Literature DB >> 12688540

Effects of age on mortality and antibiotic efficacy in cecal ligation and puncture.

Isaiah R Turnbull1, Joseph J Wlzorek, Dale Osborne, Richard S Hotchkiss, Craig M Coopersmith, Timothy G Buchman.   

Abstract

The incidence and mortality of sepsis increase with age, consequently, 80% of the clinical mortality from sepsis occurs in patients over age 65. Despite this aged clinical population, most research models of sepsis use 6- to 16-week-old mice as patient surrogates. This age range of mice corresponds to human ages 10 to 17 years. To assess the influence of age on rodent CLP and on antibiotic therapy, we studied young (4 month), mature (12 month), and aged (24 month) mice. Male C57BL/6 mice (n = 27-30 in each age group) were subjected to cecal ligation and puncture (CLP), two punctures with a 25-gauge needle. Mice were observed untreated for 10 days. Young mice had 20% mortality, mature mice had 70% mortality (P = 0.0013 vs. young), and aged mice had 75% mortality (P = 0.0001 vs. young). To assess the effects of age on antibiotic therapy, mice were subjected to CLP as above (n = 38-40 in each age group). Mice were then randomized to treatment with intraperitoneal injections of ceftriaxone and metronidazole or normal saline. Therapy was initiated 12 h after CLP, and injections were repeated every 12 h for 7 days. Young mice saw a 56% decrease in mortality from CLP with antibiotic therapy (P = 0.001), and mature mice had a 30% decrease in mortality (P = 0.06). Aged mice saw no benefit from antibiotic therapy. We also compared plasma cytokine levels between young and aged mice after CLP. When compared with young mice, aged mice had higher levels of IL-6 and TNF-alpha 24 h after CLP. However, high IL-6 was predictive of mortality at any age. Mice appear to have age-dependent responses to intra-abdominal sepsis and to appropriate therapy.

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Year:  2003        PMID: 12688540     DOI: 10.1097/00024382-200304000-00003

Source DB:  PubMed          Journal:  Shock        ISSN: 1073-2322            Impact factor:   3.454


  75 in total

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Journal:  Neurobiol Dis       Date:  2011-09-10       Impact factor: 5.996

3.  Effects of Aging on Inflammation and Hemostasis through the Continuum of Critical Illness.

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Journal:  Aging Dis       Date:  2011-12-02       Impact factor: 6.745

4.  Aged mice are unable to mount an effective myeloid response to sepsis.

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Journal:  J Immunol       Date:  2013-12-13       Impact factor: 5.422

5.  Increasing anastomosis safety and preventing abdominal adhesion formation by the use of polypeptides in the rat.

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6.  Reply to "Bacterial Proliferation May Be the Key Component of Sepsis Mortality".

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Journal:  Infect Immun       Date:  2018-10-25       Impact factor: 3.441

7.  Effects of aging on the immunopathologic response to sepsis.

Authors:  Isaiah R Turnbull; Andrew T Clark; Paul E Stromberg; David J Dixon; Cheryl A Woolsey; Christopher G Davis; Richard S Hotchkiss; Timothy G Buchman; Craig M Coopersmith
Journal:  Crit Care Med       Date:  2009-03       Impact factor: 7.598

Review 8.  Bench-to-Bedside: A Translational Perspective on Murine Models of Sepsis.

Authors:  Anthony J Lewis; Matthew R Rosengart
Journal:  Surg Infect (Larchmt)       Date:  2018-02-02       Impact factor: 2.150

9.  Association between lymphotoxin-alpha (tumor necrosis factor-beta) intron polymorphism and predisposition to severe sepsis is modified by gender and age.

Authors:  Eizo Watanabe; Timothy G Buchman; Hiroyuki Hirasawa; Barbara A Zehnbauer
Journal:  Crit Care Med       Date:  2010-01       Impact factor: 7.598

10.  G-protein-coupled receptor kinase-5 mediates inflammation but does not regulate cellular infiltration or bacterial load in a polymicrobial sepsis model in mice.

Authors:  Nandakumar Packiriswamy; Taehyung Lee; Pongali B Raghavendra; Haritha Durairaj; Hongbing Wang; Narayanan Parameswaran
Journal:  J Innate Immun       Date:  2013-03-12       Impact factor: 7.349

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