Abstract
Glucocorticoid hormones (GC) are essential in all aspects of human health and disease. Their anti-inflammatory and immunosuppressive properties are reasons for therapeutic application in several diseases. GC suppress immune activation and uncontrolled overproduction and release of cytokines. GC inhibit the release of pro-inflammatory cytokines and stimulate the production of anti-inflammatory cytokines. Investigation of GC’s mechanism of action, suggested that polyamines (PA) may act as mediators or messengers of their effects. Beside glucocorticoids, spermine (Spm) is one of endogenous inhibitors of cytokine production. There are many similarities in the metabolic actions of GC and PA. The major mechanism of GC effects involves the regulation of gene expression. PA are essential for maintaining higher order organization of chromatin in vivo. Spermidine and Spm stabilize chromatin and nuclear enzymes, due to their ability to form complexes with negatively charged groups on DNA, RNA and proteins. Also, there is an increasing body of evidence that GC and PA change the chromatin structure especially through acetylation and deacetylation of histones. GC display potent immunomodulatory activities, including the ability to induce T and B lymphocyte apoptosis, mediated via production of reactive oxygen species (ROS) in the mitochondrial pathway. The by-products of PA catabolic pathways (hydrogen peroxide, amino aldehydes, acrolein) produce ROS, well-known cytotoxic agents involved in programmed cell death (PCD) or apoptosis. This review is an attempt in the better understanding of relation between GC and PA, naturally occurring compounds of all eukaryotic cells, anti-inflammatory and apoptotic agents in physiological and pathological conditions connected to oxidative stress or PCD.
Similar content being viewed by others
References
Abbott AC, Bird CC (1983) Cytolethal sensitivity of human lymphoid cells to glucocorticoids and oxidized polyamines. Biochem Biophys Res Commun 115:737–742
Auphan N, Di Donato JA, Rosette C, Helmberg A, Karin M (1995) Immunosuppression by glucocorticoids: inhibition of NF-κB activity through induction of IκB synthesis. Science 270:286–290
Babbar N, Gerner EW, Casero RA (2006a) Induction of spermidine/spermine N1-acetyltransferase (SSAT) by aspirin in Caco-2 colon cancer cells. Biochem J 394:317–324
Babbar N, Amy Hacker A, Huang Y, Casero RA (2006b) Tumor necrosis factor α induces spermidine/spermine N1-acetyltransferase through nuclear factor κB in non-small cell lung cancer cells. J Biol Chem 281(34):24182–24192
Babbar N, Murray-Stewart T, Casero RA (2007) Inflammation and polyamine catabolism: the good, the bad and the ugly. Biochem Soc Trans 35:300–304
Bachrach U (2004) Polyamines and cancer. Amino Acids 26:307–309
Baldwin AS (1996) The NF-κB and IκB proteins: new discoveries and insights. Annu Rev Immunol 14:649–683
Barnes PJ (1998) Editorial review: anti-inflammatory actions of glucocorticoids: molecular mechanisms. Clin Sci 94:557–572
Barnes PJ (2006) Corticosteroids: the drugs to beat. Eur J Pharmacol 533(1–3):2–14
Barnes PJ, Adcock IM (1993) Anti-inflammatory actions of steroids: molecular mechanisms. Trends Pharmacol Sci 14:436–441
Bauer PM, Fukuto JM, Buga GM, Pegg AE, Ignarro LJ (1999) Nitric oxide inhibits ornithine decarboxylase by S-nitrosylation. Biochem Biophys Res Commun 262:355–358
Bauer PM, Buga GM, Fukuto JM, Pegg AE, Louis J, Ignarro LJ (2001) Nitric oxide inhibits ornithine decarboxylase via S-nitrosylation of cysteine 360 in the active site of the enzyme. J Biol Chem 276(37):34458–34464
Baxter JD, Rousseau GG (1979) Glucocorticoid hormone action. Monogr Endocrinol 12:1–24
Beaven MA. Intracellular signaling section. http://www.dir.nhlbi.nih.gov/labs/lmi/ics/
Bernardi P, Scorrano L, Colonna R, Petronilli V, Di Lisa F (1999) Mitochondria and cell death. Mechanistic aspects and methodological issues. Eur J Biochem 264:687–701
Bishop BP, Young J, Peng T, Richards JF (1985) An inhibitor of ornithine decarboxylase in thymus and spleen of dexamethasone-treated rats. Biochem J 226:105–112
Bjelakovic G, Pavlovic D (1987) Effect of pyridoxine on the polyamine oxidase activity in the liver and spleen of dexamethasone-treated guinea-pigs. Yugosl Physiol Pharmacol Acta 24:249–256 (Serbian)
Bjelakovic G, Pavlovic D, Stojanovic I, Jevtovic T, Nikolic J, Kocic G (2006) Effects of glucocorticoids on polyamine metabolism in liver and spleen of guinea pig during sensitization. Amino Acids 31:457–462
Bonneau MJ, Poulin R (2000) Spermine oxidation leads to necrosis with plasma membrane phosphatidylserine redistribution in mouse leukemia cells. Exp Cell Res 259(1):23–34
Boumpas DT (1972) A novel action of glucocorticoids—NF kappaB inhibition. Br J Rheumatol 35(8):709–710
Boumpas DT, Chrousos GP, Wilder RL, Cupps TR, Balow JE (1993) Glucocorticoid therapy for immune-mediated diseases: basic and clinical correlates. Ann Intern Med 119(12):1198–1208
Brune B, Hartzell P, Nicotera P, Orrenius S (1991) Spermine prevents endonuclease activation and apoptosis in thymocytes. Exp Cell Res 195:323–329
Bursch W, Ellinger A, Gerner CH, Frohwein U, Schulte-Hermann R (2000) Programmed cell death (PCD): apoptosis, autophagic PCD, or others? An NY Acad Sci 926:1–12
Choi W, Proctor L, Xia Q, Feng Y, Gerner EW, Chiao PJ, Hamilton SR, Zhang W (2006) Inactivation of IkappaB contributes to transcriptional activation of spermidine/spermine N(1)-acetyltransferase. Mol Carcinog 45(9):685–693
Chrousos PG (1995) The hypothalamic–pituitary–adrenal axis and immune-mediated inflammation. N Engl J Med 332(20):1351–1363
Cifone MG, Migliorati G, Parroni R, Marchetti C, Millimaggi D, Santoni A, Riccardi C (1999) Dexamethasone-induced thymocyte apoptosis: apoptotic signal involves the sequential activation of phosphoinositide-specific phospholipase C, acidic sphingomyelinase, and caspases. Blood 93(7):2282–2296
Cohen JJ (1993) Programmed cell death and apoptosis in lymphocyte development and function. Chest 103(2 Suppl):99S–101S
Cohen SS (1998) A guide to the polyamines. 1-543 Oxford University Press, New York
Colombatto S, Fasulo L, Grillo MA (1988) Polyamines in rat liver during experimental inflammation. Agents Actions 24(3–4):326–330
Cosío BG, Torrego A, Adcock IM (2005) Molecular mechanisms of glucocorticoids. Arch Bronchoneumol 41:34–41
D’Agostino L, Di Luccia A (2002) Polyamines interact with DNA as molecular aggregates. Eur J Biochem 269:4317–4325
Dalla Via L, Di Noto V, Toninello A (1999) Binding of spermidine and putrescine to energized liver mitochondria. Arch Biochem Biophys 365(2):231–238
Dash P (2005) Apoptosis. Basic Medical Sciences, St George’s, University of London (http://www.sgul.ac.uk/depts/immunology/~dash)
Dash PR, Cartwright JE, GStJ Whitley (2003) Nitric oxide inhibits polyamine-induced apoptosis in the human extravillous trophoblast cell line SGHPL-4. Hum Reprod 18(5):959–968
Datta RK, Sen S, Ghosh JJ (1969) Effect of polyamines on the stability of brain-cortex ribosomes. Biochem J 114:847–854
De Bosscher K, Vanden Berghe W, Haegeman G (2003) The interplay between the glucocorticoid receptor and nuclear factor κB or activator protein-1: molecular mechanisms for gene repression. Endocr Rev 24(4):488–522
Demonacos C, Djordjevic-Markovic R, Tsawdaroglou N, Sekeris CE (1995) The mitochondrion as a primary site of action of glucocorticoids: the interaction of the glucocorticoid receptor with mitochondrial DNA sequences showing partial similarity to the nuclear glucocorticoid responsive elements. J Steroid Biochem Mol Biol 55(1):43–55
Deng W, Viar MJ, Johnson LR (2005) Polyamine depletion inhibits irradiation-induced apoptosis in intestinal epithelia. Am J Physiol Gastrointest Liver Physiol 289:G599–G606
Deroo BJ, Archer TK (2001a) Glucocorticoid receptor activation of the IκBα promoter within chromatin. Mol Biol Cell 12(11):3365–3374
Deroo BJ, Archer TK (2001b) Glucocorticoid receptor-mediated chromatin remodeling in vivo. Oncogene 20:3039–3046
Desiderio MA, Stefano Mattei S, Biondi G, Colombo MP (1993) Cytosolic and nuclear spermidine acetyltransferases in growing NIH 3T3 fibroblasts stimulated with serum or polyamines: relationship to polyamine-biosynthetic decarboxylases and histone acetyltransferase. Biochem J 293:475–479
Desiderio MA, Grassilli E, Bellesia E, Salomoni P, Franceschi C (1995) Involvement of ornithine decarboxylase and polyamines in glucocorticoid-induced apoptosis of rat thymocytes. Cell Growth Differ 6:505–513
Desiderio MA, Pogliaghi G, Dansi P (1998) Regulation of spermidine/spermine N1-acetyltransferase expression by cytokines and polyamines in human hepatocarcinoma cells (HepG2). J Cell Physiol 174:125–134
Díaz-Guerra MJM, Velasco M, Martin-Sanz P, Bosca L (1997) Nuclear factor κB is required for the transcriptional control of type II NO synthase in regenerating liver. Biochem J 326:791–797
Distelhorst CW (2002) Recent insights into the mechanism of glucocorticosteroid induced apoptosis. Cell Death Differ 9:6–19
Duma D, Jewell CM, Cidlowski AJ (2006) Multiple glucocorticoid receptor isoforms and mechanisms of post-translational modification. J Steroid Biochem Mol Biol 102(1–5):11–21
Elenkov IJ, Chrousos GP (2002) Stress hormones, proinflammatory and anti-inflammatory cytokines, and autoimmunity. Ann NY Acad Sci 966:290–303
Erez O, Goldstaub D, Friedman J, Kahana C (2002) Putrescine activates oxidative stress dependent apoptotic death in ornithine decarboxylase overproducing mouse myeloma cells. Exp Cell Res 281:148–156
Fadeel B, Orrenius S, Zhivotovsky B (1999) Apoptosis in human disease: a new skin for the old ceremony? Biochem Biophys Res Commun 266:699–717
Ferioli EM, Pinottia O, Pironaa L (1999) Polyamine oxidase activity in lymphoid tissues of glucocorticoid-treated rats. Biochem Pharmacol 58(12):1907–1914
Ferioli ME, Pirona L, Pinotti O (2000) Prolactin and polyamine catabolism: specific effect on polyamine oxidase activity in rat thymus. Mol Cell Endocrinol 165(1–2):51–56
Ferrante A (1985) Inhibition of human neutrophil locomotion by the polyamine oxidase–polyamine system. Immunology 54:785–790
Franchimont D (2004) Overview of the actions of glucocorticoids on the immune response: a good model to characterize new pathways of immunosuppression for new treatment strategies. Ann NY Acad Sci 1024:124–137
Fraser AV, Woster PM, Wallace HM (2002) Induction of apoptosis in human leukemic cells by IPENSpermine, a novel polyamine analogue and anti-metabolite. Biochem J 367:307–312
Goulding NJ (2004) The molecular complexity of glucocorticoid actions in inflammation—a four-ring circus. Curr Opin Pharmacol 4(6):629–636
Green DR, Reed JC (1998) Mitochondria and apoptosis. Science 281:1309–1312
Ha HC, Sirisoma SN, Kuppusamy P, Zweier JL, Patrick M, Woster PM, Casero RA (1998) The natural polyamine spermine functions directly as a free radical scavenger. Proc Natl Acad Sci USA 95(19):11140–11145
Heby O (1981) Role of polyamines in the control cell proliferation and differentiation. Differentiation 19:1–20
Heby O, Persson L (1990) Molecular genetics of polyamine synthesis in eukaryotic cells. Trends Biochem Sci 15:152–158
Hegardt C (2000) On the role of polyamines in apoptosis Avhandling. Dissertation, Lund University
Hegardt C, Andersson G, Oredson SM (2000) Changes in polyamine metabolism during glucocorticoid-induced programmed cell death in mouse thymus. Cell Biol Int 24(12):871–880
Hegardt C, Andersson G, Oredsson SM (2001) Different roles of spermine in glucocorticoid- and Fas-induced apoptosis. Exp Cell Res 266(2):333–341
Hegardt C, Andersson G, Oredsson SM (2003) Spermine prevents cytochrome c release in glucocorticoid-induced apoptosis in mouse thymocytes. Cell Biol Int 27(2):115–121
Herold JMJ, McPherson KG, Reichardt HM (2006) Glucocorticoids in T cell apoptosis and function. Cell Mol Life Sci 63:60–72
Hirsch JG, Dubos RJ (1952) The effect of spermine on tubercle bacilli. J Exp Med 95:191–208
Hobbs CA, Gilmour SK (2000) High levels of intracellular polyamines promote histone acetyltransferase activity resulting in chromatin hyperacetylation. J Cell Biochem 77:345–360
Hogg N, Kalyanaraman B, Joseph J, Struck A, Parthasarathy S (1993) Inhibition of low density lipoprotein oxidation by nitric oxide. Potential role in atherogenesis. FEBS Lett 334:170–174
Hölttä E (1977) Oxidation of spermidine and spermine in rat liver: purification and properties of polyamine oxidase. Biochemistry 16:91–100
Hoshino K, Momiyama E, Yoshida K, Nishimura K, Sakai S, Toida T, Kashiwagi K, Igarashi K (2005) Polyamine transport by mammalian cells and mitochondria: role of antizyme and glycosaminoglycans. J Biol Chem 280(52):42801–42808
Ientile R, De Luca G, Di Giorgio MR, Macaione S (1988) Glucocorticoid regulation of spermidine acetylation in the rat brain. J Neurochem 51(3):677–682
Igarashi K, Kashiwagi K (2000) Polyamines: mysterious modulators of cellular functions. Biochem Biophys Res Commun 271(3):559–564
Igarashi K, Kashiwagi K (2006) Polyamine modulation in Escherichia coli: genes involved in the stimulation of cell growth by polyamines. J Biochem 139(1):11–16
Iuchi T, Akaike M, Mitsui T, Ohshima Y, Shintani Y, Azuma H, Matsumoto T (2003) Glucocorticoid excess induces superoxide production in vascular endothelial cells and elicits vascular endothelial. Circ Res 92:81–89
Janne J, Alhonen L, Leinonen P (1991) Polyamines: from molecular biology to clinical application. Ann Med 23:241–259
Jänne J, Alhonen L, Pietilä M, Keinänen TA (2004) Genetic approaches to the cellular functions of polyamines in mammals. Eur J Biochem 271:877–894
Johnson RM (2005) Polyamines, their biochemistry and role in neoplasia. Proc West Pharmacol Soc 48:21–23
Kagoshima M, Ito K, Cosio B, Adcock IM (2003) Glucocorticoid suppression of nuclear factor-κB: a role for histone modifications. Biochem Soc Trans 31(1):60–65
Karin M (1998) New twists in gene regulation by glucocorticoid receptor: is DNA binding dispensable? Cell 93(4):487–490
Kelley EE, Wagner B, Buettner G, Burns C (1999) Nitric oxide inhibits iron-induced lipid peroxidation in HL-60 cells. Arch Biochem Biophys 319:402–407
Kepka-Lenhart D, Mistry SK, Wu G, Morris SM (2000) Arginase I: a limiting factor for nitric oxide and polyamine synthesis by activated macrophages? Am J Physiol Regul Integr Comp Physiol 279(6):R2237–R2242
Kerr JF, Wyllie AH, Currie AR (1972) Apoptosis: a basic biological phenomenon with wide-ranging implications in tissue kinetics. Br J Cancer 26(4):239–257
Kim YM, Talanian RV, Billiar TR (1997) Nitric oxide inhibits apoptosis by preventing increases in caspase-3-like activity via two distinct mechanisms. J Biol Chem 272(49):31138–31148
Kishimoto M, Fujiki R, Takezawa S, Sasaki Y, Nakamura T, Yamaoka K, Katigawa H, Kato S (2006) Nuclear receptors mediated gene regulation through chromatin remodeling and histone modifications. Endocrinol J 53(2):157–172
Liao CP, Lasbury ME, Wang SH, Zhang C, Durant PJ, Tschang D, Lee CH (2006) Inflammatory cells are sources of polyamines that induce alveolar macrophage to undergo apoptosis during pneumocystis pneumonia. J Eukaryot Microbiol 53(S1):S134–S135
Lill-Elghanian D, Schwartz K, King L, Fraker P (2002) Glucocorticoid-induced apoptosis in early B cells from human bone marrow. Exp Biol Med 227:763–770
Lim HY, Muller N, Herold MJ, van den Brandt J, Reichardt HM (2007) Glucocorticoids exert opposing effects on macrophage function dependent on their concentration. Immunology 122:47–53
Liu Y, Fiskum G, Schubert D (2002) Generation of reactive oxygen species by the mitochondrial electron transport chain. J Neurochem 80:780–787
Lu NZ, Cidlowski JA (2004) The origin and functions of multiple human glucocorticoid receptor isoforms. Ann NY Acad Sci 1024:102–123
Maccarrone M, Bari MN, Battista N, Di Rienzo M, Falciglia K, Finazzi Agro A (2001) Oxidation products of polyamines induce mitochondrial uncoupling and cytochrome c release. FEBS Lett 507(1):30–34
Maiuri MC, Tajana G, Iuvone T, De Stefano D, Mele G, Ribecco MT, Cinelli MP, Romano MF, Turco MC, Carnuccio R (2004) Nuclear factor-κB regulates inflammatory cell apoptosis and phagocytosis in rat carrageenin-sponge implant model. Am J Pathol 165(1):115–126
Matthews HR (1993) My favorite molecule: polyamines, chromatin structure and transcription. Bio Essays 15(8):561–566
McKay LI, Cidlowski JA (1998) Cross-talk between nuclear factor-κB and the steroid hormone receptors: mechanisms of mutual antagonism. Mol Endocrinol 12(1):45–56
Miller AL, Johnson HB, Medh DR, Townsend MC, Thompson BE (2002) Glucocorticoids and polyamine inhibitors synergize to kill human leukemic CEM cells. Neoplasia 4(1):68–81
Moinard CH, Cynober L, de Bandt JP (2005) Polyamines: metabolism and implications in human diseases. Clin Nutr 24:184–197
Moylan JS, Reid MB (2007) Oxidative stress, chronic diseases, and muscle wasting. Muscle Nerve 35:411–429
Murrray-Stewart T, Wang Y, Devereux W, Robert A, Casero RA (2002) Cloning and characterization of multiple human polyamine oxidase splice variants that code for isoenzymes with different biochemical characteristics. Biochem J 368:673–677
Novac N, Baus D, Dostert A, Heinzel T (2006) Competition between glucocorticoid receptor and NF-κB for control of the human FasL promoter. FASEB J 20:1074–1081
Ott M, Gogvadze V, Zhivotovsky SB (2007) Mitochondria, oxidative stress and cell death. Apoptosis 12:913–922
Oyanagui Y (1984) Anti-inflammatory effects of polyamines in serotonin and carrageenan paw edemata—possible mechanism to increase vascular permeability inhibitory protein level which is regulated by glucocorticoids and superoxide radical. Agents Actions 14(2):228–237
Panagiotidis CA, Artandi S, Calame K, Silverstein SJ (1995) Polyamines alter sequence specific DNA–protein interactions. Nucleic Acids Res 23(10):1800–1809
Papavassiliou AG (1995) Transcription factors. N Engl J Med 332:45–47
Paul-Clark MJ, Roviezzo F, Flower RJ, Cirino G, Del Soldato P, Adcock IM, Perretti M (2003) Glucocorticoid receptor nitration leads to enhanced anti-inflammatory effects of novel steroid ligands. J Immunol 171:3245–3252
Pavlovic DD, Uzunova P, Galabova T, Peneva V, Sokolova Z, Bjelakovic G, Ribarov S (1992) Polyamines as modulators of lipoperoxidation. Gen Physiol Biophys 11(2):203–211
Pegg AE (1986) Recent advances in the biochemistry of polyamines in eukaryotes. Biochem J 234:249–262
Pegg AE (1988) Polyamine metabolism and its importance in neoplastic growth and as a target of chemotherapy. Cancer Res 48:759–774
Pegg AE, Feith DJ (2007) Polyamines and neoplastic growth. Biochem Soc Trans 35:295–299
Pouline R, Pelletier PRG, Pegg AE (1995) Induction of apoptosis by excessive polyamine accumulation in ornithine decarboxylase-overproducing L1210 cells. Biochem J 311:723–727
Pelta J, Livolant F, Sikorav JL (1996) DNA aggregation induced by polyamines and cobalthexamine. J Biol Chem 271(10):5656–5662
Penning LC, Schipper RG, Vercammen D, Verhofstad AAJ, Denecker T, Beyaert R, Vandenabeele P (1998) Sensitization of TNF-induced apoptosis with polyamine synthesis inhibitors in different human and murine tumour cell lines. Cytokine 10(6):423–431
Pfeffer LM, Yang CH, Murt A, McCormack SA, Viar MJ, Ray RM, Johnson LR (2001) Polyamine depletion induces rapid NF-kappa B activation in IEC-6 cells. J Biol Chem 276(49):45909–45913
Pickle S (2005) Glucocorticoid-induced apoptosis: the role of reactive oxygen species and the proteasome. A thesis submitted to the Miami University Honor Program, May, Oxford, Ohio
Pitzalis C, Pipitone N, Perretti M (2002) Regulation of leukocyte–endothelial interactions by glucocorticoids. Ann N Y Acad Sci 966:108–118
Pledgie A, Huang Y, Hacker A, Zhang Z, Woster PM, Davidson NE, Casero RA (2005) Spermine oxidase SMO(PAOh1), not N1-acetylpolyamine oxidase PAO, is the primary source of cytotoxic H2O2 in polyamine analogue-treated human breast cancer cell lines. J Biol Chem 280(48):39843–39851
Ploner C, Schmidt S, Presul E, Renner K, Schrocksnadel K, Rainer J, Riml S, Kofler R (2005) Glucocorticoid-induced apoptosis and glucocorticoid resistance in acute lymphoblastic leukemia. J Steroid Biochem Mol Biol 93:153–160
Pollard KJ, Samuels ML, Crowley KA, Hansen JC, Peterson CL (1999) Functional interaction between GCN5 and polyamines: a new role for core histone acetylation. EMBO J 18(20):5622–5633
Psarra AMG, Solakidi S, Sekeris CE (2006) The mitochondrion as a primary site of action of steroid and thyroid hormones: presence and action of steroid and thyroid hormone receptors in mitochondria of animal cells. Mol Cell Endocrinol 246(1–2):21–33
Que FG, Gores GJ (1996) Cell death by apoptosis: basic concepts and disease relevance for the gastroenterologist. Gastroenterology 110:1238–1243
Ray RM, Viar MJ, Yuan Q, Johnson LR (2000) Polyamine depletion delays apoptosis of rat intestinal epithelial cells. Am J Physiol Cell Physiol 278(3):C480–C489
Rhen T, Cildowski AJ (2005) Anti-inflammatory action of glucocorticoids—new mechanisms for old drugs. N Engl J Med 353(16):1711–1723
Roussel D, Dumas JF, Simard G, Malthiery Y, Ritz P (2004) Kinetics and control of oxidative phosphorylation in rat liver mitochondria after dexamethasone treatment. Biochem J 382:491–499
Salvi M, Toninello A (2004) Effects of polyamines on mitochondrial (Ca2+) transport. Biochim Biophys Acta 1661(2):113–124
Satriano J, Ishizuka S, Archer DC, Blantz RC, Kelly CJ (1999) Regulation of intracellular polyamine biosynthesis and transport by NO and cytokines TNF-α and IFN-γ. Am J Physiol 276(4 Pt 1):C892–C899
Sava IG, Battaglia V, Rossi CA, Salvi M, Toninello A (2006) Free radical scavenging action of the natural polyamine spermine in rat liver mitochondria. Free Radic Biol Med 41(8):1272–1281
Schäcke H, Döcke WD, Asadullah K (2002) Mechanisms involved in the side effects of glucocorticoids. Pharmacol Ther 96(1):23–43
Schäfer SC, Wallerath T, Closs EI, Schmidt C, Schwarz PM, Förstermann U, Lehr HA (2005) Dexamethasone suppresses eNOS and CAT-1 and induces oxidative stress in mouse resistance arterioles. Am J Physiol Heart Circ Physiol 288(1):H436–H444
Schiller M, Blank N, Heyder P, Herrmann M, Gaipl US, Kalden JR, Lorenz HM (2005) Induction of apoptosis by spermine-metabolites in primary human blood cells and various tumor cell lines. Apoptosis 10(5):1151–1162
Schuber F (1989) Influence of polyamines on membrane functions. Biochem J 260:1–10
Seiler N (1995) Polyamine oxidase, properties and functions. Prog Brain Res 106:333–344
Seiler N, Atanassov CL (1994) The natural polyamines and the immune system. Prog Drug Res 43:87–141
Seiler N, Raul F (2005) Polyamines and apoptosis. J Cell Mol Med 9(3):623–642
Shearer JD, Richards JR, Mills CD, Caldwell MD (1997) Differential regulation of macrophage arginine metabolism: a proposed role in wound healing. Am J Physiol 272(35):E181–E190
Sionov RV, Cohen O, Kfir S, Zilberman Y, Yefenof E (2006a) Role of mitochondrial glucocorticoid receptor in glucocorticoid-induced apoptosis. J Exp Med 203(1):189–201
Sionov RV, Kfir S, Zafrir E, Cohen O, Zilberman Y, Yefenof E (2006b) Glucocorticoid-induced apoptosis revisited. A novel role for glucocorticoid receptor translocation to the mitochondria. Cell Cycle 5(10):1017–1026
Soulet D, Rivest S (2003) Polyamines play a critical role in the control innate immune response in the mouse central nervous system. J Cell Biol 162(2):257–268
Southan GJ, Szabo C, Thiemermann C (1994) Inhibition of the induction of nitric oxide synthase by spermine is modulated by aldehyde dehydrogenase. Biochem Biophys Res Comm 203:1638–1644
Stanic I, Facchini A, Borzì RM, Vitellozzi R, Stefanelli C, Goldring MB, Guarnieri C, Facchini A, Flamigni F (2006) Polyamine depletion inhibits apoptosis following blocking of survival pathways in human chondrocytes stimulated by tumor necrosis factor-α. J Cell Physiol 206(1):138–146
Stefanelli C, Bonavita F, Stanic I, Mignani M, Facchini A, Pignatti C, Flamigni F, Caldarera CM (1998) Spermine causes caspase activation in leukaemia cells. FEBS Lett 437(3):233–236
Stefanelli C, Stanic I, Zini M, Bonavita F, Flamigni F, Zambonin L, Landi L, Pignatti C, Guarnieri C, Caldarera CM (2000) Polyamines directly induce release of cytochrome c from heart mitochondria. Biochem J 347(Pt 3):875–880
Struhl K (1998) Histone acetylation and transcriptional regulatory mechanisms. Genes Dev 12(5):599–606
Szabo C, Southan GJ, Wood E, Thiemermann C, Vanne JR (1994a) Inhibition by spermine of the induction of nitric oxide synthase in J774.2 macrophages: requirement of a serum factor. Br J Pharmacol 112(2):355–356
Szabo C, Southan G, Thiemermann C, Vane J (1994b) The mechanism of the inhibitory effect of polyamines on the induction of nitric oxide synthase: role of aldehyde metabolites. Br J Pharmacol 113:757–766
Tabor CW, Tabor H (1984) Polyamines. Annu Rev Biochem 53:749–790
Takao K, Rickhag M, Hegardt C, Oredsson S, Persson L (2006) Induction of apoptotic cell death by putrescine. Int J Biochem Cell Biol 38(4):621–628
Tantini B, Fiumana E, Cetrullo S, Pignatti C, Bonavita F, Shantz LM, Giordano E, Muscari C, Flamigni F, Guarnieri C, Stefanelli C, Caldarera CM (2006) Involvement of polyamines in apoptosis of cardiac myoblasts in a model of simulated ischemia. J Mol Cell Cardiol 40(6):775–782
Thomas T, Thomas JT (2001) Polyamines in cell growth and cell death: molecular mechanisms and therapeutic applications. Cell Mol Life Sci 58:244–258
Thornberry NA, Lazebnik Y (1998) Caspases: enemies within. Science 281:1312–1316
Tomitori H, Usui T, Saeki N, Ueda S, Kase H, Nishimura K, Kashiwagi K, Igarashi K (2005) Polyamine oxidase and acrolein as novel biochemical markers for diagnosis of cerebral stroke. Stroke 36:2609–2616
Toninello A, Dalla Via L, Testa S, Siliprandi D, Siliprandi N (1990) Transport and action of spermine in rat heart mitochondria. Cardioscience 1:287–294
Toninello A, Dalla Via L, Siliprandi D, Garlid KD (1992) Evidence that spermine, spermidine and putrescine are transported electrophoretically in mitochondria by a specific polyamine uniporter. J Biol Chem 267:18393–18397
Toninello A, Salvi M, Mondovi B (2004) Interaction of biologically active amines with mitochondria and their role in the mitochondrial-mediated pathway of apoptosis. Curr Med Chem 11(17):2349–2374
Tonomura N, McLaughlin K, Grimm L, Goldsby RA, Osbourne BA (2003) Glucocorticoid-induced apoptosis of thymocytes: requirement of proteasome-dependent mitchondrial activity. J Immunol 170:2469–2478
Tuckermann JP, Kleiman A, McPherson KG, Reichardt HM (2005) Molecular mechanisms of glucocorticoids in the control of inflammation and lymphocyte apoptosis. Crit Rev Clin Lab Sci 42(1):71–104
Vujcic S, Diegelman P, Bacchi CJ, Kramer DL, Porter CW (2002) Identification and characterization of a novel flavin-containing spermine oxidase of mammalian cell origin. Biochem J 367:665–675
Vujcic S, Liang P, Diegelman P, Kramer DL, Porter CW (2003) Genomic identification and biochemical characterization of the mammalian polyamine oxidase involved in polyamine back-conversion. Biochem J 370:19–28
Wallace HM, Fraser AV (2004) Inhibitors of polyamine metabolism: review article. Amino Acids 26(4):353–365
Wallace HM, Fraser AV, Hughes A (2003) A perspective of polyamine metabolism. Biochem J 376:1–14
Wang Y, Casero RA (2006) Mammalian polyamine catabolism: a therapeutic target, a pathological problem, or both? J Biochem 139(1):17–25
Wang Y, Murray-Stewart T, Devereux W, Hacker A, Frydman B, Woster PM, Casero RA (2003) Properties of purified recombinant human polyamine oxidase, PAOh1/SMO. Biochem Biophys Res Commun 304:605–611
Wang D, Mülle N, Kirsty G, McPherson KG, Reichardt HM (2006) Glucocorticoids engage different signal transduction pathways to induce apoptosis in thymocytes and mature T cells. J Immunol 176:1695–1702
Webb MS, Miller LA, Johnson HB, Fofanov Y, Li T, Wood GT, Thompson EB (2003) Gene networks in glucocorticoid-evoked apoptosis of leukemic cells. J Steroid Biochem Mol Biol 85:183–193
Wei J, Guo H, Gao C, Kuo PC (2004) Peroxide-mediated chromatin remodelling of a nuclear factor κB site in the mouse inducible nitric oxide synthase promoter. Biochem J 377:809–818
Wu C (1997) Chromatin remodeling and the control of gene expression. J Biol Chem 272(45):28171–28174
Yanagawa K, Yamashita T, Yada K, Ohira M, Ishikawa T, Yano Y, Otani S, Sowa M (1998) The antiproliferative effect of HGF on hepatoma cells involves induction of apoptosis with increase in intracellular polyamine concentration levels. Oncol Rep 5:185–190
Yuan Q, Ray RM, Johnson LR (2002) Polyamine depletion prevents camptothecin induced apoptosis by inhibiting the release of cytochrome c. Am J Physiol Cell Physiol 282(6):C1290–C1297
Zhang M, Caragine T, Wang H, Cohen SP, Botchkina G, Soda K, Bianchi M, Ulrich P, Cerami A, Sherry B, Tracey JK (1997) Spermine inhibits proinflammatory cytokine synthesis in human mononuclear cells: a counterregulatory mechanism that restrains the immune response. J Exp Med 185(1):1759–1768
Zhang M, Tracey HW, Kevin J (2000) Regulation of macrophage activation and inflammation by spermine: a new chapter in an old story. Crit Care Med 28(4 Suppl):N60–N66
Zhang W, Ramdas L, Shen W, Song SW, Hu L, Hamilton SR (2003) Apoptotic response to 5-fluorouracil treatment is mediated by reduced polyamines, non-autocrine Fas ligand, and induced tumor necrosis factor receptor. Cancer Biol Ther 2(5):572–578
Zou T, Rao NJ, Guo X, Liu L, Zhang MH, Strauch DE, Bass BL, Wang JY (2004) NF-κB-mediated IAP expression induces resistance of intestinal epithelial cells to apoptosis after polyamine depletion. Am J Physiol Cell Physiol 286:C1009–C1018
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Bjelaković, G., Stojanović, I., Jevtović Stoimenov, T. et al. Metabolic correlations of glucocorticoids and polyamines in inflammation and apoptosis. Amino Acids 39, 29–43 (2010). https://doi.org/10.1007/s00726-010-0489-3
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00726-010-0489-3