Improved Survival of TNF-Deficient Mice During the Zymosan-Induced Multiple Organ Dysfunction Syndrome
- 1 June 2002
- journal article
- research article
- Published by Wolters Kluwer Health in Shock
- Vol. 17 (6) , 468-472
- https://doi.org/10.1097/00024382-200206000-00005
Abstract
The purpose of the study was to investigate the course of the zymosan-induced multiple organ dysfunction syndrome (MODS) in the absence of tumor necrosis factor (TNF) in a murine model. Tumor Necrosis Factor-α-lymphotoxin-α knockout (TNF/LT−/−) mice (n = 36) and wild-type (TNF/LT+/+) mice (n = 36) received 40 μg of lipopolysaccharide (LPS) intraperitoneally followed by zymosan at a dose of 1 mg/g body weight 6 days later (day 0). Animals were monitored daily for body weight and temperature and clinical symptoms. At day 22, most of the surviving mice were killed to examine organ weight and histology. A small number of animals were followed until day 48. In all animals, zymosan induced an acute sterile peritonitis phase followed by an apparent recovery. From day 8 onwards the TNF/LT+/+ mice entered a third—MODS-like—phase, characterized by loss of body weight, decreased body temperature, and significant mortality. At day 22, survival in the TNF/LT−/− mice (92%) was significantly (P = 0.01) higher than in the TNF/LT+/+ mice (60%). In addition, average body temperature and average relative (vs. weight at day 0) body weight were higher in the TNF/LT−/− mice than in the TNF/LT+/+ mice (35.9°C and 100% vs. 33.3°C and 84%, respectively). However, at this time point, surviving animals from both groups showed similar and significant organ damage, indicated by an increase in absolute and relative (vs body weight) weight of lung, spleen, and liver (liver only in the TNF/LT−/− mice). Moreover, histopathological examination of organs from the surviving animals showed a similar degree of microscopic damage in both groups. Interestingly, besides mononuclear cells, inflammatory infiltrates in lungs and livers of TNF/LT+/+ but not of TNF−/− mice contained neutrophils. In conclusion, TNF-deficient mice exhibit significantly improved morbidity and mortality during zymosan-induced MODS. However, the absence of TNF does not completely protect against MODS in this murine model.Keywords
This publication has 32 references indexed in Scilit:
- ELUCIDATION OF THE EARLY EVENTS CONTRIBUTING TO ZYMOSAN-INDUCED MULTIPLE ORGAN DYSFUNCTION SYNDROME USING MIP-1α, C3 KNOCKOUT, AND C5-DEFICIENT MICEShock, 1999
- SYSTEMIC INFLAMMATORY RESPONSE SYNDROME (SIRS), MULTIPLE ORGAN DYSFUNCTION SYNDROME (MODS), MULTIPLE ORGAN FAILURE (MOF)Shock, 1998
- Mice heterozygous for a deletion of the tumor necrosis factor‐α and lymphotoxin‐α genes: biological importance of a nonlinear response of tumor necrosis factor‐α to gene dosageEuropean Journal of Immunology, 1997
- Inflammatory cytokines in an experimental model for the multiple organ dysfunction syndromeCritical Care Medicine, 1996
- Toward a theory regarding the pathogenesis of the systemic inflammatory response syndromeCritical Care Medicine, 1996
- Tumor Necrosis Factor: Function, Release and ClearanceCritical Reviews in Immunology, 1996
- Deficiency of complement factor C5 reduces early mortality but does not prevent organ damage in an animal model of multiple organ dysfunction syndromeCritical Care Medicine, 1995
- VOLATILE ANESTHETIC MODULATION OF LUNG INJURY AND OUTCOME IN A MURINE MODEL OF MULTIPLE ORGAN DYSFUNCTION SYNDROMEShock, 1995
- Neutrophil-mediated tissue injury and its modulationIntensive Care Medicine, 1995
- Multiple Organ Failure Pathophysiology and Potential Future TherapyAnnals of Surgery, 1992