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山香圆叶总黄酮通过下调炎症信号通路减轻脂多糖诱导的急性肺损伤。

Total flavonoids of Mosla scabra leaves attenuates lipopolysaccharide-induced acute lung injury via down-regulation of inflammatory signaling in mice.

机构信息

Zhejiang Chinese Medical University, Hangzhou 310053, China.

出版信息

J Ethnopharmacol. 2013 Jul 30;148(3):835-41. doi: 10.1016/j.jep.2013.05.020. Epub 2013 Jun 6.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Mosla scabra (Thunb.) C.Y. Wu, belonging to the Labiatae family, is a tomentose and aromatic plant, which is widely used as an antipyretic and antiviral drug for pulmonary diseases and famous for its efficiency in treating colds, fever, pneumonia and chronic bronchitis. To investigate therapeutic effects and possible mechanism of Mosla scabra flavonoids (MF) on lipopolysaccharide (LPS)-induced acute lung injury (ALI) in mice.

MATERIALS AND METHODS

Mice were orally administrated with MF once (30 mg/kg or 90 mg/kg) 1 h before LPS challenge. Lung specimens and the bronchoalveolar lavage fluid (BALF) were isolated for histopathological examinations and biochemical analyses 6 h after LPS challenge.

RESULTS

Pretreatment with MF could decrease significantly lung wet-to-dry weight (W/D) ratio, lower myeloperoxidase (MPO) activity and total protein concentrations in the BALF, reduce serum levels of NO, TNF-α, IL-1β and IL-6 in ALI model. Additionally, MF attenuated lung histopathological changes and significantly inhibited the phosphorylation of p38 MAPK and translocation of NF-κB p65.

CONCLUSIONS

These results showed MF significantly attenuate LPS-induced acute lung injury and production of inflammatory mediators via inhibiting MAPK and NF-κB activation, indicating it as a potential therapeutic agent for ALI.

摘要

民族药理学相关性

石荠苎(Thunb.)C.Y.吴,唇形科植物,是一种多毛和芳香的植物,被广泛用作治疗肺部疾病的解热和抗病毒药物,以治疗感冒、发热、肺炎和慢性支气管炎的功效而闻名。为了研究石荠苎黄酮(MF)对脂多糖(LPS)诱导的急性肺损伤(ALI)的治疗作用及可能的机制。

材料和方法

小鼠在 LPS 攻击前 1 小时口服 MF(30mg/kg 或 90mg/kg)一次。在 LPS 攻击后 6 小时分离肺标本和支气管肺泡灌洗液(BALF)进行组织病理学检查和生化分析。

结果

MF 预处理可显著降低肺湿重/干重(W/D)比值,降低 BALF 中髓过氧化物酶(MPO)活性和总蛋白浓度,降低 ALI 模型中血清中 NO、TNF-α、IL-1β和 IL-6 的水平。此外,MF 减轻了肺组织病理学变化,显著抑制了 p38MAPK 的磷酸化和 NF-κB p65 的易位。

结论

这些结果表明 MF 通过抑制 MAPK 和 NF-κB 的激活,显著减轻 LPS 诱导的急性肺损伤和炎症介质的产生,表明其可能成为治疗 ALI 的一种潜在治疗剂。

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