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Journal Article

Citation

Curtis BJ, Boe DM, Shults JA, Ramirez L, Kovacs EJ. Shock 2019; 51(5): 625-633.

Affiliation

Graduate Program in Immunology, University of Colorado Denver, Anschutz Medical Campus, Aurora, CO 80045.

Copyright

(Copyright © 2019, The Shock Society, Publisher Lippincott Williams and Wilkins)

DOI

10.1097/SHK.0000000000001188

PMID

29846360

Abstract

Burn patients who consumed alcohol prior to injury have worse clinical outcomes, including longer hospital stays, increased ventilator days, and more respiratory infections. Most alcohol consumers are binge drinkers and not chronic alcoholics and binge drinking patterns fluctuate over the week, with consecutive days of drinking over the weekend followed by relative abstinence during the week. We utilized a murine model simulating this drinking pattern in the context of burn injury. Mice were given ethanol for 3 days, rested for 4 days, given ethanol for 3 more days, followed by a sham or 15% total body surface area full-thickness burn. We previously demonstrated that mice exposed to the combined insult exhibited respiratory dysfunction and 50% mortality, with those that succumbed to injury dying between 24 and 72 hours, thus identifying a therapeutic intervention window. Our goal herein is to characterize inflammatory and respiratory parameters during this critical time frame. We saw that mice exposed to the combined insult had the highest circulating and pulmonary cytokine levels at 24 hours, which were normalized by 72 hours in survivors. Alveolar macrophage activation was observed at 24 hours in burned mice, regardless of intoxication (p < 0.05). However, at 72 hours, alveolar macrophages from intoxicated burned mice had elevated CD206, relative to controls (p < 0.05), indicative of an anti-inflammatory phenotype. Taken together, these findings suggest that while lung function and inflammation are normalized by 72 hours, the alterations in alveolar macrophage phenotype shed light on a potential mechanism underlying increased infection susceptibility in intoxicated burn patients.


Language: en

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