Abstract
The respiratory burst and subsequent production of oxygen radicals and metabolites by the leukocyte are considered important contributing processes in nonspecific microbicidal systems.1 In addition, in disease states in which inflammation, tissue destruction, and the apparent absence of bacterial invasion are predominant features, excessive and inappropriate production of oxygen radicals and metabolites is thought to play a substantial role in continuing tissue destruction.2 Despite a lack of substantial direct evidence for a primary role, there is nonetheless much indirect evidence incriminating oxygen metabolites as playing a major contributing role in inflammation.2 Oxygen radicals have been strongly implicated as pathogenic in a wide variety of inflammatory disease states involving most physiological organ systems.3
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References
Babior BM, Kipnes RS, Curnutte JT: Biological defense mechanisms: The production by leukocytes of superoxide, a potential bactericidal agent. J Clin Invest 52: 741–744, 1973.
McCord JM, Wong K: Phagocyte-produced free radicals: Roles in cytotoxicity and inflammation, in Oxygen-Free Radicals and Tissue Damage. CIBA Foundation Symposium 65, Amsterdam, Elsevier, 1979, pp. 343–369.
Fantone JC, Ward PA: Role of oxygen-derived free radicals and metabolites in leukocyte-dependent inflammatory reactions. Am J Pathol 107: 395–418, 1982.
Singal PK, Kapur N, Dhillon KS: Role of free radicals in catecholamine-induced cardiomyopathy. Can J Physiol Pharmacol 60: 1390–1397, 1982.
Donaldson J, McGregor D, La Bella F: Manganese neurotoxicity: A model for free radical-mediated neurodegeneration. Can J Physiol Pharmacol 9: 443–445, 1982.
Lunec J, Halloran SP, White RA, et al: Free radical oxidation peroxidation) products in serum and synovial fluid in rheumatoid arthritis. J Rheumatol 8: 233–245, 1981.
McCord JM: Free radicals and inflammation: Protection of synovial fluid by superoxide dismutase. Science 185: 529–531, 1974.
Hyrst NP, Bessac B, Nuki G: Monocyte superoxide anion production in rheumatoid arthritis: Preliminary evidence for enhanced rates of superoxide anion production by monocytes from patients receiving penicillamine, sodium aminothiomalate and corticosteroids. Ann Rheum Dis 43: 28–33.
Schalkwijk J, van den Berg WB1, van, de Putte LB A et al: Hydrogen peroxide suppresses the proteoglycan synthesis of intact articular cartilage. J Rheumatol 12: 205–210, 1985.
Weiss SJ, Lampert MB, Test ST: Long-lived oxidants generated by human neutrophils: Characterization and bioactivity. Science 222: 625–628, 1985.
Weiss SJ, Pepping G, Ortiz X, et al: Oxidative autoactivation of latent collagenase by human neutrophils. Science 227: 747–749, 1985.
Babior BM: The respiratory burst of phagocytes. J Clin Invest 73: 599–601, 1984.
Lewis DA: Endogenous anti-inflammatory factors. Biochem Pharmacol 33: 1705–1714, 1984.
Menander-Huber KB: Double blind controlled clinical trials in man with bovine copper zinc superoxide dismutase (orgotein), in Bannister WH, Bannister JV (eds): Biological and Clinical Aspects of Superoxide and Superoxide Dismutase. Amsterdam, Elsevier/North-Holland, 1980, pp. 408–423.
Koyrounakis LH, Yiangou M: Bee venom and adjuvant-induced disease. (Letter.) J Rheumatol 10: 522, 1983.
Chang YH, Bliven ML: Antiarthritic effect of bee venom. Agents Actions 9: 205–211, 1979.
McCord JM, Wong K, Stokes SH, et al: Superoxide and inflammation: A mechanism for the antiinflammatory activity of superoxide dismutase. Acta Physiol Scand 4 (suppl) 94: 25–30, 1980.
Flower R, Blackwell AJ: Anti-inflammatory steroids induce biosynthesis of a phospholipase A2 inhibitor which prevents prostaglandin generation. Nature (Lond) 278: 456–459, 1979.
Hirata F, Schiffmann E, Venkatasubramanian K, et al: A phospholipase A2 inhibitory protein in rabbit neutrophils induced by glucocorticoids. Proc Natl Acad Sci USA 77: 2533–2536, 1980.
Travis J, Johnson D: Human alphaj protease inhibitor. Methods Enzymol 80: 754–765, 1981.
Clark RA, Stone PJ, Haga GD, et al: Myeloperoxidase-catalysed inactivation of alphaj-protease inhibitor by human neutrophils. J Biol Chem 256: 3348–3353, 1981.
Cochrane CG: Plasma proteins and inflammatory disease. Pharmacol Rev 340: 39–42, 1982.
Kitagawa S, Takaki F, Sakamota S: Serine protease inhibitors inhibit superoxide production by human basophils stimulated by anti-IgE. Biochem Biophys Res Commun 95: 801–806, 1980.
Kitagawa S, Takai F, Sakamoto S: Evidence that proteases are involved in superoxide production by human polymorphonuclear leukocytes and monocytes. J Clin Invest 65: 74–81, 1980.
Kitagawa S, Takai F, Sakamoto S: Possible involvement of proteases in superoxide production by human polymorphonuclear leukocytes. (Letter.) FEBS Lett 99: 275–282, 1979.
Bird J, Mohd-Hidir S, Lewis DA: Putrescine—A potent endogenous anti-inflammatory substance in inflammatory exudates. Agents Actions 13: 348–353, 1983.
Qi DF, Schatzman RC, Mazzei GJ, et al: Polyamines inhibit phospholipid-sensitive and calmodulin- sensitive Ca2 + -dependent protein kinases. Biochem J 281: 281–288, 1983.
Porter R, O’Connor (eds): Substance P in the Nervous System. CIBA Foundation Symposium 91. London, 1982.
Hartung HP, Toyka KV: Activation of macrophages by substance P. Induction of oxidative burst and thromboxane release. Eur J Pharmacol 89: 301–305, 1983.
Hartung HP, Walters K, Toyka KV: Substance P binding properties and studies on cellular responses in guinea pig macrophages. J Immunol 136: 3856–3863, 1986.
Paton JC, Ferrante A: Inhibition of human polymorphonuclear leukocytes respiratory burst, bactericidal activity and migration by pneumolysin. Infect Immun 41: 1212–1216, 1983.
Johnson MK, Geoffroy C, Alouf JE: Binding of cholesterol by sulfhydryl-activated cytolysins. Infect Immun 27: 97–101, 1980.
Anderson BR, Duncan JL: Activation of human neutrophil metabolism by streptolysin O. J Infect Dis 141: 680–685.
Cavalieri SJ, Snyder IS: Effect of E. Coli alpha-hemolysin on human peripheral leucocyte function in vitro. Infect Immun 37: 966–974, 1982.
Gemmell CJ, Peterson PM, Schmelling DG, et al: Effect of staphylococcal alpha-toxin on phagocytosis of staphylococci by human polymorphonuclear leucocytes. Infect Immun 38: 975–980, 1982.
Remaley AT, Kuhns BD, Basford RE, et al: Leishmania phosphatase blocks neutrophil 02 production. J Biol Chem 259: 11173–11175, 1984.
Saha AK, Dowling JD, La Marco K, et al: Properties of an acid phosphatase from Legionella micdadei which blocks superoxide anion production by human neutrophils. Arch Biochem Biophys 243: 150–160, 1985.
Somerfield SD: Bee venom and arthritis. NZ Med J 99: 281–283, 1986.
Somerfield SD, Stach JL. Mraz C, et al: Bee venom melittin blocks neutrophil 02 production. Inflammation 10:175–182, 1986
Takeshige K, Minakami S: Involvement of calmodulin in phagocytic respiratory burst of leukocytes. Biochem Biophys Res Commun 99: 484–490, 1981.
Comte M, Maulet Y, Cox JA: Ca2+-dependent high-affinity complex formation between calmodulin and melittin. Biochem J 209: 269–272, 1983.
Kato N, Raynor RL, Wise BC, et al: Inhibition by melittin of phospholipid-sensitive and calmodu- lin-sensitive Ca2 + -dependent protein kinases. Biochem J 202: 217–224, 1982.
Malencik DA, Anderson SG: Binding of hormones and neuropeptides by calmodulin. Biochemistry 22: 1995–2001, 1983.
Cox JA, Comte M, Fitton JE, et al: The interaction of calmodulin with amphiphilic peptides. J Biol Chem 260: 2527–2534, 1985.
Blumenthal DK, Takio K, Eldman A, et al: Identification of the calmodulin-binding domain of skeletal muscle light chain kinase. Proc Natl Acad Sci USA 82: 3187–3191, 1985.
Archer CB, Page CP, Paul W, et al: Inflammatory characteristics of platelet activating factor (PAF) in human skin. Br J Dermatol 110: 45–50, 1984.
Camussi G, Palowski I, Teita C, et al: Acute lung inflammation induced in the rabbit by local instillation of l-C-octadectyl-2-acetyl-.M-glyceryl-3 phosphorylcholine or of native platelet-activat- ing factor. Am J Pathol 112: 78–88, 1983.
Gay JC, Beckman JK, Zaboy KA: Modulation of neutrophil oxidative responses to soluble stimuli by PAF. Blood 67: 931–936, 1986.
Kirtley ME, McKay M: Fructose-1,6-biphosphate, a regulator of metabolism. Mol Cell Biochem 18: 141–149, 1977.
Schinetti ML, Lazzarino G: Inhibition of phorbol ester stimulated chemiluminescence and superox-ide production in human neutrophils by fructose 1-6-diphosphate. Biochem Pharmacol 35:1762– 1764, 1986.
Badwey JA, Karnovsky ML: Production of superoxide and hydrogen peroxide by an NADH-oxidase in guinea pig polymorphonuclear leukocytes. J Biol Chem 254: 11530–11537, 1979.
Babior BM, Peters WA: The 02-producing enzyme of human neutrophils. J Biol Chem 256:2321– 2323, 1981.
Cronstein BN, Kramer SB, Weissmann G, et al: Adenosine: A physiological modulator of superox-ide anion generation by human neutrophils. J Exp Med 158: 1160–1177, 1983.
Sattin BN, Rail TW: The effect of adenosine and adenine nucleotides on the cyclic adenosine 3’,5’- phosphate content of guinea pig cerebral cortex slices. Mol Pharmacol 6: 13–23, 1970.
Van Calker D, Muller M, Hamprecht B: Adenosine regulates via two different types of receptors, the accumulation of cyclic AMP in cultured brain cells. J Neurochem 33: 999–1005, 1979.
Cronstein BN, Kramer SB, Rosenstein ED, et al: Adenosine modulates the generation of superoxide anion by stimulated human neutrophils via interaction with a specific cell surface receptor. Ann NY Acad Sci 451: 291–301, 1985.
Pike MC, Snyderman R: Transmethylation reactions regulate affinity and functional activity of chemostatic factor receptors on macrophages. Cell 28: 107–114, 1982.
Harrell RA, Cianciolo GJ, Copeland TD, et al: Suppression of the respiratory burst of human monocytes by a synthetic peptide homologous to envelope proteins of human and animal retro-viruses. J Immunol 136: 3517–3520, 1986.
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© 1988 Plenum Press, New York
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Somerfield, S.D., Skamene, E. (1988). Modulation of the Respiratory Burst by Naturally Occurring Substances. In: Sbarra, A.J., Strauss, R.R. (eds) The Respiratory Burst and Its Physiological Significance. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-5496-3_9
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DOI: https://doi.org/10.1007/978-1-4684-5496-3_9
Publisher Name: Springer, Boston, MA
Print ISBN: 978-1-4684-5498-7
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