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Volumn 44, Issue 1, 2014, Pages 17-19

Oxidative stress in cystic fibrosis lung disease: An early event, but worth targeting?

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLCYSTEINE; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; GLUTATHIONE; HYPOCHLOROUS ACID; MYELOPEROXIDASE; OXIDIZING AGENT; PROTEINASE; OXYGEN;

EID: 84903842129     PISSN: 09031936     EISSN: 13993003     Source Type: Journal    
DOI: 10.1183/09031936.00038114     Document Type: Editorial
Times cited : (35)

References (31)
  • 1
    • 84858294319 scopus 로고    scopus 로고
    • Oxidative stress and antioxidant therapy in cystic fibrosis
    • Galli F, Battistoni A, Gambari R, et al. Oxidative stress and antioxidant therapy in cystic fibrosis. Biochim Biophys Acta 2012; 1822: 690-713.
    • (2012) Biochim Biophys Acta , vol.1822 , pp. 690-713
    • Galli, F.1    Battistoni, A.2    Gambari, R.3
  • 2
    • 33751580475 scopus 로고    scopus 로고
    • Antioxidants in cystic fibrosis. Conclusions from the CF antioxidant workshop, Bethesda, Maryland
    • November 11-12, 2003
    • Cantin AM, White TB, Cross CE, et al. Antioxidants in cystic fibrosis. Conclusions from the CF antioxidant workshop, Bethesda, Maryland, November 11-12, 2003. Free Radic Biol Med 2007; 42: 15-31.
    • (2007) Free Radic Biol Med , vol.42 , pp. 15-31
    • Cantin, A.M.1    White, T.B.2    Cross, C.E.3
  • 3
    • 84880079298 scopus 로고    scopus 로고
    • Oxidative stress in COPD
    • Kirkham PA, Barnes PJ. Oxidative stress in COPD. Chest 2013; 144: 266-273.
    • (2013) Chest , vol.144 , pp. 266-273
    • Kirkham, P.A.1    Barnes, P.J.2
  • 4
    • 33750620057 scopus 로고    scopus 로고
    • Oxidative stress and redox regulation of lung inflammation in COPD
    • Rahman I, Adcock IM. Oxidative stress and redox regulation of lung inflammation in COPD. Eur Respir J 2006; 28: 219-242.
    • (2006) Eur Respir J , vol.28 , pp. 219-242
    • Rahman, I.1    Adcock, I.M.2
  • 5
    • 84866182329 scopus 로고    scopus 로고
    • Innate immunity in cystic fibrosis lung disease
    • Hartl D, Gaggar A, Bruscia E, et al. Innate immunity in cystic fibrosis lung disease. J Cyst Fibros 2012; 11: 363-382.
    • (2012) J Cyst Fibros , vol.11 , pp. 363-382
    • Hartl, D.1    Gaggar, A.2    Bruscia, E.3
  • 6
    • 0033806242 scopus 로고    scopus 로고
    • Oxidative stress and regulation of glutathione in lung inflammation
    • Rahman I, MacNee W. Oxidative stress and regulation of glutathione in lung inflammation. Eur Respir J 2000; 16: 534-554.
    • (2000) Eur Respir J , vol.16 , pp. 534-554
    • Rahman, I.1    Macnee, W.2
  • 7
    • 0027742895 scopus 로고
    • Systemic deficiency of glutathione in cystic fibrosis
    • Roum JH, Buhl R, McElvaney NG, et al. Systemic deficiency of glutathione in cystic fibrosis. J Appl Physiol 1993; 75: 2419-2424.
    • (1993) J Appl Physiol , vol.75 , pp. 2419-2424
    • Roum, J.H.1    Buhl, R.2    McElvaney, N.G.3
  • 8
    • 80052715046 scopus 로고    scopus 로고
    • Current concepts of hyperinflammation in chronic granulomatous disease
    • Rieber N, Hector A, Kuijpers T, et al. Current concepts of hyperinflammation in chronic granulomatous disease. Clin Dev Immunol 2012; 2012: 252460.
    • (2012) Clin Dev Immunol , vol.2012 , pp. 252460
    • Rieber, N.1    Hector, A.2    Kuijpers, T.3
  • 9
    • 0035876878 scopus 로고    scopus 로고
    • Rethinking cystic fibrosis pathology: The critical role of abnormal reduced glutathione (GSH) transport caused by CFTR mutation
    • Hudson VM. Rethinking cystic fibrosis pathology: the critical role of abnormal reduced glutathione (GSH) transport caused by CFTR mutation. Free Radic Biol Med 2001; 30: 1440-1461.
    • (2001) Free Radic Biol Med , vol.30 , pp. 1440-1461
    • Hudson, V.M.1
  • 10
    • 0344258132 scopus 로고    scopus 로고
    • Abnormal glutathione transport in cystic fibrosis airway epithelia
    • Gao L, Kim KJ, Yankaskas JR, et al. Abnormal glutathione transport in cystic fibrosis airway epithelia. Am J Physiol 1999; 277: L113-L118.
    • (1999) Am J Physiol , vol.277
    • Gao, L.1    Kim, K.J.2    Yankaskas, J.R.3
  • 11
    • 1842431869 scopus 로고    scopus 로고
    • Role for cystic fibrosis transmembrane conductance regulator protein in a glutathione response to bronchopulmonary Pseudomonas infection
    • Day BJ, van Heeckeren AM, Min E, et al. Role for cystic fibrosis transmembrane conductance regulator protein in a glutathione response to bronchopulmonary Pseudomonas infection. Infect Immun 2004; 72: 2045-2051.
    • (2004) Infect Immun , vol.72 , pp. 2045-2051
    • Day, B.J.1    Van Heeckeren, A.M.2    Min, E.3
  • 12
    • 0030708939 scopus 로고    scopus 로고
    • Oxidation of neutrophil glutathione and protein thiols by myeloperoxidase-derived hypochlorous acid
    • Carr AC, Winterbourn CC. Oxidation of neutrophil glutathione and protein thiols by myeloperoxidase-derived hypochlorous acid. Biochem J 1997; 327: 275-281.
    • (1997) Biochem J , vol.327 , pp. 275-281
    • Carr, A.C.1    Winterbourn, C.C.2
  • 13
    • 84903830061 scopus 로고    scopus 로고
    • Oxidation contributes to low glutathione in the airways of children with cystic fibrosis
    • Kettle AJ, Turner, R, Gangell CL, et al. Oxidation contributes to low glutathione in the airways of children with cystic fibrosis. Eur Respir J 2014; 44: 122-129.
    • (2014) Eur Respir J , vol.44 , pp. 122-129
    • Kettle, A.J.1    Turner, R.2    Gangell, C.L.3
  • 14
    • 71749084479 scopus 로고    scopus 로고
    • Levels of nitric oxide oxidation products are increased in the epithelial lining fluid of children with persistent asthma
    • Fitzpatrick AM, Brown LA, Holguin F, et al. Levels of nitric oxide oxidation products are increased in the epithelial lining fluid of children with persistent asthma. J Allergy Clin Immunol 2009; 124: 990-996.
    • (2009) J Allergy Clin Immunol , vol.124 , pp. 990-996
    • Fitzpatrick, A.M.1    Brown, L.A.2    Holguin, F.3
  • 15
    • 0030802906 scopus 로고    scopus 로고
    • Pulmonary oxidative stress response in young children with cystic fibrosis
    • Hull J, Vervaart P, Grimwood K, et al. Pulmonary oxidative stress response in young children with cystic fibrosis. Thorax 1997; 52: 557-560.
    • (1997) Thorax , vol.52 , pp. 557-560
    • Hull, J.1    Vervaart, P.2    Grimwood, K.3
  • 16
    • 7444252099 scopus 로고    scopus 로고
    • Potential for antioxidant therapy of cystic fibrosis
    • Cantin AM. Potential for antioxidant therapy of cystic fibrosis. Curr Opin Pulm Med 2004; 10: 531-536.
    • (2004) Curr Opin Pulm Med , vol.10 , pp. 531-536
    • Cantin, A.M.1
  • 17
    • 33645229803 scopus 로고    scopus 로고
    • High-dose oral N-acetylcysteine, a glutathione prodrug, modulates inflammation in cystic fibrosis
    • Tirouvanziam R, Conrad CK, Bottiglieri T, et al. High-dose oral N-acetylcysteine, a glutathione prodrug, modulates inflammation in cystic fibrosis. Proc Nat Acad Sci USA 2006; 103: 4628-4633.
    • (2006) Proc Nat Acad Sci USA , vol.103 , pp. 4628-4633
    • Tirouvanziam, R.1    Conrad, C.K.2    Bottiglieri, T.3
  • 18
    • 12144289811 scopus 로고    scopus 로고
    • Improvement of alveolar glutathione and lung function but not oxidative state in cystic fibrosis
    • Griese M, Ramakers J, Krasselt A, et al. Improvement of alveolar glutathione and lung function but not oxidative state in cystic fibrosis. Am J Respir Crit Care Med 2004; 169: 822-828.
    • (2004) Am J Respir Crit Care Med , vol.169 , pp. 822-828
    • Griese, M.1    Ramakers, J.2    Krasselt, A.3
  • 19
    • 84880170145 scopus 로고    scopus 로고
    • Inhalation treatment with glutathione in patients with cystic fibrosis. A randomized clinical trial
    • Griese M, Kappler M, Eismann C, et al. Inhalation treatment with glutathione in patients with cystic fibrosis. A randomized clinical trial. Am J Respir Crit Care Med 2013; 188: 83-89.
    • (2013) Am J Respir Crit Care Med , vol.188 , pp. 83-89
    • Griese, M.1    Kappler, M.2    Eismann, C.3
  • 20
    • 67650764457 scopus 로고    scopus 로고
    • Nebulized and oral thiol derivatives for pulmonary disease in cystic fibrosis
    • Nash EF, Stephenson A, Ratjen F, et al. Nebulized and oral thiol derivatives for pulmonary disease in cystic fibrosis. Cochrane Databases Syst Rev 2009; 1: CD007168.
    • (2009) Cochrane Databases Syst Rev , vol.1
    • Nash, E.F.1    Stephenson, A.2    Ratjen, F.3
  • 21
    • 0032779834 scopus 로고    scopus 로고
    • Glutathione aerosol suppresses lung epithelial surface inflammatory cellderived oxidants in cystic fibrosis
    • Roum JH, Borok Z, McElvaney NG, et al. Glutathione aerosol suppresses lung epithelial surface inflammatory cellderived oxidants in cystic fibrosis. J Appl Physiol 1999; 87: 438-443.
    • (1999) J Appl Physiol , vol.87 , pp. 438-443
    • Roum, J.H.1    Borok, Z.2    McElvaney, N.G.3
  • 22
    • 22544453909 scopus 로고    scopus 로고
    • Inhaled glutathione decreases PGE2 and increases lymphocytes in cystic fibrosis lungs
    • Hartl D, Starosta V, Maier K, et al. Inhaled glutathione decreases PGE2 and increases lymphocytes in cystic fibrosis lungs. Free Radic Biol Med 2005; 39: 463-472.
    • (2005) Free Radic Biol Med , vol.39 , pp. 463-472
    • Hartl, D.1    Starosta, V.2    Maier, K.3
  • 23
    • 33846907545 scopus 로고    scopus 로고
    • A1-Antitrypsin inhalation reduces airway inflammation in cystic fibrosis patients
    • Griese M, Latzin P, Kappler M, et al. a1-Antitrypsin inhalation reduces airway inflammation in cystic fibrosis patients. Eur Respir J 2007; 29: 240-250.
    • (2007) Eur Respir J , vol.29 , pp. 240-250
    • Griese, M.1    Latzin, P.2    Kappler, M.3
  • 24
    • 58149394958 scopus 로고    scopus 로고
    • Inhibition of airway proteases in cystic fibrosis lung disease
    • Griese M, Kappler M, Gaggar A, et al. Inhibition of airway proteases in cystic fibrosis lung disease. Eur Respir J 2008; 32: 783-795.
    • (2008) Eur Respir J , vol.32 , pp. 783-795
    • Griese, M.1    Kappler, M.2    Gaggar, A.3
  • 25
    • 0025966879 scopus 로고
    • Aerosol a1-antitrypsin treatment for cystic fibrosis
    • McElvaney NG, Hubbard RC, Birrer P, et al. Aerosol a1-antitrypsin treatment for cystic fibrosis. Lancet 1991; 337: 392-394.
    • (1991) Lancet , vol.337 , pp. 392-394
    • McElvaney, N.G.1    Hubbard, R.C.2    Birrer, P.3
  • 26
    • 84878000440 scopus 로고    scopus 로고
    • Risk factors for bronchiectasis in children with cystic fibrosis
    • Sly PD, Gangell CL, Chen L, et al. Risk factors for bronchiectasis in children with cystic fibrosis. N Engl J Med 2013; 368: 1963-1970.
    • (2013) N Engl J Med , vol.368 , pp. 1963-1970
    • Sly, P.D.1    Gangell, C.L.2    Chen, L.3
  • 27
    • 84877953429 scopus 로고    scopus 로고
    • Identifying the origins of cystic fibrosis lung disease
    • Davis SD, Ferkol T. Identifying the origins of cystic fibrosis lung disease. N Engl J Med 2013; 368: 2026-2028.
    • (2013) N Engl J Med , vol.368 , pp. 2026-2028
    • Davis, S.D.1    Ferkol, T.2
  • 28
    • 84867023209 scopus 로고    scopus 로고
    • Evaluation and use of childhood lung function tests in cystic fibrosis
    • Stocks J, Thia LP, Sonnappa S. Evaluation and use of childhood lung function tests in cystic fibrosis. Curr Opin Pulm Med 2012; 18: 602-608.
    • (2012) Curr Opin Pulm Med , vol.18 , pp. 602-608
    • Stocks, J.1    Thia, L.P.2    Sonnappa, S.3
  • 29
    • 84873393070 scopus 로고    scopus 로고
    • A new double-tracer gas single-breath washout to assess early cystic fibrosis lung disease
    • Singer F, Stern G, Thamrin C, et al. A new double-tracer gas single-breath washout to assess early cystic fibrosis lung disease. Eur Respir J 2013; 41: 339-345.
    • (2013) Eur Respir J , vol.41 , pp. 339-345
    • Singer, F.1    Stern, G.2    Thamrin, C.3
  • 30
    • 79952504576 scopus 로고    scopus 로고
    • Lung clearance index at 4 years predicts subsequent lung function in children with cystic fibrosis
    • Aurora P, Stanojevic S, Wade A, et al. Lung clearance index at 4 years predicts subsequent lung function in children with cystic fibrosis. Am J Respir Crit Care Med 2011; 183: 752-758.
    • (2011) Am J Respir Crit Care Med , vol.183 , pp. 752-758
    • Aurora, P.1    Stanojevic, S.2    Wade, A.3


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