Aerosol Inhalation of Luteolin-7-O-Glucuronide Exerts Anti-Inflammatory Effects by Inhibiting NLRP3 Inflammasome Activation.

IF 4.3 3区 医学 Q2 CHEMISTRY, MEDICINAL Pharmaceuticals Pub Date : 2024-12-21 DOI:10.3390/ph17121731
Jianliang Li, Ling Song, Han Li, Yunhang Gao, Tengfei Chen, Zhongxiu Zhang, Hongping Hon, Zuguang Ye, Guangping Zhang
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Abstract

Background: Luteolin-7-O-glucuronide (L7Gn) is a flavonoid isolated from numerous traditional Chinese herbal medicines that exerts anti-inflammatory effects. Previous research has revealed that aerosol inhalation is the most straightforward way of administration for the delivery of respiratory agents. Thus far, the impact of aerosol inhalation of L7Gn on lung inflammation and the underlying mechanisms remain unknown. Methods: The real-time particle size for L7Gn aerosol inhalation was detected by the Spraytec spray droplet size measurement system, including transmission and size diameters. The acute lung injury (ALI) rat model was induced by aerosol inhalation of LPS to evaluate the protective effect of L7Gn. The inhibitory effect of NLRP3 inflammasome activation assays was conducted in LPS-induced MH-S cells. Elisa, Western blotting, and RT-PCR were utilized to investigate the expression of NLRP3 inflammasome-relevant proteins and genes. Results: In this study, we found that inhalation of L7Gn aerosol significantly reduced pulmonary injury by inhibiting inflammatory infiltration and enhancing lung function. Meanwhile, the NLR family pyrin domain containing 3 (NLRP3) inflammasome was activated dramatically, accompanied by upregulated expression of IL-1β and IL-18, both in the ALI rat model and in LPS-induced MH-S cells. Moreover, L7Gn was found to significantly downregulate the expression of NLRP3, ASC, caspase-1, and cleaved caspase-1, which are critical components of the NLRP3 inflammasome, as well as the expression of IL-1β and IL-18. Conclusions: Based on our findings, L7Gn could exert anti-inflammatory effects by inhibiting NLRP3 inflammasome activation, which may emerge as potential therapeutic agents for the treatment of ALI.

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气溶胶吸入木犀草素-7- o -葡糖苷通过抑制NLRP3炎性小体激活发挥抗炎作用。
背景:木犀草素-7- o -葡糖苷(L7Gn)是从多种中草药中分离出来的具有抗炎作用的类黄酮。先前的研究表明,吸入气溶胶是最直接的给药方式。到目前为止,气溶胶吸入L7Gn对肺部炎症的影响及其潜在机制尚不清楚。方法:采用Spraytec喷雾液滴粒径测量系统,实时检测吸入L7Gn气溶胶的粒径,包括透射率和粒径。采用脂多糖雾化吸入诱导急性肺损伤(ALI)大鼠模型,评价L7Gn的保护作用。在lps诱导的MH-S细胞中进行NLRP3炎性体活化抑制实验。采用Elisa、Western blotting和RT-PCR检测NLRP3炎性小体相关蛋白和基因的表达。结果:本研究中,我们发现吸入L7Gn气雾剂通过抑制炎症浸润,增强肺功能,显著减轻肺损伤。同时,在ALI大鼠模型和lps诱导的MH-S细胞中,NLR家族pyrin结构域3 (NLRP3)炎性小体被显著激活,并伴有IL-1β和IL-18的上调表达。此外,研究发现L7Gn显著下调NLRP3炎性小体的关键成分NLRP3、ASC、caspase-1和cleaved caspase-1的表达,以及IL-1β和IL-18的表达。结论:L7Gn可能通过抑制NLRP3炎性小体的激活而发挥抗炎作用,可能成为治疗ALI的潜在药物。
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来源期刊
Pharmaceuticals
Pharmaceuticals Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
6.10
自引率
4.30%
发文量
1332
审稿时长
6 weeks
期刊介绍: Pharmaceuticals (ISSN 1424-8247) is an international scientific journal of medicinal chemistry and related drug sciences.Our aim is to publish updated reviews as well as research articles with comprehensive theoretical and experimental details. Short communications are also accepted; therefore, there is no restriction on the maximum length of the papers.
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