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Anti-inflammatory activities of several diterpenoids isolated from Hemionitis albofusca.
Pei, Xiaoxiao; Lou, Yuxia; Ren, Qianqian; Liu, Yan; Dai, Xiling; Ye, Mingfu; Huang, Guozheng; Cao, Jianguo.
Afiliação
  • Pei X; College of Life Science, Shanghai Normal University, Shanghai, 201418, People's Republic of China.
  • Lou Y; College of Life Science, Shanghai Normal University, Shanghai, 201418, People's Republic of China.
  • Ren Q; College of Life Science, Shanghai Normal University, Shanghai, 201418, People's Republic of China.
  • Liu Y; Maanshan Institute for Food and Drug Control and Adverse Drug Reaction, Ma'anshan, 243000, People's Republic of China.
  • Dai X; College of Life Science, Shanghai Normal University, Shanghai, 201418, People's Republic of China.
  • Ye M; College of Chemistry and Chemical Engineering, Anhui University of Technology, Ma'anshan, 243002, People's Republic of China.
  • Huang G; College of Life Science, Shanghai Normal University, Shanghai, 201418, People's Republic of China. guozheng.huang@ahut.edu.cn.
  • Cao J; College of Chemistry and Chemical Engineering, Anhui University of Technology, Ma'anshan, 243002, People's Republic of China. guozheng.huang@ahut.edu.cn.
Naunyn Schmiedebergs Arch Pharmacol ; 397(1): 437-449, 2024 01.
Article em En | MEDLINE | ID: mdl-37462718
Hemionitis albofusca (Baker) Christenh is a plant that grows in various regions of China. Although it is not recognized as a traditional medicine, it is often mistakenly labelled and used as Aleuritopteris argentea (S. G. Gmél.) Fée to alleviate menstruation-related issues. Recently, several diterpenoids such as ent-16-oxo-17-norkauran-19-oic acid (Compound A), 14-oxy-7ß,20-dihydroxycyath-12,18-diene (Compound B), ent-8(14),15-pimaradiene-2ß,19-diol (Compound C), ent-kaurane-16-ene-2ß,18α-diol (Compound D), ent-kaurane-2ß,16α,18α-triol (Compound E), and onychiol B have been extracted from H. albofusca. In this study, we investigated the anti-inflammatory activity of these diterpenes. We confirmed that compounds A ~ D suppressed the amount of cellular NO production by inhibiting the expression and transcription of iNOS protein. They also significantly inhibited the expression and transcription of inflammatory factors TNF-α and IL-6. Additionally, Compounds A and C suppressed the activation of the NF-κB signaling pathway and inhibited the phosphorylation level of p38, ultimately down-regulating inflammation. Compound B suppressed the activation of the NF-κB signaling pathway, while Compound D inhibited the phosphorylation level of p38 and down-regulated the activation of the p38 MAPK signaling pathway. In a word, our investigation supports the potential application of natural diterpenes as lead compounds for developing anti-inflammatory agents.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diterpenos do Tipo Caurano / Diterpenos Idioma: En Revista: Naunyn Schmiedebergs Arch Pharmacol Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diterpenos do Tipo Caurano / Diterpenos Idioma: En Revista: Naunyn Schmiedebergs Arch Pharmacol Ano de publicação: 2024 Tipo de documento: Article