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
Main Authors: Lobo, Suzana M., Orrico, Susana R. Perez, Queiroz, Márcio M., Cunrath, Geni S., Chibeni, Gisela S.A., Contrin, Ligia M., Cury, Patricia M., de Almeida Burdmann, Emanuel, de Oliveira Machado, Antonia M., Togni, Paulo, De Backer, Daniel, Preiser, Jean-Charles, Szabó, Czaba, Vincent, Jean-Louis
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Published: New York, NY Elsevier Inc 01-12-2005
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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
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  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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Issue 2
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
Language English
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PublicationTitle The Journal of surgical research
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SSID ssj0002973
Score 1.9182556
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
URI https://dx.doi.org/10.1016/j.jss.2005.05.018
https://www.ncbi.nlm.nih.gov/pubmed/16139303
https://search.proquest.com/docview/68910665
Volume 129
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