Inosine reduces systemic inflammation and improves survival in septic shock induced by cecal ligation and puncture

L. Liaudet, Jon Mabley, F.G. Soriano, P. Pacher, A. Marton, G. Hasko, C. Szabo

Research output: Contribution to journalArticle

Abstract

nosine is a naturally occurring purine formed from the breakdown of adenosine. Here we have evaluated the effects of inosine in a murine model of polymicrobial sepsis induced by cecal ligation and puncture (CLP). Mice subjected to CLP were treated with either inosine (100 mg/kg, intraperitoneally) or vehicle 1 h before and 6 h after CLP. After 12 h tumor necrosis factor alpha , interleukin 6 (IL-6), and IL-10 were measured in plasma. Biochemical markers of organ damage, liver NAD+/NADH (indicator of the mitochondrial redox state), plasma nitrate, tissue myeloperoxidase (MPO, indicator of neutrophil accumulation) and malondialdehyde (MDA, indicator of lipid peroxidation), liver and lung chemokines (macrophage inflammatory protein 1alpha [MIP-1alpha ] and MIP-2), and ex vivo vascular reactivity in aortic rings were also measured. Mice treated with inosine had significantly lower levels of circulating cytokines. Organ damage was significantly reduced by inosine treatment, which was associated at the tissue level with an increased hepatic NAD+/NADH ratio, decreased MPO activity in the lung, reduced MDA formation in the gut and liver, and decreased MIP-1alpha and MIP-2 in the lung and liver. Furthermore, inosine significantly improved endothelium-dependent relaxant responses of aortic rings. These effects were associated with significant improvement of the survival of CLP mice treated with inosine, an effect that was still observed when inosine treatment was delayed 1 h after CLP, especially when it was associated with appropriate antibiotic treatment. Thus, inosine reduced systemic inflammation, organ damage, tissue dysoxia, and vascular dysfunction, resulting in improved survival in septic shock.
Original languageEnglish
Pages (from-to)1213-1220
Number of pages8
JournalAmerican Journal of Respiratory and Critical Care Medicine
Volume164
Issue number7
DOIs
Publication statusPublished - Oct 2001

Fingerprint

Inosine
Septic Shock
Punctures
Ligation
Inflammation
NAD
Liver
Chemokine CCL3
Macrophage Inflammatory Proteins
Lung
Blood Vessels
Malondialdehyde
Chemokines
Interleukin-10
Nitrates
Adenosine
Lipid Peroxidation
Peroxidase
Oxidation-Reduction
Endothelium

Cite this

Liaudet, L. ; Mabley, Jon ; Soriano, F.G. ; Pacher, P. ; Marton, A. ; Hasko, G. ; Szabo, C. / Inosine reduces systemic inflammation and improves survival in septic shock induced by cecal ligation and puncture. In: American Journal of Respiratory and Critical Care Medicine. 2001 ; Vol. 164, No. 7. pp. 1213-1220.
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Inosine reduces systemic inflammation and improves survival in septic shock induced by cecal ligation and puncture. / Liaudet, L.; Mabley, Jon; Soriano, F.G.; Pacher, P.; Marton, A.; Hasko, G.; Szabo, C.

In: American Journal of Respiratory and Critical Care Medicine, Vol. 164, No. 7, 10.2001, p. 1213-1220.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Inosine reduces systemic inflammation and improves survival in septic shock induced by cecal ligation and puncture

AU - Liaudet, L.

AU - Mabley, Jon

AU - Soriano, F.G.

AU - Pacher, P.

AU - Marton, A.

AU - Hasko, G.

AU - Szabo, C.

PY - 2001/10

Y1 - 2001/10

N2 - nosine is a naturally occurring purine formed from the breakdown of adenosine. Here we have evaluated the effects of inosine in a murine model of polymicrobial sepsis induced by cecal ligation and puncture (CLP). Mice subjected to CLP were treated with either inosine (100 mg/kg, intraperitoneally) or vehicle 1 h before and 6 h after CLP. After 12 h tumor necrosis factor alpha , interleukin 6 (IL-6), and IL-10 were measured in plasma. Biochemical markers of organ damage, liver NAD+/NADH (indicator of the mitochondrial redox state), plasma nitrate, tissue myeloperoxidase (MPO, indicator of neutrophil accumulation) and malondialdehyde (MDA, indicator of lipid peroxidation), liver and lung chemokines (macrophage inflammatory protein 1alpha [MIP-1alpha ] and MIP-2), and ex vivo vascular reactivity in aortic rings were also measured. Mice treated with inosine had significantly lower levels of circulating cytokines. Organ damage was significantly reduced by inosine treatment, which was associated at the tissue level with an increased hepatic NAD+/NADH ratio, decreased MPO activity in the lung, reduced MDA formation in the gut and liver, and decreased MIP-1alpha and MIP-2 in the lung and liver. Furthermore, inosine significantly improved endothelium-dependent relaxant responses of aortic rings. These effects were associated with significant improvement of the survival of CLP mice treated with inosine, an effect that was still observed when inosine treatment was delayed 1 h after CLP, especially when it was associated with appropriate antibiotic treatment. Thus, inosine reduced systemic inflammation, organ damage, tissue dysoxia, and vascular dysfunction, resulting in improved survival in septic shock.

AB - nosine is a naturally occurring purine formed from the breakdown of adenosine. Here we have evaluated the effects of inosine in a murine model of polymicrobial sepsis induced by cecal ligation and puncture (CLP). Mice subjected to CLP were treated with either inosine (100 mg/kg, intraperitoneally) or vehicle 1 h before and 6 h after CLP. After 12 h tumor necrosis factor alpha , interleukin 6 (IL-6), and IL-10 were measured in plasma. Biochemical markers of organ damage, liver NAD+/NADH (indicator of the mitochondrial redox state), plasma nitrate, tissue myeloperoxidase (MPO, indicator of neutrophil accumulation) and malondialdehyde (MDA, indicator of lipid peroxidation), liver and lung chemokines (macrophage inflammatory protein 1alpha [MIP-1alpha ] and MIP-2), and ex vivo vascular reactivity in aortic rings were also measured. Mice treated with inosine had significantly lower levels of circulating cytokines. Organ damage was significantly reduced by inosine treatment, which was associated at the tissue level with an increased hepatic NAD+/NADH ratio, decreased MPO activity in the lung, reduced MDA formation in the gut and liver, and decreased MIP-1alpha and MIP-2 in the lung and liver. Furthermore, inosine significantly improved endothelium-dependent relaxant responses of aortic rings. These effects were associated with significant improvement of the survival of CLP mice treated with inosine, an effect that was still observed when inosine treatment was delayed 1 h after CLP, especially when it was associated with appropriate antibiotic treatment. Thus, inosine reduced systemic inflammation, organ damage, tissue dysoxia, and vascular dysfunction, resulting in improved survival in septic shock.

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M3 - Article

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SP - 1213

EP - 1220

JO - American Journal of Respiratory and Critical Care Medicine

JF - American Journal of Respiratory and Critical Care Medicine

SN - 1073-449X

IS - 7

ER -