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盐酸丙咪嗪对脂多糖诱导的急性肺损伤的保护作用。

Protective effects of imipramine in murine endotoxin-induced acute lung injury.

机构信息

Department of Pulmonary Medicine, Zhongshan Hospital, Shanghai Medical College, Fudan University, Shanghai 200032, China.

出版信息

Eur J Pharmacol. 2010 Jul 25;638(1-3):128-33. doi: 10.1016/j.ejphar.2010.04.005. Epub 2010 Apr 18.

Abstract

The tricyclic antidepressant imipramine has recently emerged as a cytoprotective agent, exerting beneficial effects in inflammatory tissue injury. The present study aimed to investigate therapeutic effects of imipramine in murine model of endotoxin-induced acute lung injury. Mice were administrated intraperitoneally with LPS (lipopolysaccharide) from Escherichia coli or vehicle. Imipramine was administrated intraperitoneally 30 min before LPS challenge. Pretreatment of mice with imipramine reduced lethality. Impramine also significantly attenuated lung inflammation, lung edema, MPO (myeloperoxidase) activity, lung tissue pathological changes and nuclear factor-kappaB DNA binding activity. The results of this study suggest that imipramine can exert protective effects in endotoxin-induced acute lung injury by suppressing nuclear factor-kappaB-mediated expression of inflammatory genes. Thus, imipramine could be a potential novel therapeutic agent for the treatment for acute lung injury.

摘要

三环类抗抑郁药丙咪嗪最近作为一种细胞保护剂出现,在外周组织损伤的炎症中发挥有益作用。本研究旨在探讨丙咪嗪在大肠杆菌内毒素诱导的急性肺损伤小鼠模型中的治疗作用。小鼠腹腔内给予大肠杆菌脂多糖(LPS)或载体。丙咪嗪在 LPS 攻击前 30 分钟腹腔内给药。用丙咪嗪预处理小鼠可降低死亡率。丙咪嗪还显著减轻肺炎症、肺水肿、髓过氧化物酶(MPO)活性、肺组织病理变化和核因子-κB DNA 结合活性。本研究结果表明,丙咪嗪通过抑制核因子-κB 介导的炎症基因表达,在外毒素诱导的急性肺损伤中发挥保护作用。因此,丙咪嗪可能是治疗急性肺损伤的一种有潜力的新型治疗药物。

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