Clinical Development of Sphingosine as Anti-Bacterial Drug: Inhalation of Sphingosine in Mini Pigs has no Adverse Side Effects.


Journal

Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology
ISSN: 1421-9778
Titre abrégé: Cell Physiol Biochem
Pays: Germany
ID NLM: 9113221

Informations de publication

Date de publication:
2019
Historique:
accepted: 12 12 2019
entrez: 20 12 2019
pubmed: 20 12 2019
medline: 25 12 2019
Statut: ppublish

Résumé

Pulmonary infections with Pseudomonas aeruginosa (P. aeruginosa) or Staphylococcus aureus (S. aureus) are of utmost clinical relevance in patients with cystic fibrosis, chronic obstructive pulmonary disease, after trauma and burn, upon ventilation or in immuno-compromised patients. Many P. aeruginosa and S. aureus strains are resistant to many known antibiotics and it is very difficult or often impossible to eradicate the pathogens in patient´s lungs. We have recently shown that the sphingoid base sphingosine very efficiently kills many pathogens, including for instance P. aeruginosa, S. aureus or Acinetobacter baumannii, in vitro. In vivo experiments of our group on cystic fibrosis mice indicated that inhalation of sphingosine prevents or eliminates existing acute or chronic pneumonia with P. aeruginosa or S. aureus in these mice. We also demonstrated that sphingosine is safe to use for inhalation up to high doses, at least in mice. To facilitate development of sphingosine to an anti-bactericidal drug that can be used in humans for inhalation, safety data on non-rodents, larger animals are absolutely required. Here, we inhaled mini pigs with increasing doses of sphingosine for 10 days and analyzed the uptake of sphingosine into epithelial cells of bronchi as well as into the trachea and lung and the systemic circulation. Moreover, we measured the generation of ceramide and sphingosine 1-phosphate that potentially mediate inflammation, the influx of leukocytes, epithelial cell death and disruption of the epithelial cell barrier. We demonstrate that inhalation of sphingosine results in increased levels of sphingosine in the luminal membrane of bronchi and the trachea, but not in systemic accumulation. Inhaled sphingosine had no side effects up to very high doses. In summary, we demonstrate that inhalation of sphingosine results in an increase of sphingosine concentrations in the luminal plasma membrane of tracheal and bronchial epithelial cells. The inhalation has no systemic or local side effects.

Sections du résumé

BACKGROUND/AIMS OBJECTIVE
Pulmonary infections with Pseudomonas aeruginosa (P. aeruginosa) or Staphylococcus aureus (S. aureus) are of utmost clinical relevance in patients with cystic fibrosis, chronic obstructive pulmonary disease, after trauma and burn, upon ventilation or in immuno-compromised patients. Many P. aeruginosa and S. aureus strains are resistant to many known antibiotics and it is very difficult or often impossible to eradicate the pathogens in patient´s lungs. We have recently shown that the sphingoid base sphingosine very efficiently kills many pathogens, including for instance P. aeruginosa, S. aureus or Acinetobacter baumannii, in vitro. In vivo experiments of our group on cystic fibrosis mice indicated that inhalation of sphingosine prevents or eliminates existing acute or chronic pneumonia with P. aeruginosa or S. aureus in these mice. We also demonstrated that sphingosine is safe to use for inhalation up to high doses, at least in mice. To facilitate development of sphingosine to an anti-bactericidal drug that can be used in humans for inhalation, safety data on non-rodents, larger animals are absolutely required.
METHODS METHODS
Here, we inhaled mini pigs with increasing doses of sphingosine for 10 days and analyzed the uptake of sphingosine into epithelial cells of bronchi as well as into the trachea and lung and the systemic circulation. Moreover, we measured the generation of ceramide and sphingosine 1-phosphate that potentially mediate inflammation, the influx of leukocytes, epithelial cell death and disruption of the epithelial cell barrier.
RESULTS RESULTS
We demonstrate that inhalation of sphingosine results in increased levels of sphingosine in the luminal membrane of bronchi and the trachea, but not in systemic accumulation. Inhaled sphingosine had no side effects up to very high doses.
CONCLUSION CONCLUSIONS
In summary, we demonstrate that inhalation of sphingosine results in an increase of sphingosine concentrations in the luminal plasma membrane of tracheal and bronchial epithelial cells. The inhalation has no systemic or local side effects.

Identifiants

pubmed: 31854953
doi: 10.33594/000000194
doi:

Substances chimiques

Anti-Bacterial Agents 0
Ceramides 0
Lysophospholipids 0
sphingosine 1-phosphate 26993-30-6
Sphingosine NGZ37HRE42

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1015-1028

Subventions

Organisme : Deutsche Forschungsgemeinschaft (DFG)
ID : GU 335/35-1
Pays : Germany

Informations de copyright

© Copyright by the Author(s). Published by Cell Physiol Biochem Press.

Déclaration de conflit d'intérêts

The authors have no conflicts of interest to declare.

Auteurs

Henning Carstens (H)

Thoracic Transplantation, Thoracic and Cardiovascular Surgery, University Clinic, University of Duisburg-Essen, Essen, Germany.

Fabian Schumacher (F)

Faculty of Mathematics and Natural Science, Institute of Nutritional Science, Department of Toxicology, University of Potsdam, Nuthetal, Potsdam, Germany.
Department of Molecular Biology, University Clinic, University of Duisburg-Essen, Essen, Germany.

Simone Keitsch (S)

Department of Molecular Biology, University Clinic, University of Duisburg-Essen, Essen, Germany.

Melanie Kramer (M)

Department of Molecular Biology, University Clinic, University of Duisburg-Essen, Essen, Germany.

Claudine Kühn (C)

Department of Molecular Biology, University Clinic, University of Duisburg-Essen, Essen, Germany.

Carolin Sehl (C)

Department of Molecular Biology, University Clinic, University of Duisburg-Essen, Essen, Germany.

Matthias Soddemann (M)

Department of Molecular Biology, University Clinic, University of Duisburg-Essen, Essen, Germany.

Barbara Wilker (B)

Department of Molecular Biology, University Clinic, University of Duisburg-Essen, Essen, Germany.

Daniel Herrmann (D)

Faculty of Mathematics and Natural Science, Institute of Nutritional Science, Department of Toxicology, University of Potsdam, Nuthetal, Potsdam, Germany.

Ashraf Swaidan (A)

Department of Molecular Biology, University Clinic, University of Duisburg-Essen, Essen, Germany.

Burkhard Kleuser (B)

Faculty of Mathematics and Natural Science, Institute of Nutritional Science, Department of Toxicology, University of Potsdam, Nuthetal, Potsdam, Germany.

Rabea Verhaegh (R)

Department of Molecular Biology, University Clinic, University of Duisburg-Essen, Essen, Germany.

Gero Hilken (G)

Central Animal Facility, University Clinic, University of Duisburg-Essen, Essen, Germany.

Michael J Edwards (MJ)

Department of Surgery, College of Medicine, University of Cincinnati, Cincinnati, Ohio, USA.

Marko Dubicanac (M)

Central Animal Facility, University Clinic, University of Duisburg-Essen, Essen, Germany.

Alexander Carpinteiro (A)

Department of Molecular Biology, University Clinic, University of Duisburg-Essen, Essen, Germany.
Department of Hematology, University Clinic, University of Duisburg-Essen, Essen, Germany.

Andreas Wissmann (A)

Central Animal Facility, University Clinic, University of Duisburg-Essen, Essen, Germany.

Katrin Anne Becker (KA)

Department of Molecular Biology, University Clinic, University of Duisburg-Essen, Essen, Germany.

Markus Kamler (M)

Thoracic Transplantation, Thoracic and Cardiovascular Surgery, University Clinic, University of Duisburg-Essen, Essen, Germany.

Erich Gulbins (E)

Department of Molecular Biology, University Clinic, University of Duisburg-Essen, Essen, Germany, erich.gulbins@uni-due.de.
Department of Surgery, College of Medicine, University of Cincinnati, Cincinnati, Ohio, USA.

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