期刊论文详细信息
Journal of Neuroinflammation
The antiprotozoal drug pentamidine ameliorates experimentally induced acute colitis in mice
Luca Steardo1  Rosario Cuomo2  Carla Cirillo3  Caterina Scuderi1  Giovanni Sarnelli2  Elena Capoccia1  Giuseppe Esposito1 
[1] Department of Physiology and Pharmacology ‘Vittorio Erspamer’, University SAPIENZA of Rome, P. le Aldo Moro 5, 00185, Rome, Italy;Department of Clinical and Experimental Medicine, University of Naples FEDERICO II, Via S. Pansini 5, 80131, Naples, Italy;Current address: Laboratory for Enteric NeuroScience (LENS), TARGID, KU Leuven, Herestraat 49, 3000, Leuven, Belgium
关键词: Enteric glia;    S100B protein;    Acute colitis;    Pentamidine;   
Others  :  1160096
DOI  :  10.1186/1742-2094-9-277
 received in 2012-09-26, accepted in 2012-11-19,  发布年份 2012
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【 摘 要 】

Background

Intestinal inflammation is partly driven by enteroglial-derived S100B protein. The antiprotozoal drug pentamidine directly blocks S100B activity. We aimed to investigate the effect of pentamidine on intestinal inflammation using an animal model of dextran sodium sulphate (DSS)-induced acute colitis.

Methods

Mice were divided into: control group, colitis group (4% DSS for four days) and two pentamidine-treated colitis groups (0.8 mg/kg and 4 mg/kg). Anti-inflammatory effect of pentamidine was assessed in colonic tissue by evaluating the disease activity index and the severity of histological changes. Colonic tissue were also used to evaluate cyclooxigenase-2, inducible nitric oxide synthase, S100B, glial fibrillary acidic protein, phosphorylated-p38 MAPkinase, p50, p65 protein expression, malondyaldheyde production, mieloperoxidase activity, and macrophage infiltration. Nitric oxide, prostaglandin E2, interleukin-1 beta, tumor necrosis factor alpha, and S100B levels were detected in plasma samples. Parallel measurements were performed in vitro on dissected mucosa and longitudinal muscle myenteric plexus (LMMP) preparations after challenge with LPS + DSS or exogenous S100B protein in the presence or absence of pentamidine.

Results

Pentamidine treatment significantly ameliorated the severity of acute colitis in mice, as showed by macroscopic evaluation and histological/biochemical assays in colonic tissues and in plasma. Pentamidine effect on inflammatory mediators was almost completely abrogated in dissected mucosa but not in LMMP.

Conclusions

Pentamidine exerts a marked anti-inflammatory effect in a mice model of acute colitis, likely targeting S100B activity. Pentamidine might be an innovative molecule to broaden pharmacological tools against colitis.

【 授权许可】

   
2012 Esposito et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Monteleone G, Pallone F, MacDonald TT: Emerging immunological targets in inflammatory bowel disease. Curr Opin Pharmacol 2011, 11:640-645.
  • [2]Helper DJ, Rex DK: Inflammatory bowel disease. Endoscopy 2001, 33:140-146.
  • [3]Reinders CI, Herulf M, Ljung T, Hollenberg J, Weitzberg E, Lundberg JO, Hellström PM: Rectal mucosal nitric oxide in differentiation of inflammatory bowel disease and irritable bowel syndrome. Clin Gastroenterol Hepatol 2005, 3:777-783.
  • [4]Hendel J, Nielsen OH: Expression of cyclooxygenase-2 mRNA in active inflammatory bowel disease. Am J Gastroenterol 1997, 92:1170-1173.
  • [5]Ruhl A, Nasser Y, Sharkey KA: Enteric glia. Neurogastroenterol Motil 2004, 16:44-49.
  • [6]Cirillo C, Sarnelli G, Esposito G, Turco F, Steardo L, Cuomo R: S100B protein in the gut: the evidence for enteroglial-sustained intestinal inflammation. World J Gastroenterol 2011, 17:1261-1266.
  • [7]Collins SM, Bercik P: The relationship between intestinal microbiota and the central nervous system in normal gastrointestinal function and disease. Gastroenterology 2009, 136:2003-2014.
  • [8]De Filippis D, Esposito G, Cirillo C, Cipriano M, De Winter BY, Scuderi C, Sarnelli G, Cuomo R, Steardo L, De Man JG, Iuvone T: Cannabidiol reduces intestinal inflammation through the control of neuroimmune axis. PLoS One 2011, 6:e28159.
  • [9]Cirillo C, Sarnelli G, Esposito G, Grosso M, Petruzzelli R, Izzo P, Calì G, D'Armiento FP, Rocco A, Nardone G, Iuvone T, Steardo L, Cuomo R: Increased mucosal nitric oxide production in ulcerative colitis is mediated in part by the enteroglial-derived S100B protein. Neurogastroenterol Motil 2009, 21:1209-e112.
  • [10]von Boyen GB, Schulte N, Pflüger C, Spaniol U, Hartmann C, Steinkamp M: Distribution of enteric glia and GDNF during gut inflammation. BMC Gastroenterol 2011, 11:3. BioMed Central Full Text
  • [11]Cirillo C, Sarnelli G, Turco F, Mango A, Grosso M, Aprea G, Masone S, Cuomo R: Proinflammatory stimuli activates human-derived enteroglial cells and induces autocrine nitric oxide production. Neurogastroenterol Motil 2011, 23:e372-e382.
  • [12]Esposito G, Cirillo C, Sarnelli G, De Filippis D, D'Armiento FP, Rocco A, Nardone G, Petruzzelli R, Grosso M, Izzo P, Iuvone T, Cuomo R: Enteric glial-derived S100B protein stimulates nitric oxide production in celiac disease. Gastroenterology 2007, 133:918-925.
  • [13]Adami C, Bianchi R, Pula G, Donato R: S100B-stimulated NO production by BV-2 microglia is independent of RAGE transducing activity but dependent on RAGE extracellular domain. Biochim Biophys Acta 2004, 1742:169-177.
  • [14]Hofmann MA, Drury S, Fu C, Qu W, Taguchi A, Lu Y, Avila C, Kambham N, Bierhaus A, Nawroth P, Neurath MF, Slattery T, Beach D, McClary J, Nagashima M, Morser J, Stern D, Schmidt AM: RAGE mediates a novel proinflammatory axis: a central cell surface receptor for S100/calgranulin polypeptides. Cell 1999, 97:889-901.
  • [15]Schmidt AM, Yan SD, Yan SF, Stern DM: The multiligand receptor RAGE as a progression factor amplifying immune and inflammatory responses. J Clin Invest 2001, 108:949-955.
  • [16]Pearson RD, Hewlett EL: Pentamidine for the treatment of Pneumocystis carinii pneumonia and other protozoal diseases. Ann Intern Med 1985, 103:782-786.
  • [17]Charpentier TH, Wilder PT, Liriano MA, Varney KM, Pozharski E, MacKerell AD Jr, Coop A, Toth EA, Weber DJ: Divalent metal ion complexes of S100B in the absence and presence of pentamidine. J Mol Biol 2008, 382:56-73.
  • [18]Park MY, Ji GE, Sung MK: Dietary kaempferol suppresses inflammation of dextran sulfate sodium-induced colitis in mice. Dig Dis Sci 2012, 57:355-363.
  • [19]Cooper HS, Murthy SN, Shah RS, Sedergran DJ: Clinicopathologic study of dextran sulfate sodium experimental murine colitis. Lab Invest 1993, 69:238-249.
  • [20]Di Rosa M, Radomski M, Carnuccio R, Moncada S: Glucocorticoids inhibit the induction of nitric oxide synthase in macrophages. Biochem Biophys Res Commun 1990, 172:1246-1252.
  • [21]Thoree V, Skepper J, Deere H, Pele LC, Thompson RP, Powell JJ: Phenotype of exogenous microparticle-containing pigment cells of the human Peyer's patch in inflamed and normal ileum. Inflamm Res 2008, 57:374-378.
  • [22]Mullane KM, Kraemer R, Smith B: Myeloperoxidase activity as a quantitative assessment of neutrophil infiltration into ischemic myocardium. J Pharmacol Methods 1985, 14:157-167.
  • [23]Mihara M, Uchiyama M: Determination of malonaldehyde precursor in tissues by thiobarbituric acid test. Anal Biochem 1978, 86:271-278.
  • [24]Kindt S, Vanden Berghe P, Boesmans W, Roosen L, Tack J: Prolonged IL-1beta exposure alters neurotransmitter and electrically induced Ca(2+) responses in the myenteric plexus. Neurogastroenterol Motil 2010, 22:321-e85.
  • [25]Ford AC, Bernstein CN, Khan KJ, Abreu MT, Marshall JK, Talley NJ, Moayyedi P: Glucocorticosteroid therapy in inflammatory bowel disease: systematic review and meta-analysis. Am J Gastroenterol 2011, 106:590-599.
  • [26]Ford AC, Achkar JP, Khan KJ, Moayyedi P: Efficacy of 5-aminosalicylates in ulcerative colitis: systematic review and meta-analysis. Am J Gastroenterol 2011, 106:601-616.
  • [27]Cottone M, Renna S, Modesto I, Orlando A: Is 5-ASA still the treatment of choice for ulcerative colitis? Curr Drug Targets 2011, 12:1396-1405.
  • [28]Rutgeerts P, Vermeire S, Van Assche G: Biological therapies for inflammatory bowel diseases. Gastroenterology 2009, 136:1182-1197.
  • [29]Fok KC, Ng WW, Henderson CJ, Connor SJ: Cutaneous sarcoidosis in a patient with ulcerative colitis on infliximab. J Crohns Colitis 2012, 6:708-712.
  • [30]Kinnunen U, Färkkilä M, Mäkisalo H: A case report: Ulcerative colitis, treatment with an antibody against tumor necrosis factor (infliximab), and subsequent liver necrosis. J Crohns Colitis 2012, 6:724-727.
  • [31]Huang X, Lv B, Jin HF, Zhang S: A meta-analysis of the therapeutic effects of tumor necrosis factor-α blockers on ulcerative colitis. Eur J Clin Pharmacol 2011, 67:759-766.
  • [32]von Boyen GB, Steinkamp M, Reinshagen M, Schäfer KH, Adler G, Kirsch J: Proinflammatory cytokines increase glial fibrillary acidic protein expression in enteric glia. Gut 2004, 53:222-228.
  • [33]Esposito G, De Filippis D, Cirillo C, Sarnelli G, Cuomo R, Iuvone T: The astroglial-derived S100beta protein stimulates the expression of nitric oxide synthase in rodent macrophages through p38 MAP kinase activation. Life Sci 2006, 78:2707-2715.
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