焦梅谷抗脂多糖致小鼠急性肺损伤活性物质的UHPLC-MS分析。

IF 3.2 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Dan Zhou, Kai He, Wei Cai, Bin Li, Zaiqi Zhang
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引用次数: 0

摘要

目的:鉴定侗族典型中草药焦美谷(Cayratia albifolia C.L.Li)的抗炎成分并揭示其作用机制。方法:首次采用超高效液相色谱-四极静电场轨道阱质谱(UHPLC-Q-Exactive Orbitrap MS)对抗炎活性最高的JMG乙酸乙酯提取物进行化学成分分析。采用脂多糖(LPS)诱导的RAW 264.7细胞模型和脂多糖(10 mg/kg)诱导的BALB/c小鼠急性肺损伤模型,研究JMG提取物的抗炎活性及其机制。主要发现:共鉴定出木脂素、芹菜素、槲皮素、金菊素、苯连菌素、戊二醇等65种化合物。在200 mg/kg剂量下,JMG乙酸乙酯提取物可逆转lps诱导的急性肺损伤模型肺泡结构变化和炎症细胞浸润。与LPS组比较,200 mg/kg jmg组大鼠血清中IL-1β、IL-6和TNF-α水平分别降低58.6%、56.5%和87.6%。Western blot结果显示,JMG乙酸乙酯提取物对LPS刺激小鼠肺组织p65和i - κ b α磷酸化有抑制作用。结论:JMG乙酸乙酯部位可通过抑制NF-κB p65的磷酸化和减少其核易位,逆转lps诱导的小鼠急性肺出血性坏死和炎症细胞浸润。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
UHPLC-MS analysis for bioactive compounds responsible for the anti-inflammation activities of Jiao Mei Gu on lipopolysaccharide-induced acute lung injury in mice.

Objective: To identify the anti-inflammatory ingredients of a typical Dong herbal medicine Jiao Mei Gu (JMG) (Cayratia albifolia C.L.Li) and reveal the underlying mechanisms.

Methods: For the first time, the chemical constituents in JMG ethyl acetate extract, which showed the highest anti-inflammatory activity, were analyzed by Ultra-performance liquid chromatography-quadrupole-electrostatic field Orbitrap mass spectrometry (UHPLC-Q-Exactive orbitrap MS). The anti-inflammatory activities and the underlying mechanisms of JMG extracts were evaluated in the lipopolysaccharide (LPS)-induced RAW 264.7 cell model and LPS (10 mg/kg) induced acute lung injury model in BALB/c mice.

Key findings: Overall, 65 compounds including lignans, apigenin, quercetin, chrysin, phlorizin, and eriodictyol, etc., were identified in JMG ethyl acetate extract. At 200 mg/kg, JMG ethyl acetate extract reversed the structure change of lung alveoli and inflammatory cell infiltration in LPS-induced acute lung injury model. Compared with the LPS group, the serum levels of IL-1β, IL-6, and TNF-α in the 200 mg/kg JMG-treated group were decreased by 58.6%, 56.5%, and 87.6%, respectively. Western blot results revealed that JMG ethyl acetate extract inhibited LPS stimulated p65 and IκBα phosphorylation in mouse lung.

Conclusion: The present study demonstrated that the ethyl acetate fraction of JMG could reverse LPS-induced acute lung hemorrhagic necrosis and inflammatory cell infiltration in mice by preventing the phosphorylation of NF-κB p65 and reducing its nuclear translocation.

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来源期刊
CiteScore
6.60
自引率
0.00%
发文量
91
审稿时长
3 months
期刊介绍: JPP keeps pace with new research on how drug action may be optimized by new technologies, and attention is given to understanding and improving drug interactions in the body. At the same time, the journal maintains its established and well-respected core strengths in areas such as pharmaceutics and drug delivery, experimental and clinical pharmacology, biopharmaceutics and drug disposition, and drugs from natural sources. JPP publishes at least one special issue on a topical theme each year.
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