Evidence mapPaperPMID 28192604Full record

ArticleBritish journal of pharmacology2017

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

Annika Åstrand, Cecilia Wingren, Audra Benjamin, John S Tregoning, James P Garnett, Helen Groves, Simren Gill, Maria Orogo-Wenn, Anders J Lundqvist, Dafydd Walters and 4 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 2 pooled it
1.8field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 2 syntheses or guidelines pooled it, 53 citations in OpenAlex.

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  10. The presence of cystic fibrosis-related diabetes modifies the sputum microbiome in cystic fibrosis disease.American journal of physiology. Lung cellular and molecular physiology · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 3 institutions in 2 countries.

Annika ÅstrandRespiratory, Inflammation and Autoimmunity Innovative Medicines Research Unit, AstraZeneca Gothenburg, Mölndal, Sweden.
Cecilia WingrenRespiratory, Inflammation and Autoimmunity Innovative Medicines Research Unit, AstraZeneca Gothenburg, Mölndal, Sweden.
Audra BenjaminInstitute for Infection and Immunity, St George's, University of London, London, UK.
John S TregoningMucosal Infection & Immunity Group, Section of Virology, Imperial College London, St Mary's Campus, London, UK.
James P GarnettInstitute for Infection and Immunity, St George's, University of London, London, UK.
Helen GrovesMucosal Infection & Immunity Group, Section of Virology, Imperial College London, St Mary's Campus, London, UK.
Simren GillMucosal Infection & Immunity Group, Section of Virology, Imperial College London, St Mary's Campus, London, UK.
Maria Orogo-WennInstitute for Infection and Immunity, St George's, University of London, London, UK.
Anders J LundqvistRespiratory, Inflammation and Autoimmunity Innovative Medicines Research Unit, AstraZeneca Gothenburg, Mölndal, Sweden.
Dafydd WaltersInstitute for Infection and Immunity, St George's, University of London, London, UK.
David M SmithCardiovascular & Metabolic Diseases Innovative Medicines Research Unit, AstraZeneca Gothenburg, Mölndal, Sweden.
John D TaylorRespiratory, Inflammation and Autoimmunity Innovative Medicines Research Unit, AstraZeneca Gothenburg, Mölndal, Sweden.
Emma H BakerInstitute for Infection and Immunity, St George's, University of London, London, UK.
Deborah L BainesInstitute for Infection and Immunity, St George's, University of London, London, UK.
St George's, University of London · GBAstraZeneca (Sweden) · SEImperial College London · GB

Funding

Medical Research Council MR/K012770/1MRF_ MRF-091-0001-RG-GARNE
6 · The paper itself

Abstract

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 APPROACH: The 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 IMPLICATIONS: Pharmacological 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.

Indexed as

AnimalsBenzhydryl CompoundsBlood GlucoseBronchoalveolar Lavage FluidDiabetes Mellitus, ExperimentalGlucosidesMaleMiceMice, Inbred C57BLMice, TransgenicPseudomonas aeruginosaPseudomonas InfectionsRatsRats, WistarSodium-Glucose Transport ProteinsBenzhydryl CompoundsBlood GlucosedapagliflozinGlucosidesSodium-Glucose Transport Proteins

Identifiers

PMID28192604
PMCPMC5386993
OpenAlexW2587900704

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.