首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Plasma and lipids from stored packed red blood cells cause acute lung injury in an animal model.
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Plasma and lipids from stored packed red blood cells cause acute lung injury in an animal model.

机译:在动物模型中储存的堆积红细胞中的血浆和脂质会导致急性肺损伤。

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摘要

Transfusion-related acute lung injury (TRALI) is a serious complication of hemotherapy. During blood storage, lipids are generated and released into the plasma. In this study, the role of these lipids in TRALI was investigated using an isolated, perfused rat lung model. Rats were pretreated with endotoxin (LPS) or saline in vivo and the lungs were isolated, ventilated, and perfused with saline, or (a) 5% (vol/ vol) fresh human plasma, (b) plasma from stored blood from the day of isolation (D.0) or from the day of outdate (D.42), (c) lipid extracts from D.42 plasma, or (d) purified lysophosphatidylcholines. Lungs from saline or LPS-pretreated rats perfused with fresh (D.0) plasma showed no pulmonary damage as compared with saline perfused controls. LPS pretreatment/D.42 plasma perfusion caused acute lung injury (ALI) manifested by dramatic changes in both pulmonary artery pressure and edema. Incubation of LPS pre-tx rats with mibefradil, a Ca2+ channel blocker, or WEB 2170, a platelet-activating factor (PAF) receptor antagonist, inhibited ALI caused by D.42 plasma. Lung histology showed neutrophil sequestration without ALI with LPS pretreatment/saline or D.0 plasma perfusion, but ALI with LPS pretreatment/D.42 plasma perfusion, and inhibition of D.42 plasma induced ALI with WEB 2170 or mibefradil. A significant increase in leukotriene E4 was present in LPS-pretreated/D.42 plasma-perfused lungs that was inhibited by WEB 2170. Lastly, significant pulmonary edema was produced when lipid extracts of D.42 plasma or lysophosphatidylcholines were perfused into LPS-pretreated lungs. Lipids caused ALI without vasoconstriction, except at the highest dose employed. In conclusion, both plasma and lipids from stored blood produced pulmonary damage in a model of acute lung injury. TRALI, like the adult respiratory distress syndrome, may be the result of two insults: one derived from stored blood and the other from the clinical condition of the patient.
机译:输血相关的急性肺损伤(TRALI)是血液治疗的严重并发症。在血液存储过程中,会产生脂质并将其释放到血浆中。在这项研究中,使用分离的灌注大鼠肺模型研究了这些脂质在TRALI中的作用。在体内对大鼠进行内毒素(LPS)或生理盐水预处理,并用生理盐水或(a)5%(vol / vol)新鲜人血浆,(b)从当天起储存的血浆中分离,通气并灌注肺分离(D.0)或从过期日期(D.42)开始,(c)来自D.42血浆的脂质提取物,或(d)纯化的溶血磷脂酰胆碱。与盐水对照组相比,盐水或经LPS预处理的大鼠的新鲜(D.0)血浆灌注的肺未显示肺损伤。 LPS预处理/D.42血浆灌注引起的急性肺损伤(ALI),表现为肺动脉压和水肿的急剧变化。 LPS pre-tx大鼠与米贝拉地尔,Ca2 +通道阻滞剂或WEB 2170(血小板活化因子(PAF)受体拮抗剂)一起孵育可抑制D.42血浆引起的ALI。肺组织学检查显示,没有LPS预处理/生理盐水或D.0血浆灌注的ALI,中性粒细胞隔离,但LPS预处理/D.42血浆灌注的ALI,以及用WEB 2170或咪贝地尔对D.42血浆诱导的ALI的抑制作用。经LPS预处理/D.42血浆灌注的肺中白三烯E4的显着增加,被WEB 2170抑制。最后,当将LPS预处理的D.42血浆或溶血磷脂酰胆碱的脂质提取物灌注时,会产生明显的肺水肿。肺。脂质引起的ALI没有血管收缩,除非使用最高剂量。总之,在急性肺损伤模型中,血浆和血脂都产生了肺损伤。就像成人呼吸窘迫综合征一样,TRALI可能是两种侮辱的结果:一种是来自血液储备,另一种是来自患者的临床状况。

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