Dapagliflozin-lowered blood glucose reduces respiratory Pseudomonas aeruginosa infection in diabetic mice

被引:30
作者
Astrand, Annika [1 ]
Wingren, Cecilia [1 ]
Benjamin, Audra [2 ]
Tregoning, John S. [3 ]
Garnett, James P. [2 ]
Groves, Helen [3 ]
Gill, Simren [3 ]
Orogo-Wenn, Maria [2 ]
Lundqvist, Anders J. [1 ]
Walters, Dafydd [2 ]
Smith, David M. [4 ]
Taylor, John D. [1 ]
Baker, Emma H. [2 ]
Baines, Deborah L. [2 ]
机构
[1] AstraZeneca Gothenburg, Resp Inflammat & Autoimmun Innovat Med Res Unit, Molndal, Sweden
[2] Univ London, Inst Infect & Immun, London SW17 0RE, England
[3] Imperial Coll London, Sect Virol, Mucosal Infect & Immun Grp, St Marys Campus, London, England
[4] AstraZeneca Gothenburg, Cardiovasc & Metab Dis Innovat Med Res Unit, Molndal, Sweden
基金
英国医学研究理事会;
关键词
CYSTIC-FIBROSIS; METABOLIC SYNDROME; SGLT2; INHIBITOR; CONCISE GUIDE; LUNG-FUNCTION; HYPERGLYCEMIA; RISK; EXACERBATION; PHARMACOLOGY; MELLITUS;
D O I
10.1111/bph.13741
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background and PurposeHyperglycaemia increases glucose concentrations in airway surface liquid and increases the risk of pulmonary Pseudomonas aeruginosa infection. We determined whether reduction of blood and airway glucose concentrations by the anti-diabetic drug dapagliflozin could reduce P.aeruginosa growth/survival in the lungs of diabetic mice. Experimental ApproachThe effect of dapagliflozin on blood and airway glucose concentration, the inflammatory response and infection were investigated in C57BL/6J (wild type, WT) or leptin receptor-deficient (db/db) mice, treated orally with dapagliflozin prior to intranasal dosing with LPS or inoculation with P.aeruginosa. Pulmonary glucose transport and fluid absorption were investigated in Wistar rats using the perfused fluid-filled lung technique. Key ResultsFasting blood, airway glucose and lactate concentrations were elevated in the db/db mouse lung. LPS challenge increased inflammatory cells in bronchoalveolar lavage fluid from WT and db/db mice with and without dapagliflozin treatment. P.aeruginosa colony-forming units (CFU) were increased in db/db lungs. Pretreatment with dapagliflozin reduced blood and bronchoalveolar lavage glucose concentrations and P.aeruginosa CFU in db/db mice towards those seen in WT. Dapagliflozin had no adverse effects on the inflammatory response in the mouse or pulmonary glucose transport or fluid absorption in the rat lung. Conclusion and ImplicationsPharmacological lowering of blood glucose with dapagliflozin effectively reduced P.aeruginosa infection in the lungs of diabetic mice and had no adverse pulmonary effects in the rat. Dapagliflozin has potential to reduce the use, or augment the effect, of antimicrobials in the prevention or treatment of pulmonary infection.
引用
收藏
页码:836 / 847
页数:12
相关论文
共 45 条
[1]   THE CONCISE GUIDE TO PHARMACOLOGY 2015/16: Catalytic receptors [J].
Alexander, Stephen P. H. ;
Fabbro, Doriano ;
Kelly, Eamonn ;
Marrion, Neil ;
Peters, John A. ;
Benson, Helen E. ;
Faccenda, Elena ;
Pawson, Adam J. ;
Sharman, Joanna L. ;
Southan, Christopher ;
Davies, Jamie A. ;
Aldrich, R. ;
Attali, B. ;
Back, M. ;
Barnes, N. M. ;
Bathgate, R. ;
Beart, P. M. ;
Becirovic, E. ;
Biel, M. ;
Birdsall, N. J. ;
Boison, D. ;
Brauner-Osborne, H. ;
Broeer, S. ;
Bryant, C. ;
Burnstock, G. ;
Burris, T. ;
Cain, D. ;
Calo, G. ;
Chan, S. L. ;
Chandy, K. G. ;
Chiang, N. ;
Christakos, S. ;
Christopoulos, A. ;
Chun, J. J. ;
Chung, J. -J. ;
Clapham, D. E. ;
Connor, M. A. ;
Coons, L. ;
Cox, H. M. ;
Dautzenberg, F. M. ;
Dent, G. ;
Douglas, S. D. ;
Dubocovich, M. L. ;
Edwards, D. P. ;
Farndale, R. ;
Fong, T. M. ;
Forrest, D. ;
Fowler, C. J. ;
Fuller, P. ;
Gainetdinov, R. R. .
BRITISH JOURNAL OF PHARMACOLOGY, 2015, 172 (24) :5979-6023
[2]   THE CONCISE GUIDE TO PHARMACOLOGY 2015/16: Transporters [J].
Alexander, Stephen P. H. ;
Kelly, Eamonn ;
Marrion, Neil ;
Peters, John A. ;
Benson, Helen E. ;
Faccenda, Elena ;
Pawson, Adam J. ;
Sharman, Joanna L. ;
Southan, Christopher ;
Davies, Jamie A. ;
Aldrich, R. ;
Attali, B. ;
Back, M. ;
Barnes, N. M. ;
Bathgate, R. ;
Beart, P. M. ;
Becirovic, E. ;
Biel, M. ;
Birdsall, N. J. ;
Boison, D. ;
Brauner-Osborne, H. ;
Broeer, S. ;
Bryant, C. ;
Burnstock, G. ;
Burris, T. ;
Cain, D. ;
Calo, G. ;
Chan, S. L. ;
Chandy, K. G. ;
Chiang, N. ;
Christakos, S. ;
Christopoulos, A. ;
Chun, J. J. ;
Chung, J. -J. ;
Clapham, D. E. ;
Connor, M. A. ;
Coons, L. ;
Cox, H. M. ;
Dautzenberg, F. M. ;
Dent, G. ;
Douglas, S. D. ;
Dubocovich, M. L. ;
Edwards, D. P. ;
Farndale, R. ;
Fong, T. M. ;
Forrest, D. ;
Fowler, C. J. ;
Fuller, P. ;
Gainetdinov, R. R. ;
Gershengorn, M. A. .
BRITISH JOURNAL OF PHARMACOLOGY, 2015, 172 (24) :6110-6202
[3]   GLYCEMIC EFFECTS OF SGLT-2 INHIBITOR CANAGLIFLOZIN IN TYPE 1 DIABETES PATIENTS USING THE DEXCOM G4 PLATINUM CGM [J].
Argento, Nicholas B. ;
Nakamura, Katherine .
ENDOCRINE PRACTICE, 2016, 22 (03) :315-322
[4]   Hyperglycemia and cystic fibrosis alter respiratory fluid glucose concentrations estimated by breath condensate analysis [J].
Baker, Emma H. ;
Clark, Nicholas ;
Brennan, Amanda L. ;
Fisher, Donald A. ;
Gyi, Khin M. ;
Hodson, Margaret E. ;
Philips, Barbara J. ;
Baines, Deborah L. ;
Wood, David M. .
JOURNAL OF APPLIED PHYSIOLOGY, 2007, 102 (05) :1969-1975
[5]   Evidence for Na+-glucose cotransporter in type I alveolar epithelium [J].
Bodega, Francesca ;
Sironi, Chiara ;
Armilli, Marta ;
Porta, Cristina ;
Agostoni, Emilio .
HISTOCHEMISTRY AND CELL BIOLOGY, 2010, 134 (02) :129-136
[6]   Oral antimicrobial use in outpatient cystic fibrosis pulmonary exacerbation management: a single-center experience [J].
Briggs, Elissa Charlotte ;
Thuan Nguyen ;
Wall, Michael Abraham ;
MacDonald, Kelvin David .
CLINICAL RESPIRATORY JOURNAL, 2012, 6 (01) :56-64
[7]   Experimental design and analysis and their reporting: new guidance for publication in BJP [J].
Curtis, Michael J. ;
Bond, Richard A. ;
Spina, Domenico ;
Ahluwalia, Amrita ;
Alexander, Stephen P. A. ;
Giembycz, Mark A. ;
Gilchrist, Annette ;
Hoyer, Daniel ;
Insel, Paul A. ;
Izzo, Angelo A. ;
Lawrence, Andrew J. ;
MacEwan, David J. ;
Moon, Lawrence D. F. ;
Wonnacott, Sue ;
Weston, Arthur H. ;
McGrath, John C. .
BRITISH JOURNAL OF PHARMACOLOGY, 2015, 172 (14) :3461-3471
[8]  
Franzese A, 2008, J PEDIATR ENDOCR MET, V21, P109
[9]   Fructose transport-deficient Staphylococcus aureus reveals important role of epithelial glucose transporters in limiting sugar-driven bacterial growth in airway surface liquid [J].
Garnett, James P. ;
Braun, Daniela ;
McCarthy, Alex J. ;
Farrant, Matthew R. ;
Baker, Emma H. ;
Lindsay, Jodi A. ;
Baines, Deborah L. .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2014, 71 (23) :4665-4673
[10]   Elevated Paracellular Glucose Flux across Cystic Fibrosis Airway Epithelial Monolayers Is an Important Factor for Pseudomonas aeruginosa Growth [J].
Garnett, James P. ;
Gray, Michael A. ;
Tarran, Robert ;
Brodlie, Malcolm ;
Ward, Christopher ;
Baker, Emma H. ;
Baines, Deborah L. .
PLOS ONE, 2013, 8 (10)