Identification, Characterization and Anti-inflammatory Activity of a New Flavonoid From Hibiscus mutabilis L.

IF 2.3 4区 医学 Q3 PHARMACOLOGY & PHARMACY Dose-Response Pub Date : 2024-12-20 eCollection Date: 2024-10-01 DOI:10.1177/15593258241290130
Pan Hu, Lei Ye, Yuanxiang Gong, Xin Yan, Ping Huang, Xiaoqing Shi, Xi Wang
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Abstract

Hibiscus mutabilis L (Malvaceae) was a traditional Chinese medicine with significant anti-inflammatory activity. We isolated 3 compounds from the flowers of H mutabilis L , including a new flavonoid, (1″R)-8-(1-(3,4-dihydroxyphenyl)ethyl)-3,3',5,7-tetrahydroxy-4'-methoxyl flavone (1), and 2 known flavonoids (2-3). The structures of these compounds were elucidated by various spectroscopic methods. In addition, we evaluated the anti-inflammatory effect of compound 1. The bioactivity assay showed that 1 significantly inhibit the excessive production of IL-6, TNF-α and NO in LPS-induced RAW264.7 macrophages. Western blot analysis demonstrated that 1 inhibit the expressions of COX-2 and iNOS protein in the macrophages induced by LPS in a concentration-dependent manner. In addition, 1 also significantly suppress the expression of the key proteins P65 and p-P65 in the NF-κB signaling pathway. Our results revealed that 1 exert potential anti-inflammatory activity through inhibiting the activation of NF-κB signaling pathway.

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一种新型木槿黄酮类化合物的鉴定、表征及抗炎活性研究。
木槿(malvacae)是一种具有显著抗炎活性的中药。我们从变异黄酮(H mutabilis L)花中分离到3个化合物,包括一个新的类黄酮(1″R)-8-(1-(3,4-二羟基苯基)乙基)-3,3',5,7-四羟基-4'-甲氧基黄酮(1)和2个已知的类黄酮(2-3)。这些化合物的结构用各种光谱方法进行了分析。此外,我们对化合物1的抗炎作用进行了评价。生物活性测定结果显示,1能显著抑制lps诱导的RAW264.7巨噬细胞过量产生IL-6、TNF-α和NO。Western blot分析显示,1对LPS诱导的巨噬细胞中COX-2和iNOS蛋白的表达呈浓度依赖性。此外,1还显著抑制NF-κB信号通路中关键蛋白P65和p-P65的表达。我们的研究结果表明,1通过抑制NF-κB信号通路的激活发挥潜在的抗炎活性。
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来源期刊
Dose-Response
Dose-Response PHARMACOLOGY & PHARMACY-RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
CiteScore
4.90
自引率
4.00%
发文量
140
审稿时长
>12 weeks
期刊介绍: Dose-Response is an open access peer-reviewed online journal publishing original findings and commentaries on the occurrence of dose-response relationships across a broad range of disciplines. Particular interest focuses on experimental evidence providing mechanistic understanding of nonlinear dose-response relationships.
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