvnäs B. Further observations on the disruption of rat mesentery mast cell caused by compound 48/80, antigen-antibody reaction, lecithinase A and decylamine. Acta Physiol Scand 1960; 48: 133–45. 64 Bloom GD, Chakravarty N. Time course of anaphylactic histamine release and morphological changes in rat peritoneal mast cells. Acta Physiol Scand 1970; 78: 410–9. 65 Svendstrup F, Chakravarty N. Glucose metabolism in rat mast cells during histamine release. Exp Cell Res 1977; 106: 223–31. 66 Chan K-F J, Graves DJ. Molecular properties of phosphorylase kinase. In: WY Cheung, ed. Calcium and cell function. Academic Press, Orlando 1984; 5: 1–31. 67 Chakravarty N. Glucose metabolism in rat mast cells. Stimulation of the pentose phosphate pathway by compound 48/80. Agents and Actions 1985; 16: 133–7. 68 Denton RM, McCormack JG. Ca2+ transport by mammalian mitochondria and its role in hormone action. Am J Physiol 1985; 249: E543–E554. 69 McCormack JG, Denton RM. Ca2+ as a second messenger within mitochondria. Trends in Biochem Sci 1986; 11: 258–62. 70 Fiskum G, Lehninger AL. Mitochondrial regulation of intracellular calcium. In: WY Cheung, ed. Calcium and cell function. Academic Press, New York 1982; 2: 39–80. 71 Borle AB. Control, modulation and regulation of cell calcium. Rev Physiol Biochem Pharmacol 1981; 90: 13–153. 72 Rossi CS, Lehninger AL. Stoichiometric relationship between accumulation of ions by mitochondria and the energy-coupling sites in the respiratory chain. Biochem Z 1963; 338: 698–713. 73 Brierley GP, Murer E, Bachmann E. Studies on ion transport. III. The accumulation of calcium and inorganic phosphate by heart mitochondria. Archs Biochem Biophys 1964; 105: 89–102. 74 Bielawski J, Lehninger AL. Stoichiometric relationship in mitochondrial accumulation of calcium and phosphate supported by hydrolysis of adenosine triphosphate. J Biol Chem 1966; 241: 4316–22. 75 Brand MD, Lehninger AL. Superstoichiometric Ca2+ uptake supported by hydrolysis of endogenous ATP in rat liver mitochondria. J Biol Chem 1975; 250: 7958–60. 76 Malmström K, Carafoli E. The interaction of Ca2+ with mitochondria from human myometrium. Archs Biochem Biophys 1977; 182: 657–66. 77 Alexandre A, Reynafarje B, Lehninger AL. Stoichiometry of vectorial H+ movements coupled to electron transport and to ATP synthesis in mitochondria. Proc Natl Acad Sci USA 1978; 75: 5296–5300. 78 Vasington FD, Murphy JV. Ca++ uptake by rat kidney mitochondria and its dependence on respiration and phosphorylation. J Biol Chem 1962; 237: 2670–7. 79 Brierley GP, Murer E, Green DE. Participation of an intermediate of oxidative phosphorylation in ion accumulation by mitochondria. Science, NY 1963; 140: 60–2. 80 Mongar JL, Schild HO. Cellular mechanisms in anaphylaxis. Physiol Rev 1962; 42: 226–70. 81 Yamasaki H. The release of histamine and its mechanism. Proc 17th Jap Med Congr 1967; 555–78. 82 Chakravarty N, Zeuthen E. Respiration of rat peritoneal mast cells. J Cell Biol 1965; 25: 113–21. 83 Shore PA, Burkhalter A, Cohn VH. A method for the fluorometric assay of histamine in tissues. J Pharmacol Exp Ther 1959; 127: 182–6. 84 Bergendorff A, Uvnäs B. Storage of 5-hydroxytryptamine in rat mast cells. Evidence for an ionic binding to carboxyl groups in the granule heparin-protein complex. Acta Physiol Scand 1972; 84: 320–31. 85 McElroy WD. The energy source for bioluminescence in an isolated system. Proc Natl Acad Sci USA 1947; 33: 342–5. 86 Rasmussen H, Nielsen R. An improved analysis of adenosine triphosphate by the luciferase method. Acta Chem Scand 1968; 22: 1745–56. 87 Nielsen R., Rasmussen H. Fractionation of extracts of firefly tails by gel filtration. Acta Chem Scand 1968; 22: 1757–62. 88 Lowry OH, Passonneau JV. A flexible system of enzymatic analysis. New York, London: Academic Press, 1972: 194. 89 Lardy HA, Johnson D, McMurray WC. Antibiotics as tools for metabolic studies I. A survey of toxic antibiotics in respiratory, phosphorylative and glycolytic systems. Arch Biochem 1958; 78: 587–97. 90 Johansen T, Chakravarty N. Dependence of histamine release from rat mast cells on adenosine triphosphate. Naunyn-Schmiedeberg's Arch Pharmacol 1972; 275: 457–63. 91 Johansen T. Dependence of anaphylactic histamine release from rat mast cells on cellular energy metabolism. Eur J Pharmacol 1981; 72: 281–6. 92 Peterson C. Inhibitory action of antimycin A on histamine release from isolated rat mast cells. Acta Pharmacol Toxicol 1974; 34: 347–55. 93 Peterson C. Histamine release induced by compound 48/80 from isolated rat mast cells: Dependence on endogenous ATP. Acta Pharmacol Toxicol 1974; 34: 356–67. 94 Bloom GD, Fredholm B, Haegermark O. Studies on the time course of histamine release and morphological changes induced by histamine liberators in rat peritoneal mast cells. Acta Physiol Scand 1967; 71: 270–82. 95 Bloom GD, Chakravarty N. Time course of anaphylactic histamine release and morphological changes in rat peritoneal mast cells. Acta Physiol Scand 1970; 78: 410–9. 96 Sugiyama K. Calcium-dependent histamine release with degranulation from isolated rat mast cells by adenosine-5′-triphosphate. Jap J Pharmacol 1971; 21: 209–26. 97 Diamant B. The effect of compound 48/80 and distilled water on the adenosine triphosphate content of isolated rat mast cells. Acta Physiol Scand 1967; 71: 283–90. 98 Peterson C, Diamant B. Increased utilization of endogenous ATP in isolated rat mast cells during histamine release induced by compound 48/80. Acta Pharmacol Toxicol 1974; 34: 337–46. 99 Johansen T. Estimation of the rate of energy production of rat mast cells in vitro. Acta Pharmacol Toxicol 1983; 53: 413–6. 100 Diamant B, Lowry OH. Dry weight determination of single lyophilized mast cells of the rat. J Histochem Cytochem 1966; 14: 519–24. 101 Cheung WY. Cyclic 3′,5′-nucleotide phosphodiesterase: demonstration of an activator. Biochem Biophys Res Commun 1970; 38: 533–8. 102 Manalan AS, Klee CB. Calmodulin. In: P Greengard, GA Robison, eds. Advances in cyclic nucleotide and protein phosphorylation research. New York: Raven Press, 1984; 18: 227–78. 103 Klee CB., Newton DL. Calmodulin: An overview. In: JR Parratt, ed. Control and manipulation of calcium movement. New York: Raven Press, 1985: 131–45. 104 De Lorenzo RJ. Calmodulin in neurotransmitter release and synaptic function. Fed Proc 1982; 41: 2265–72. 105 Gagliardino JJ, Harrison DE, Christie MR, Gagliardino EE, Ashcroft SJH. Evidence for the participation of calmodulin in stimulus-secretion coupling in the pancreatic beta-cell. Biochem J 1980; 192: 919–27. 106 Schubart UK, Ehrlichman J, Fleischer N. Regulation of insulin release and protein phosphorylation by calcium and cyclic AMP: possible role of calmodulin. In: WY Cheung, ed. Calcium and cell function. New York, London: Academic Press, 1982; 3: 381–407. 107 Sieghart W, Theoharides TC, Alper SL, Douglas WW, Greengard P. Calcium-dependent protein phosphorylation during secretion by exocytosis in the mast cell. Nature 1978; 275: 329–31. 108 Chakravarty N, Holm Nielsen E. Calmodulin in mast cells and its role in histamine release. Agents and Actions 1985; 16: 122–5. 109 Egsmose C, Bock E, Møllgård K, Thorn NA. Immunocytochemical demonstration of calmodulin in cells secreting by exocytosis. Experientia 1985; 41: 1340–2. 110 Douglas WW, Nemeth EF. On the calcium receptor activating exocytosis: inhibitory effect of calmodulin-interacting drugs on rat mast cells. J Physiol (Lond) 1982; 323: 229–44. 111 Alm PE. Cyclic AMP levels during stimulation and inhibition of histamine release from rat mast cells by the calmodulin inhibitor trifluoperazine. Int Archs Allergy Appl Immunol 1983; 71: 103–11. 112 Peachell PT, Pearce FL. Effect of calmodulin inhibitors on histamine secretion from mast cells. Agents and Actions 1985; 16: 43–4. 113 Hokin MR, Hokin LE. Enzyme secretion and the incorporation of P32 into phospholipids of pancreas slices. J Biol Chem 1953; 203: 967–77. 114 Berridge MJ, Irvine RF. Inositol triphosphate, a novel second messenger in cellular signal transduction. Nature 1984; 312: 315–21. 115 Abdel-Latif AA. Calcium-mobilizing receptors, polyphosphoinositides, and the generation of second messengers. Pharmacol Rev 1986; 38: 227–72. 116 Berridge MJ. Inositol triphosphate and diacylglycerol as second messengers. Biochem J 1984; 220: 345–60. 117 Kennerly DA, Sullivan TJ, Parker CW. Activation of phospholipid metabolism during mediator release from stimulated rat mast cells. J Immunol 1979; 122: 152–9. 118 Cockcroft S, Gomperts BD. Evidence for a role of phosphatidylinositol turnover in stimulus-secretion coupling. Studies with rat peritoneal mast cells. Biochem J 1979; 178: 681–7. 119 Nakamura T, Ui M. Simultaneous inhibition of inositol phospholipid breakdown, arachidonic acid release, and histamine secretion in mast cells by islet-activating protein, pertussis toxin. J Biol Chem 1985; 260: 3584–93. 120 Kennerly DA, Sullivan TJ, Sylwester P, Parker CW. Diacylglycerol metabolism in mast cells: A potential role in membrane fusion and arachidonic acid release. J Exp Med 1979; 150: 1039–44. 121 Ishizuka Y, Imai A, Nakashima S, Nozawa Y. Evidence for de novo synthesis of phosphatidylinositol coupled with histamine release in activated rat mast cells. Biochem Biophys Res Commun 1983; 111: 581–7. 122 Ishizuka Y, Nozawa Y. Concerted stimulation of PI-turnover, Ca2+-influx and histamine release in antigen-activated rat mast cells. Biochem Biophys Res Commun 1983; 117: 710–7. 123 Kikkawa U, Takai Y, Minakuchi R., Inohara S, Nishizuka Y. Calcium-activated phospholipid-dependent protein kinase from rat brain. J Biol Chem 1982; 257: 13341–8. 124 Katakami Y, Kaibuchi K, Sawamura M, Takai Y, Nishizuka Y. Synergistic action of protein kinase C and calcium for histamine release from rat peritoneal mast cells. Biochem Biophys Res Commun 1984; 121: 573–8. 125 Cantwell ME, Foreman JC. Characteristics of the effect of phorbol ester on rat mast cells: interaction with anti-IgE. Agents and Actions 1986; 18: 77–80. Citing Literature Volume61, Issues2August 1987Pages 1-20 ReferencesRelatedInformation
Referência(s)