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灯盏花素通过抑制小鼠体内核因子-κB的激活来预防脂多糖诱导的急性肺损伤。

Scutellarin protects against lipopolysaccharide-induced acute lung injury via inhibition of NF-kappaB activation in mice.

作者信息

Tan Zheng-Huai, Yu Ling-Hong, Wei Huai-Ling, Liu Geng-Tao

机构信息

Department of Pharmacology, Institute of Materia Medica, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, China.

出版信息

J Asian Nat Prod Res. 2010 Mar;12(3):175-84. doi: 10.1080/10286020903347906.

Abstract

This paper investigates the effect of natural scutellarin on acute lung injury (ALI) induced by Escherichia coli endotoxin lipopolysaccharide (LPS) in mice and its mechanism of action. Mouse ALI was induced by the injection of LPS (15 mg/kg) via the tail vein, and mice were intraperitoneally injected with 50 and 25 mg/kg of scutellarin before the LPS injection. The lung index, serum NO2(-)/NO3(-), and tumor necrosis factor-alpha (TNF-alpha) levels were determined using kits. The lung lesions were examined by light microscope. The mRNA levels of TNF-alpha, inducible nitric oxide synthase (iNOS), and FasL in pulmonary tissues were detected by RT-PCR. c-Fos, c-Jun, IkappaB, and iNOS proteins were detected by the western blotting method. Pretreatment with 25 and 50 mg/kg of scutellarin significantly reduced lung injury induced by LPS, which expressed in the decrease in lung morphological lesions, serum NO2(-)/NO3(-), TNF-alpha levels, lactate dehydrogenase release, and total protein in the lavage fluid of bronchoalveolar of the lung. The mRNA level of TNF-alpha, iNOS, the protein content of c-Fos, iNOS, and the activation of NF-kappaB in pulmonary tissues were all inhibited, while the lung glutathione level increased. In conclusion, scutellarin has protective action against LPS-induced lung damage in mice, and its underlying mechanism might be the inhibition of IkappaB alpha degradation and the expression of TNF-alpha mRNA.

摘要

本文研究了天然灯盏花素对小鼠大肠杆菌内毒素脂多糖(LPS)诱导的急性肺损伤(ALI)的影响及其作用机制。通过尾静脉注射LPS(15mg/kg)诱导小鼠ALI,并在注射LPS前腹腔注射50mg/kg和25mg/kg的灯盏花素。使用试剂盒测定肺指数、血清NO2(-)/NO3(-)和肿瘤坏死因子-α(TNF-α)水平。通过光学显微镜检查肺损伤情况。采用逆转录聚合酶链反应(RT-PCR)检测肺组织中TNF-α、诱导型一氧化氮合酶(iNOS)和FasL的mRNA水平。采用蛋白质印迹法检测c-Fos、c-Jun、IkappaB和iNOS蛋白。25mg/kg和50mg/kg的灯盏花素预处理可显著减轻LPS诱导的肺损伤,表现为肺形态学损伤、血清NO2(-)/NO3(-)、TNF-α水平、乳酸脱氢酶释放以及肺支气管肺泡灌洗液中总蛋白的降低。肺组织中TNF-α、iNOS的mRNA水平,c-Fos、iNOS的蛋白含量以及NF-κB的激活均受到抑制,而肺谷胱甘肽水平升高。总之,灯盏花素对LPS诱导的小鼠肺损伤具有保护作用,其潜在机制可能是抑制IkappaBα降解和TNF-α mRNA的表达。

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