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Correlation of measurable serum markers of inflammation with lung levels following bilateral femur fracture in a rat model

INTRODUCTION: Evaluation of the systemic inflammatory status following major orthopedic trauma has become an important adjunct in basing post-injury clinical decisions. In the present study, we examined the correlation of serum and lung inflammatory marker levels following bilateral femur fracture....

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Autores principales: Sears, Benjamin W, Volkmer, Dustin, Yong, Sherri, Himes, Ryan D, Lauing, Kristen, Morgan, Michele, Stover, Michael D, Callaci, John J
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3062967/
https://www.ncbi.nlm.nih.gov/pubmed/21442011
http://dx.doi.org/10.2147/JIR.S12853
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author Sears, Benjamin W
Volkmer, Dustin
Yong, Sherri
Himes, Ryan D
Lauing, Kristen
Morgan, Michele
Stover, Michael D
Callaci, John J
author_facet Sears, Benjamin W
Volkmer, Dustin
Yong, Sherri
Himes, Ryan D
Lauing, Kristen
Morgan, Michele
Stover, Michael D
Callaci, John J
author_sort Sears, Benjamin W
collection PubMed
description INTRODUCTION: Evaluation of the systemic inflammatory status following major orthopedic trauma has become an important adjunct in basing post-injury clinical decisions. In the present study, we examined the correlation of serum and lung inflammatory marker levels following bilateral femur fracture. MATERIALS AND METHODS: 45 Sprague Dawley rats underwent sham operation or bilateral femoral intramedullary pinning and mid-diaphyseal closed fracture via blunt guillotine. Animals were euthanized at specific time points after injury. Serum and lung tissue were collected, and 24 inflammatory markers were analyzed by immunoassay. Lung histology was evaluated by a blinded pathologist. RESULTS: Bilateral femur fracture significantly increased serum markers of inflammation including interleukin (IL)-2, IL-6, IL-10, GM-CSF, KC/GRO, MCP-1, and WBC. Femur fracture significantly increased serum and lung levels of IL-1a and KC/GRO at 6 hours. Lung levels of IL-6 demonstrated a trend towards significance. Histologic changes in pulmonary tissue after fracture included pulmonary edema and bone elements including cellular hematopoietic cells, bone fragments and marrow emboli. DISCUSSION AND CONCLUSION: Our results indicate that bilateral femur fracture with fixation in rats results in increases in serum markers of inflammation. Among the inflammatory markers measured, rise in the serum KC/GRO (CINC-1), a homolog to human IL-8, correlated with elevated levels of lung KC/GRO. Ultimately, analysis of serum levels of KC/GRO (CINC-1), or human IL-8, may be a useful adjunct to guide clinical decisions regarding surgical timing.
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spelling pubmed-30629672011-03-23 Correlation of measurable serum markers of inflammation with lung levels following bilateral femur fracture in a rat model Sears, Benjamin W Volkmer, Dustin Yong, Sherri Himes, Ryan D Lauing, Kristen Morgan, Michele Stover, Michael D Callaci, John J J Inflamm Res Original Research INTRODUCTION: Evaluation of the systemic inflammatory status following major orthopedic trauma has become an important adjunct in basing post-injury clinical decisions. In the present study, we examined the correlation of serum and lung inflammatory marker levels following bilateral femur fracture. MATERIALS AND METHODS: 45 Sprague Dawley rats underwent sham operation or bilateral femoral intramedullary pinning and mid-diaphyseal closed fracture via blunt guillotine. Animals were euthanized at specific time points after injury. Serum and lung tissue were collected, and 24 inflammatory markers were analyzed by immunoassay. Lung histology was evaluated by a blinded pathologist. RESULTS: Bilateral femur fracture significantly increased serum markers of inflammation including interleukin (IL)-2, IL-6, IL-10, GM-CSF, KC/GRO, MCP-1, and WBC. Femur fracture significantly increased serum and lung levels of IL-1a and KC/GRO at 6 hours. Lung levels of IL-6 demonstrated a trend towards significance. Histologic changes in pulmonary tissue after fracture included pulmonary edema and bone elements including cellular hematopoietic cells, bone fragments and marrow emboli. DISCUSSION AND CONCLUSION: Our results indicate that bilateral femur fracture with fixation in rats results in increases in serum markers of inflammation. Among the inflammatory markers measured, rise in the serum KC/GRO (CINC-1), a homolog to human IL-8, correlated with elevated levels of lung KC/GRO. Ultimately, analysis of serum levels of KC/GRO (CINC-1), or human IL-8, may be a useful adjunct to guide clinical decisions regarding surgical timing. Dove Medical Press 2010-08-26 /pmc/articles/PMC3062967/ /pubmed/21442011 http://dx.doi.org/10.2147/JIR.S12853 Text en © 2010 Sears et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Sears, Benjamin W
Volkmer, Dustin
Yong, Sherri
Himes, Ryan D
Lauing, Kristen
Morgan, Michele
Stover, Michael D
Callaci, John J
Correlation of measurable serum markers of inflammation with lung levels following bilateral femur fracture in a rat model
title Correlation of measurable serum markers of inflammation with lung levels following bilateral femur fracture in a rat model
title_full Correlation of measurable serum markers of inflammation with lung levels following bilateral femur fracture in a rat model
title_fullStr Correlation of measurable serum markers of inflammation with lung levels following bilateral femur fracture in a rat model
title_full_unstemmed Correlation of measurable serum markers of inflammation with lung levels following bilateral femur fracture in a rat model
title_short Correlation of measurable serum markers of inflammation with lung levels following bilateral femur fracture in a rat model
title_sort correlation of measurable serum markers of inflammation with lung levels following bilateral femur fracture in a rat model
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3062967/
https://www.ncbi.nlm.nih.gov/pubmed/21442011
http://dx.doi.org/10.2147/JIR.S12853
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