Pneumonia-Induced Sepsis and Gut Injury: Effects of a Poly-(ADP-Ribose) Polymerase Inhibitor
Pseudomonas aeruginosa is commonly associated with nosocomial pneumonia. Ileal mucosal injury may be induced by severe lung infection. During septic shock, peroxynitrite-mediated DNA strand-breaks activate the enzyme poly-(ADP)-ribose polymerase (PARP) resulting in cellular energetic suppression and...
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Published in: | The Journal of surgical research Vol. 129; no. 2; pp. 292 - 297 |
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Abstract | Pseudomonas aeruginosa is commonly associated with nosocomial pneumonia. Ileal mucosal injury may be induced by severe lung infection. During septic shock, peroxynitrite-mediated DNA strand-breaks activate the enzyme poly-(ADP)-ribose polymerase (PARP) resulting in cellular energetic suppression and cell dysfunction. The aim of this study was to determine whether gut injury could be demonstrated in sepsis induced by
P. aeruginosa and the effects of a PARP inhibitor (PJ34) on the associated gut injury.
After baseline measurements, 20 rabbits were randomized into three groups: Sham (
n = 5): transtracheally inoculated (TI) with 2 ml of phosphate buffer solution (PBS);
P. aeruginosa + saline (
n = 8), TI with 4 × 10
12 CFU/ml of
P. aeruginosa in 2 ml/kg of PBS + i.v. saline; and
P. aeruginosa + PJ34 (
n = 7), TI with 4 × 10
12 CFU/ml of
P. aeruginosa and i.v. treatment with PJ34.
P. aeruginosa caused a hyperdynamic response with increased blood flow also in the superior mesenteric artery. No significant differences were found in luminal gut lactate concentrations or PCO
2-gap between groups. Histological specimens showed moderate or diffuse alveolar infiltrate in the
P. aeruginosa + saline group (6/8) and in the
P. aeruginosa + PJ34 group (6/7). Gut wet-to-dry weight ratio was significantly higher in the
P. aeruginosa + saline group than in Shams (7.5 ± 0.8
versus 6.4 ± 0.7,
P < 0.05) and significantly lower in the
P. aeruginosa + PJ34 group (6.1 + 0.5,
P < 0.05
versus the other groups). Blood cultures were positive in 1/5 (Sham), 8/8 (
P. aeruginosa + saline group) and 4/7 (
P. aeruginosa + PJ34 group) (RR 0.57 CI 95% 0.30–1.08).
Pharmacological inhibition of PARP reduces gut inflammation and may limit bacterial translocation. |
---|---|
AbstractList | BACKGROUNDPseudomonas aeruginosa is commonly associated with nosocomial pneumonia. Ileal mucosal injury may be induced by severe lung infection. During septic shock, peroxynitrite-mediated DNA strand-breaks activate the enzyme poly-(ADP)-ribose polymerase (PARP) resulting in cellular energetic suppression and cell dysfunction. The aim of this study was to determine whether gut injury could be demonstrated in sepsis induced by P. aeruginosa and the effects of a PARP inhibitor (PJ34) on the associated gut injury.MATERIALS AND METHODSAfter baseline measurements, 20 rabbits were randomized into three groups: Sham (n = 5): transtracheally inoculated (TI) with 2 ml of phosphate buffer solution (PBS); P. aeruginosa + saline (n = 8), TI with 4 x 10(12) CFU/ml of P. aeruginosa in 2 ml/kg of PBS + i.v. saline; and P. aeruginosa + PJ34 (n = 7), TI with 4 x 10(12) CFU/ml of P. aeruginosa and i.v. treatment with PJ34.RESULTSP. aeruginosa caused a hyperdynamic response with increased blood flow also in the superior mesenteric artery. No significant differences were found in luminal gut lactate concentrations or PCO(2)-gap between groups. Histological specimens showed moderate or diffuse alveolar infiltrate in the P. aeruginosa + saline group (6/8) and in the P. aeruginosa + PJ34 group (6/7). Gut wet-to-dry weight ratio was significantly higher in the P. aeruginosa + saline group than in Shams (7.5 +/- 0.8 versus 6.4 +/- 0.7, P < 0.05) and significantly lower in the P. aeruginosa + PJ34 group (6.1 + 0.5, P < 0.05 versus the other groups). Blood cultures were positive in 1/5 (Sham), 8/8 (P. aeruginosa + saline group) and 4/7 (P. aeruginosa + PJ34 group) (RR 0.57 CI 95% 0.30-1.08).CONCLUSIONSPharmacological inhibition of PARP reduces gut inflammation and may limit bacterial translocation. Pseudomonas aeruginosa is commonly associated with nosocomial pneumonia. Ileal mucosal injury may be induced by severe lung infection. During septic shock, peroxynitrite-mediated DNA strand-breaks activate the enzyme poly-(ADP)-ribose polymerase (PARP) resulting in cellular energetic suppression and cell dysfunction. The aim of this study was to determine whether gut injury could be demonstrated in sepsis induced by P. aeruginosa and the effects of a PARP inhibitor (PJ34) on the associated gut injury. After baseline measurements, 20 rabbits were randomized into three groups: Sham (n = 5): transtracheally inoculated (TI) with 2 ml of phosphate buffer solution (PBS); P. aeruginosa + saline (n = 8), TI with 4 x 10(12) CFU/ml of P. aeruginosa in 2 ml/kg of PBS + i.v. saline; and P. aeruginosa + PJ34 (n = 7), TI with 4 x 10(12) CFU/ml of P. aeruginosa and i.v. treatment with PJ34. P. aeruginosa caused a hyperdynamic response with increased blood flow also in the superior mesenteric artery. No significant differences were found in luminal gut lactate concentrations or PCO(2)-gap between groups. Histological specimens showed moderate or diffuse alveolar infiltrate in the P. aeruginosa + saline group (6/8) and in the P. aeruginosa + PJ34 group (6/7). Gut wet-to-dry weight ratio was significantly higher in the P. aeruginosa + saline group than in Shams (7.5 +/- 0.8 versus 6.4 +/- 0.7, P < 0.05) and significantly lower in the P. aeruginosa + PJ34 group (6.1 + 0.5, P < 0.05 versus the other groups). Blood cultures were positive in 1/5 (Sham), 8/8 (P. aeruginosa + saline group) and 4/7 (P. aeruginosa + PJ34 group) (RR 0.57 CI 95% 0.30-1.08). Pharmacological inhibition of PARP reduces gut inflammation and may limit bacterial translocation. Pseudomonas aeruginosa is commonly associated with nosocomial pneumonia. Ileal mucosal injury may be induced by severe lung infection. During septic shock, peroxynitrite-mediated DNA strand-breaks activate the enzyme poly-(ADP)-ribose polymerase (PARP) resulting in cellular energetic suppression and cell dysfunction. The aim of this study was to determine whether gut injury could be demonstrated in sepsis induced by P. aeruginosa and the effects of a PARP inhibitor (PJ34) on the associated gut injury. After baseline measurements, 20 rabbits were randomized into three groups: Sham ( n = 5): transtracheally inoculated (TI) with 2 ml of phosphate buffer solution (PBS); P. aeruginosa + saline ( n = 8), TI with 4 × 10 12 CFU/ml of P. aeruginosa in 2 ml/kg of PBS + i.v. saline; and P. aeruginosa + PJ34 ( n = 7), TI with 4 × 10 12 CFU/ml of P. aeruginosa and i.v. treatment with PJ34. P. aeruginosa caused a hyperdynamic response with increased blood flow also in the superior mesenteric artery. No significant differences were found in luminal gut lactate concentrations or PCO 2-gap between groups. Histological specimens showed moderate or diffuse alveolar infiltrate in the P. aeruginosa + saline group (6/8) and in the P. aeruginosa + PJ34 group (6/7). Gut wet-to-dry weight ratio was significantly higher in the P. aeruginosa + saline group than in Shams (7.5 ± 0.8 versus 6.4 ± 0.7, P < 0.05) and significantly lower in the P. aeruginosa + PJ34 group (6.1 + 0.5, P < 0.05 versus the other groups). Blood cultures were positive in 1/5 (Sham), 8/8 ( P. aeruginosa + saline group) and 4/7 ( P. aeruginosa + PJ34 group) (RR 0.57 CI 95% 0.30–1.08). Pharmacological inhibition of PARP reduces gut inflammation and may limit bacterial translocation. |
Author | Orrico, Susana R. Perez Togni, Paulo Preiser, Jean-Charles de Almeida Burdmann, Emanuel Lobo, Suzana M. Chibeni, Gisela S.A. Queiroz, Márcio M. Cunrath, Geni S. Vincent, Jean-Louis Contrin, Ligia M. Cury, Patricia M. Szabó, Czaba de Oliveira Machado, Antonia M. De Backer, Daniel |
Author_xml | – sequence: 1 givenname: Suzana M. surname: Lobo fullname: Lobo, Suzana M. organization: Intensive Care Unit, Hospital de Base - Faculdade de Medicina, Sao Jose do Rio Preto, Brazil – sequence: 2 givenname: Susana R. Perez surname: Orrico fullname: Orrico, Susana R. Perez organization: Intensive Care Unit, Hospital de Base - Faculdade de Medicina, Sao Jose do Rio Preto, Brazil – sequence: 3 givenname: Márcio M. surname: Queiroz fullname: Queiroz, Márcio M. organization: Intensive Care Unit, Hospital de Base - Faculdade de Medicina, Sao Jose do Rio Preto, Brazil – sequence: 4 givenname: Geni S. surname: Cunrath fullname: Cunrath, Geni S. organization: Intensive Care Unit, Hospital de Base - Faculdade de Medicina, Sao Jose do Rio Preto, Brazil – sequence: 5 givenname: Gisela S.A. surname: Chibeni fullname: Chibeni, Gisela S.A. organization: Intensive Care Unit, Hospital de Base - Faculdade de Medicina, Sao Jose do Rio Preto, Brazil – sequence: 6 givenname: Ligia M. surname: Contrin fullname: Contrin, Ligia M. organization: Intensive Care Unit, Hospital de Base - Faculdade de Medicina, Sao Jose do Rio Preto, Brazil – sequence: 7 givenname: Patricia M. surname: Cury fullname: Cury, Patricia M. organization: Intensive Care Unit, Hospital de Base - Faculdade de Medicina, Sao Jose do Rio Preto, Brazil – sequence: 8 givenname: Emanuel surname: de Almeida Burdmann fullname: de Almeida Burdmann, Emanuel organization: Intensive Care Unit, Hospital de Base - Faculdade de Medicina, Sao Jose do Rio Preto, Brazil – sequence: 9 givenname: Antonia M. surname: de Oliveira Machado fullname: de Oliveira Machado, Antonia M. organization: Intensive Care Unit, Hospital de Base - Faculdade de Medicina, Sao Jose do Rio Preto, Brazil – sequence: 10 givenname: Paulo surname: Togni fullname: Togni, Paulo organization: Radiology department, FAMECA, Catanduva, Brazil – sequence: 11 givenname: Daniel surname: De Backer fullname: De Backer, Daniel organization: Department of Intensive Care, Erasme Hospital-Free University of Brussels, Belgium – sequence: 12 givenname: Jean-Charles surname: Preiser fullname: Preiser, Jean-Charles organization: Department of Intensive Care, Erasme Hospital-Free University of Brussels, Belgium – sequence: 13 givenname: Czaba surname: Szabó fullname: Szabó, Czaba organization: Inotek Pharmaceuticals Corporation, Beverly, Massachusetts – sequence: 14 givenname: Jean-Louis surname: Vincent fullname: Vincent, Jean-Louis email: jlvincen@ulb.ac.be organization: Department of Intensive Care, Erasme Hospital-Free University of Brussels, Belgium |
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Keywords | Pseudomonas aeruginosa bacterial translocation gut inflammation Chromosomal aberration Pseudomonadales Pneumonia ADP Sepsis syndrome Ribose Surgery Bacteria Pseudomonadaceae Chromosome translocation Lung disease Respiratory disease Gut Inflammation Bacteremia Infection Medicine Treatment Bacteriosis Cytogenetics Abnormal chromosome Inhibitor Lesion |
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Snippet | Pseudomonas aeruginosa is commonly associated with nosocomial pneumonia. Ileal mucosal injury may be induced by severe lung infection. During septic shock,... BACKGROUNDPseudomonas aeruginosa is commonly associated with nosocomial pneumonia. Ileal mucosal injury may be induced by severe lung infection. During septic... |
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SubjectTerms | Animals Aorta Bacterial diseases Bacterial sepsis bacterial translocation Biological and medical sciences Blood Pressure Enteritis - drug therapy Enteritis - microbiology Enzyme Inhibitors - pharmacology General aspects gut inflammation Human bacterial diseases Infectious diseases Intestines - blood supply Intestines - microbiology Intestines - pathology Medical sciences Mesenteric Artery, Superior Phenanthrenes - pharmacology Pneumonia, Bacterial - complications Pneumonia, Bacterial - drug therapy Pneumonia, Bacterial - microbiology Poly(ADP-ribose) Polymerase Inhibitors Pseudomonas aeruginosa Pseudomonas aeruginosa - isolation & purification Pseudomonas Infections - drug therapy Pseudomonas Infections - etiology Rabbits Regional Blood Flow Sepsis - drug therapy Sepsis - microbiology Specific Pathogen-Free Organisms Trachea |
Title | Pneumonia-Induced Sepsis and Gut Injury: Effects of a Poly-(ADP-Ribose) Polymerase Inhibitor |
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