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灵芝甾醇通过抑制 LPS 诱导的 RAW264.7 巨噬细胞中 p38MAPK 和 NF-κB 通路发挥抗炎作用。

Anti-inflammatory effects of Ganoderma lucidum sterols via attenuation of the p38 MAPK and NF-κB pathways in LPS-induced RAW 264.7 macrophages.

机构信息

State Key Laboratory of Subtropical Silviculture, Zhejiang Agriculture and Forestry University, Hangzhou, Zhejiang, China.

Westlake University, Hangzhou, Zhejiang, China.

出版信息

Food Chem Toxicol. 2021 Apr;150:112073. doi: 10.1016/j.fct.2021.112073. Epub 2021 Feb 22.

Abstract

Ganoderma lucidum exhibits pronounced anti-inflammatory effects, polysaccharides and triterpenoids are regarded as major constituents displaying the anti-inflammatory activities, whether sterols contribute to this activity remains unclear. Herein Ganoderma lucidum sterols (GLS) were innovatively isolated by a single-step procedure, the profile of GLS was characterized by HPLC-ELSD and shown similar to that of sterols separated by a traditional method, but much higher in content. Furthermore, GLS inhibited inflammation in macrophages by significantly attenuating LPS-induced cell polarization as well as releases and mRNA expressions of pro-inflammatory mediators NO, TNF-α, IL-1β and IL-6. Moreover, the anti-inflammatory activity of GLS was mediated by MAPK and NF-κB pathways, GLS suppressed MAPK pathways by blocking phosphorylation of p38 but not ERK and JNK, which is complementary with inhibitory effects of Ganoderma polysaccharides and triterpenes on JNK and ERK, indicating Ganoderma sterols may exert synergistic anti-inflammatory effect with polysaccharides and triterpenes. GLS also inhibited NF-κB pathways by restraining phosphorylation and degradation of IκB-α and blocking phosphorylation of NF-κB p65. Molecular docking confirmed that sterols of GLS were directly bound to active sites of p38 and p65 to suppress their activation. Therefore, our findings suggest GLS as natural and safe anti-inflammatory agents to prevent and treat inflammatory diseases.

摘要

灵芝具有显著的抗炎作用,多糖和三萜类化合物被认为是主要的抗炎活性成分,而甾醇是否对其具有贡献尚不清楚。本文创新性地采用一步法从灵芝中分离出灵芝甾醇(GLS),通过 HPLC-ELSD 对 GLS 的特征进行了表征,结果表明其与传统方法分离的甾醇相似,但含量更高。此外,GLS 通过显著减弱 LPS 诱导的细胞极化以及促炎介质 NO、TNF-α、IL-1β 和 IL-6 的释放和 mRNA 表达,抑制巨噬细胞炎症。此外,GLS 通过 MAPK 和 NF-κB 途径发挥抗炎活性,通过阻止 p38 的磷酸化而不是 ERK 和 JNK 的磷酸化来抑制 MAPK 途径,这与灵芝多糖和三萜抑制 JNK 和 ERK 的作用互补,表明灵芝甾醇可能与多糖和三萜发挥协同抗炎作用。GLS 还通过抑制 IκB-α的磷酸化和降解以及 NF-κB p65 的磷酸化来抑制 NF-κB 途径。分子对接证实 GLS 的甾醇直接结合到 p38 和 p65 的活性部位以抑制其激活。因此,我们的研究结果表明 GLS 是一种天然、安全的抗炎药物,可用于预防和治疗炎症性疾病。

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