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Induction of lymphocyte apoptosis in a murine model of acute lung injury--modulation by lipid emulsions.

机译:在小鼠诱导淋巴细胞凋亡急性肺损伤模型,由脂质调制乳剂。

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摘要

Acute lung injury (ALI) and sepsis are the major causes of mortality in intensive care units. Lymphocytes apoptosis is a hallmark feature of late detrimental sepsis. Parenteral nutrition in critically ill patients is based on lipid emulsions, but the impact of ALI and lipid emulsions on lymphocytes has not been defined. The effects of intravenously infused conventional soybean oil (SO)-based and new olive oil (OO)-based emulsions on splenic and blood lymphocytes were investigated in a murine model of endotoxin-induced ALI. After LPS challenge and infusion of lipid emulsions, apoptosis of lymphocytes and lung injury were assessed by flow cytometry, Western blot, and histology. Induction of ALI led to a time-dependent decline in splenic and circulating lymphocyte numbers and an increase in apoptosis, with engagement of the extrinsic apoptotic pathway. Both SO- and OO-based emulsions promoted the apoptosis of splenic lymphocytes before induction of ALI. The OO-based emulsions exhibited lower proapoptotic activity than did SO-based emulsions, an observation paralleled by the induction of survival factors. Induction of ALI increased the mortality of mice receiving SO-based emulsions compared with OO-based emulsions and normal saline. Splenic lymphocyte apoptosis is apparent in murine ALI, which may be linked to detrimental outcome. Infusion of lipid emulsions per se provoked splenic lymphocyte apoptosis. Infusion of SO-based emulsions further augmented the apoptosis of splenic and circulating lymphocytes in ALI and led to increased mortality in mice. These findings may be of relevance for patients experiencing ALI that require parenteral nutrition.
机译:急性肺损伤(ALI)和脓毒症是主要的导致死亡的重症监护病房。淋巴细胞凋亡的一个标志性特征有害的脓毒症。危重病人基于脂质乳剂,但阿里和血脂的影响乳剂对淋巴细胞尚未定义。静脉注射注入传统的影响大豆油(所以)的和新的橄榄油(面向对象)的乳剂脾和血淋巴细胞在小鼠模型研究endotoxin-induced阿里。注入脂质乳剂,细胞凋亡淋巴细胞和肺损伤评估流程血细胞计数、免疫印迹和组织学。阿里的导致脾时间下降和淋巴细胞数量和传播在细胞凋亡增加,订婚的外在的凋亡途径。基于面向对象乳剂促进了细胞凋亡脾淋巴细胞诱导ALI之前。基于面向对象乳剂低proapoptotic展出活动基础乳剂相比,一个观察平行的感应生存的因素。死亡率的老鼠接受基础乳剂相比之下,基于面向对象乳剂和正常生理盐水。在小鼠阿里,这可能与有害的结果。激起了脾淋巴细胞凋亡。根据乳剂进一步增强脾细胞凋亡和循环淋巴细胞在阿里和导致小鼠死亡率增加。这些发现可能对患者的相关性经历需要肠外的阿里营养。

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