Old Mice Demonstrate Organ Dysfunction as well as Prolonged Inflammation, Immunosuppression, and Weight Loss in a Modified Surgical Sepsis Model.

OBJECTIVES Our goal was to "reverse translate" the human response to surgical sepsis into the mouse by modifying a widely adopted murine intra-abdominal sepsis model to engender a phenotype that conforms to current sepsis definitions and follows the most recent expert recommendations for animal preclinical sepsis research. Furthermore, we aimed to create a model that allows the study of aging on the long-term host response to sepsis. DESIGN Experimental study. SETTING Research laboratory. SUBJECTS Young (3-5 mo) and old (18-22 mo) C57BL/6j mice. INTERVENTIONS Mice received no intervention or were subjected to polymicrobial sepsis with cecal ligation and puncture followed by fluid resuscitation, analgesia, and antibiotics. Subsets of mice received daily chronic stress after cecal ligation and puncture for 14 days. Additionally, modifications were made to ensure that "Minimum Quality Threshold in Pre-Clinical Sepsis Studies" recommendations were followed. MEASUREMENTS AND MAIN RESULTS Old mice exhibited increased mortality following both cecal ligation and puncture and cecal ligation and puncture + daily chronic stress when compared with young mice. Old mice developed marked hepatic and/or renal dysfunction, supported by elevations in plasma aspartate aminotransferase, blood urea nitrogen, and creatinine, 8 and 24 hours following cecal ligation and puncture. Similar to human sepsis, old mice demonstrated low-grade systemic inflammation 14 days after cecal ligation and puncture + daily chronic stress and evidence of immunosuppression, as determined by increased serum concentrations of multiple pro- and anti-inflammatory cytokines and chemokines when compared with young septic mice. In addition, old mice demonstrated expansion of myeloid-derived suppressor cell populations and sustained weight loss following cecal ligation and puncture + daily chronic stress, again similar to the human condition. CONCLUSIONS The results indicate that this murine cecal ligation and puncture + daily chronic stress model of surgical sepsis in old mice adhered to current Minimum Quality Threshold in Pre-Clinical Sepsis Studies guidelines and met Sepsis-3 criteria. In addition, it effectively created a state of persistent inflammation, immunosuppression, and weight loss, thought to be a key aspect of chronic sepsis pathobiology and increasingly more prevalent after human sepsis.

[1]  C. Deutschman,et al.  Premise for Standardized Sepsis Models. , 2019, Shock.

[2]  M. Singer,et al.  Correction to: Minimum Quality Threshold in Pre-Clinical Sepsis Studies (MQTiPSS): an international expert consensus initiative for improvement of animal modeling in sepsis , 2018, Infection.

[3]  M. Singer,et al.  Minimum Quality Threshold in Pre-Clinical Sepsis Studies (MQTiPSS): an international expert consensus initiative for improvement of animal modeling in sepsis , 2018, Infection.

[4]  M. Singer,et al.  Minimum quality threshold in pre-clinical sepsis studies (MQTiPSS): an international expert consensus initiative for improvement of animal modeling in sepsis , 2018, Intensive Care Medicine Experimental.

[5]  B. Brumback,et al.  The impact of age on the innate immune response and outcomes after severe sepsis/septic shock in trauma and surgical intensive care unit patients , 2018, The journal of trauma and acute care surgery.

[6]  H. Ueno,et al.  Innate Immunity in the Persistent Inflammation, Immunosuppression, and Catabolism Syndrome and Its Implications for Therapy , 2018, Front. Immunol..

[7]  M. Giacca,et al.  The innate immune system in chronic cardiomyopathy: a European Society of Cardiology (ESC) scientific statement from the Working Group on Myocardial Function of the ESC , 2018, European journal of heart failure.

[8]  B. Brumback,et al.  Benchmarking clinical outcomes and the immunocatabolic phenotype of chronic critical illness after sepsis in surgical intensive care unit patients , 2017, The journal of trauma and acute care surgery.

[9]  M. Kaneki Metabolic Inflammatory Complex in Sepsis: Septic Cachexia as a Novel Potential Therapeutic Target , 2017, Shock.

[10]  M. C. Machado,et al.  Septic Shock and the Aging Process: A Molecular Comparison , 2017, Front. Immunol..

[11]  B. Brumback,et al.  Evidence for Persistent Immune Suppression in Patients Who Develop Chronic Critical Illness After Sepsis , 2017, Shock.

[12]  Lynne U. Sneddon,et al.  Considering aspects of the 3Rs principles within experimental animal biology , 2017, Journal of Experimental Biology.

[13]  V. Nomellini,et al.  A Murine Model of Persistent Inflammation, Immune Suppression, and Catabolism Syndrome , 2017, International journal of molecular sciences.

[14]  L. Moldawer,et al.  Murine Models of Sepsis and Trauma: Can We Bridge the Gap? , 2017, ILAR journal.

[15]  B. Brumback,et al.  Sepsis and Critical Illness Research Center investigators: protocols and standard operating procedures for a prospective cohort study of sepsis in critically ill surgical patients , 2017, BMJ Open.

[16]  H. Saito,et al.  Late Therapeutic Intervention with Antibiotics and Fluid Resuscitation Allows for a Prolonged Disease Course with High Survival in a Severe Murine Model of Sepsis , 2017, Shock.

[17]  M. Singer,et al.  Sequential Analysis of a Panel of Biomarkers and Pathologic Findings in a Resuscitated Rat Model of Sepsis and Recovery , 2017, Critical care medicine.

[18]  B. Brumback,et al.  Human Myeloid-derived Suppressor Cells are Associated With Chronic Immune Suppression After Severe Sepsis/Septic Shock , 2017, Annals of surgery.

[19]  L. Moldawer,et al.  Persistent Inflammation, Immunosuppression and Catabolism Syndrome. , 2017, Critical care clinics.

[20]  Rana H. Bachir,et al.  Are patients with cancer with sepsis and bacteraemia at a higher risk of mortality? A retrospective chart review of patients presenting to a tertiary care centre in Lebanon , 2017, BMJ Open.

[21]  Sangeeta Mehta,et al.  Surviving Sepsis Campaign: International Guidelines for Management of Sepsis and Septic Shock: 2016 , 2017, Intensive Care Medicine.

[22]  C. Aldecoa,et al.  Sepsis and Immunosenescence in the Elderly Patient: A Review , 2017, Front. Med..

[23]  M. Younis,et al.  Hospital-related cost of sepsis: A systematic review. , 2017, The Journal of infection.

[24]  L. Moldawer,et al.  Sepsis Pathophysiology, Chronic Critical Illness, and Persistent Inflammation-Immunosuppression and Catabolism Syndrome , 2017, Critical care medicine.

[25]  S. Opal,et al.  Long-Term Quality of Life Among Survivors of Severe Sepsis: Analyses of Two International Trials* , 2016, Critical care medicine.

[26]  Pallav Sengupta,et al.  Men and mice: Relating their ages. , 2016, Life sciences.

[27]  C. Coopersmith,et al.  Murine Lung Cancer Increases CD4+ T Cell Apoptosis and Decreases Gut Proliferative Capacity in Sepsis , 2016, PloS one.

[28]  Christopher W Seymour,et al.  Developing a New Definition and Assessing New Clinical Criteria for Septic Shock: For the Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3). , 2016, JAMA.

[29]  L. Moldawer,et al.  The future of murine sepsis and trauma research models , 2015, Journal of leukocyte biology.

[30]  H. Baker,et al.  A Detailed Characterization of the Dysfunctional Immunity and Abnormal Myelopoiesis Induced by Severe Shock and Trauma in the Aged , 2015, The Journal of Immunology.

[31]  P. King,et al.  Inflammation in chronic obstructive pulmonary disease and its role in cardiovascular disease and lung cancer , 2015, Clinical and Translational Medicine.

[32]  A. Mohr,et al.  Chronic restraint stress after injury and shock is associated with persistent anemia despite prolonged elevation in erythropoietin levels , 2015, The journal of trauma and acute care surgery.

[33]  M. Baldwin,et al.  Measuring and predicting long-term outcomes in older survivors of critical illness. , 2015, Minerva anestesiologica.

[34]  M. Balas,et al.  Understanding and Reducing Disability in Older Adults Following Critical Illness* , 2015, Critical care medicine.

[35]  K. Simpson,et al.  Frequency, Cost, and Risk Factors of Readmissions Among Severe Sepsis Survivors* , 2015, Critical care medicine.

[36]  H. Baker,et al.  Advanced age is associated with worsened outcomes and a unique genomic response in severely injured patients with hemorrhagic shock , 2015, Critical Care.

[37]  G. Escobar,et al.  Hospital deaths in patients with sepsis from 2 independent cohorts. , 2014, JAMA.

[38]  R. Bellomo,et al.  Mortality related to severe sepsis and septic shock among critically ill patients in Australia and New Zealand, 2000-2012. , 2014, JAMA.

[39]  H. Baker,et al.  Aged Mice Are Unable To Mount an Effective Myeloid Response to Sepsis , 2014, The Journal of Immunology.

[40]  A. Levine,et al.  Chronic restraint stress attenuates p53 function and promotes tumorigenesis , 2012, Proceedings of the National Academy of Sciences.

[41]  R. Star,et al.  Chronic kidney disease worsens sepsis and sepsis-induced acute kidney injury by releasing High Mobility Group Box Protein-1. , 2011, Kidney international.

[42]  G. Kumar,et al.  Nationwide trends of severe sepsis in the 21st century (2000-2007). , 2011, Chest.

[43]  Arthur S Slutsky,et al.  An official American Thoracic Society workshop report: features and measurements of experimental acute lung injury in animals. , 2011, American journal of respiratory cell and molecular biology.

[44]  L. C. Pôrto,et al.  Cutaneous wound healing of chronically stressed mice is improved through catecholamines blockade , 2010, Experimental dermatology.

[45]  M. Dünser,et al.  Macroscopic Postmortem Findings in 235 Surgical Intensive Care Patients with Sepsis , 2009, Anesthesia and analgesia.

[46]  C. Coopersmith,et al.  Effects of aging on the immunopathologic response to sepsis , 2009, Critical care medicine.

[47]  W. O'Neill,et al.  Age-Related Hearing Loss in C57BL/6J Mice has both Frequency-Specific and Non-Frequency-Specific Components that Produce a Hyperacusis-Like Exaggeration of the Acoustic Startle Reflex , 2007, Journal of the Association for Research in Otolaryngology.

[48]  Huan Yang,et al.  Chronic Sepsis Mortality Characterized by an Individualized Inflammatory Response1 , 2007, The Journal of Immunology.

[49]  G. Pawelec,et al.  Aging and innate immunity. , 2006, Immunity.

[50]  Marc Moss,et al.  The effect of age on the development and outcome of adult sepsis* , 2006, Critical care medicine.

[51]  F. Dhabhar,et al.  Modulation of natural killer cell activity by restraint stress during an influenza A/PR8 infection in mice , 2004, Brain, Behavior, and Immunity.

[52]  C. Coopersmith,et al.  Effects of Age on Mortality and Antibiotic Efficacy in Cecal Ligation and Puncture , 2003, Shock.

[53]  G. Clermont,et al.  Epidemiology of severe sepsis in the United States: Analysis of incidence, outcome, and associated costs of care , 2001, Critical care medicine.

[54]  M. Swain,et al.  Environmental stress-induced gastrointestinal permeability is mediated by endogenous glucocorticoids in the rat. , 2000, Gastroenterology.

[55]  M. Edwards,et al.  Enhanced susceptibility of mice with streptozotocin-induced diabetes to type II group B streptococcal infection , 1983, Infection and immunity.

[56]  Y. Kitahara,et al.  Reduced resistance to Pseudomonas septicaemia in diabetic mice. , 1981, Clinical and experimental immunology.

[57]  L. Cassis,et al.  Measuring Blood Pressure Using a Noninvasive Tail Cuff Method in Mice. , 2017, Methods in molecular biology.