4.2 Article

Impaired respiratory function and heightened pulmonary inflammation in episodic binge ethanol intoxication and burn injury

Journal

ALCOHOL
Volume 49, Issue 7, Pages 713-720

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.alcohol.2015.06.006

Keywords

Lung; Alcohol; Burn; Plethysmography; Neutrophils; Cytokines

Funding

  1. National Institutes of Health (NIH) [R01 AA012034, R01 GM115257, R21 AA023193, T32 AA013527]
  2. Department of Defense [W81XWH-11-1-0559, F31 AA022566, F32 AA021636, F30 AA022856]
  3. Dr. Ralph and Marian C. Falk Medical Research Trust

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Clinical data indicate that cutaneous burn injuries covering greater than 10% of the total body surface area are associated with significant morbidity and mortality, in which pulmonary complications, including acute respiratory distress syndrome CARDS), contribute to nearly half of all patient deaths. Approximately 50% of burn patients are intoxicated at the time of hospital admission, which increases days on ventilators by 3-fold, and doubles the length of hospitalization, compared to non-intoxicated burn patients. The most common drinking pattern in the United States is binge drinking, where an individual rapidly consumes alcoholic beverages (4 for women, 5 for men) in 2 h. An estimated 38 million Americans binge drink, often several times per month. Experimental data demonstrate that a single binge-ethanol exposure, prior to scald injury, impairs innate and adaptive immune responses, thereby enhancing infection susceptibility and amplifying pulmonary inflammation, neutrophil infiltration, and edema, and is associated with increased mortality. Since these characteristics are similar to those observed in ARDS burn patients, our study objective was to determine whether ethanol intoxication and burn injury and the subsequent pulmonary congestion affect physiological parameters of lung function, using non-invasive and unrestrained plethysmography in a murine model system. Furthermore, to mirror young adult binge-drinking patterns, and to determine the effect of multiple ethanol exposures on pulmonary inflammation, we utilized an episodic binge-ethanol exposure regimen, where mice were exposed to ethanol for a total of 6 days (3 days ethanol, 4 days rest, 3 days ethanol) prior to burn injury. Our analyses demonstrate mice exposed to episodic binge ethanol and burn injury have higher mortality, increased pulmonary congestion and neutrophil infiltration, elevated neutrophil chemoattractants, and respiratory dysfunction, compared to burn or ethanol intoxication alone. Overall, our study identifies plethysmography as a useful tool for characterizing respiratory function in a murine burn model and for future identification of therapeutic compounds capable of restoring pulmonary functionality. (C) 2015 Elsevier Inc. All rights reserved.

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