Propofol Prevents Lung Injury Following Intestinal Ischemia-Reperfusion

被引:46
|
作者
Vasileiou, Ioanna [2 ]
Kalimeris, Konstantinos [1 ]
Nomikos, Tzortzis [3 ]
Xanthopoulou, Marianna N. [3 ]
Perrea, Despoina [2 ]
Agrogiannis, George [4 ]
Nakos, George [5 ]
Kostopanagiotou, Georgia [1 ]
机构
[1] Univ Athens, Sch Med, Dept Anesthesiol 2, Attikon Hosp, Athens 12462, Greece
[2] Laikon Gen Hosp, Expt Surg Lab, Athens, Greece
[3] Harokopio Univ, Dept Sci Nutr Dietet, Athens, Greece
[4] Univ Athens, Sch Med, Natl & Kapodistrian Univ Athens, Dept Pathol 1, Athens 12462, Greece
[5] Univ Ioannina, Univ Hosp, Intens Care Unit, GR-45110 Ioannina, Greece
关键词
intestinal ischemia-reperfusion; lung injury; oxidative stress; propofol; surfactant; RESPIRATORY-DISTRESS-SYNDROME; SURFACTANT LIPIDS; RAT MODEL; ANESTHESIA; INFLAMMATION; MACROPHAGES; LEUKOCYTES; CLEARANCE; ENDOTOXIN; LIVER;
D O I
10.1016/j.jss.2010.07.034
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background. The antioxidant properties of propofol have been shown to improve ischemia/reperfusion injury. We investigated whether anesthesia with propofol can ameliorate remote lung injury induced by intestinal ischemia-reperfusion (IIR). Materials and Methods. Thirty male Wistar rats were randomly allocated in three groups (n = 10 each): animals in group Sham were anesthetized with ketamine and xylazine and then laparotomy and sham IIR followed. Animals in group IIR received ketamine and xylazine and were then subjected to clamping of the superior mesenteric artery for 45 min and reperfusion for 4 h. Group IIR + P received anesthesia with propofol and then IIR was induced, as in group IIR. Blood samples for blood gases and malondialdehyde measurements were drawn at the end of reperfusion. Bronchoalveolar lavage fluid (BALF) was obtained to measure cell counts, total protein, and phospholipids levels. Results. Induction of IIR resulted in deteriorated oxygenation, acidemia, and inflammatory cells sequestration, along with increased BALF protein content and increased proportions of small surfactant aggregates. Anesthesia with propofol alleviated intestinal injury and efficiently prevented lipid oxidation. In group IIR + P inflammatory cell infiltration and pulmonary histologic changes were significantly limited. The increase in BALF total protein and the changes in surfactant aggregates were prevented, leading to normal systemic oxygenation. Conclusion. Using propofol to induce and maintain anesthesia efficiently prevented IIR-induced lung injury. Systemic antioxidant protection, improvement of intestinal injury, inhibition of the inflammatory response, and preservation of the alveolar-capillary permeability seem to be crucial mediating mechanisms for this simple and clinically relevant intervention. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:146 / 152
页数:7
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