COMPARISON OF THE EFFECTS OF AGING AND IL-6 ON THE HEPATIC INFLAMMATORY RESPONSE IN TWO MODELS OF SYSTEMIC INJURY
- 1 February 2009
- journal article
- basic science-aspects
- Published by Wolters Kluwer Health in Shock
- Vol. 31 (2) , 178-184
- https://doi.org/10.1097/shk.0b013e318180feb8
Abstract
Regardless of age, a marked elevation in circulating IL-6 levels correlates with increased mortality after injury or an inflammatory challenge. We previously reported that aged IL-6 knockout mice given LPS have improved survival and reduced inflammatory response than LPS-treated aged wild type (WT) mice. Herein, we analyzed the effects of aging and IL-6 on the hepatic inflammatory response in two models of systemic injury: dorsal scald (burn) injury versus intraperitoneal LPS administration. At 24 h after burn injury, circulating alanine aminotransferase and hepatic neutrophil accumulation were comparable regardless of age or IL-6 deficiency. However, at this same time point, these indicators of liver damage, in addition to hepatic levels of KC, a neutrophil chemoattractant, were increased in aged WT mice given LPS relative to young WT mice given LPS. The hepatic injury was drastically reduced in aged IL-6 knockout mice given LPS as compared with LPS-exposed aged WT mice. Our results suggest that the nature of the insult will determine the degree of remote injury in aged animals. In addition, the role of IL-6 as a contributing factor of tissue injury may be insult specific. ABBREVIATIONS-ALT-Alanine aminotransferase; MIP-2-macrophage inflammatory protein 2; MOF-multiple organ failure; MPO-myeloperoxidase; TBSA-total body surface areaKeywords
This publication has 36 references indexed in Scilit:
- An age-associated increase in pulmonary inflammation after burn injury is abrogated by CXCR2 inhibitionJournal of Leukocyte Biology, 2008
- Characterization of a lipopolysaccharide mediated neutrophilic hepatitis model in Sprague Dawley ratsJournal of Applied Toxicology, 2007
- Advanced age exacerbates the pulmonary inflammatory response after lipopolysaccharide exposureCritical Care Medicine, 2007
- The Early Acute Phase Response After Burn Injury in MiceJournal of Burn Care & Research, 2007
- MOF, MODS, AND SIRSShock, 2006
- The Molecular Inflammatory Process in AgingAntioxidants and Redox Signaling, 2006
- Linking the “two-hit” response following injury to enhanced TLR4 reactivityJournal of Leukocyte Biology, 2004
- Critical role of CXC chemokines in endotoxemic liver injury in miceJournal of Leukocyte Biology, 2003
- Aging‐induced proinflammatory shift in cytokine expression profile in rat coronary arteriesThe FASEB Journal, 2003
- Clinical analysis of multiple organ failure in burned patientsBurns, 1987