Schaefer Martina Barbara, Ott Juliane, Mohr Andrea, Bi Ming Hua, Grosz Andrea, Weissmann Norbert, Ishii Satoshi, Grimminger Friedrich, Seeger Werner, Mayer Konstantin
University of Giessen Lung Center (UGLC), Justus-Liebig-University of Giessen, Giessen, Germany.
Crit Care Med. 2007 Feb;35(2):544-54. doi: 10.1097/01.CCM.0000253811.74112.B6.
Cytokines, platelet-activating factor (PAF), and eicosanoids control local and systemic inflammation. Conventional soybean oil-based lipid emulsions used for parenteral nutrition may aggravate the leukocyte inflammatory response or adhesion to the vessel wall. Fish oil-based lipid emulsions, in contrast, may exert an anti-inflammatory effect.
We investigated the impact of lipid emulsions on leukocyte invasion, protein leakage, and cytokines in two murine models of acute inflammation.
Research laboratory of a university hospital.
Wild-type mice and PAF-receptor knockout mice.
Mice received an infusion of normal saline, fish oil- or soybean oil-based lipid emulsions before lipopolysaccharide challenge.
Preinfusion with soybean oil resulted in increased leukocyte invasion, myeloperoxidase activity, and protein leakage and exaggerated release of tumor necrosis factor (TNF)-alpha as well as macrophage inflammatory protein (MIP)-2 into the alveolar space after intratracheal lipopolysaccharide challenge. In contrast, preinfusion with fish oil reduced leukocyte invasion, myeloperoxidase activity, protein leakage, and TNF-alpha as well as MIP-2 generation. Corresponding profiles were found in plasma following intraperitoneal lipopolysaccharide application: Soybean oil increased but fish oil decreased the TNF-alpha and MIP-2 formation. When PAF-receptor-deficient mice were challenged with lipopolysaccharide, leukocyte invasion, lung tissue myeloperoxidase, cytokine generation, and alveolar protein leakage corresponded to those observed in wild-type animals. Fish oil and soybean oil lost their diverging effects on leukocyte transmigration, myeloperoxidase activity, leakage response, and cytokine generation in these knockout mice. Similarly, the differential impact of both lipid emulsions on these lipopolysaccharide-provoked changes was suppressed after pretreating animals with a PAF-receptor antagonist.
Fish oil- vs. soybean oil-based lipid infusions exert anti- vs. proinflammatory effects in murine models of acute inflammation. The PAF/PAF-receptor-linked signaling appears to be a prerequisite for this differential profile.
细胞因子、血小板活化因子(PAF)和类花生酸控制局部和全身炎症。用于肠外营养的传统大豆油基脂质乳剂可能会加重白细胞炎症反应或对血管壁的黏附。相比之下,鱼油基脂质乳剂可能具有抗炎作用。
我们在两种急性炎症小鼠模型中研究了脂质乳剂对白细胞浸润、蛋白质渗漏和细胞因子的影响。
大学医院的研究实验室。
野生型小鼠和PAF受体基因敲除小鼠。
小鼠在接受脂多糖攻击前输注生理盐水、鱼油基或大豆油基脂质乳剂。
气管内给予脂多糖攻击后,预先输注大豆油会导致白细胞浸润增加、髓过氧化物酶活性增强、蛋白质渗漏以及肿瘤坏死因子(TNF)-α和巨噬细胞炎性蛋白(MIP)-2向肺泡腔的过度释放。相比之下,预先输注鱼油可减少白细胞浸润、髓过氧化物酶活性、蛋白质渗漏以及TNF-α和MIP-2的生成。腹腔内给予脂多糖后,血浆中也发现了相应的变化:大豆油会增加但鱼油会减少TNF-α和MIP-2的形成。当用脂多糖攻击PAF受体缺陷小鼠时,白细胞浸润、肺组织髓过氧化物酶、细胞因子生成和肺泡蛋白渗漏与野生型动物中观察到的情况相似。在这些基因敲除小鼠中,鱼油和大豆油对白细胞迁移、髓过氧化物酶活性、渗漏反应和细胞因子生成的不同影响消失。同样,在用PAF受体拮抗剂预处理动物后,两种脂质乳剂对这些脂多糖引起的变化的差异影响也被抑制。
在急性炎症小鼠模型中,鱼油基与大豆油基脂质输注分别发挥抗炎和促炎作用。PAF/PAF受体相关信号似乎是这种差异表现的先决条件。