4.7 Article

C-geranylated flavonoids from Paulownia tomentosa Steud. fruit as potential anti-inflammatory agents

Journal

JOURNAL OF ETHNOPHARMACOLOGY
Volume 296, Issue -, Pages -

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.jep.2022.115509

Keywords

Anti-inflammatory; Geranylated flavonoids; NF -KB; Paulownia tomentosa; THP-1-XBlue TM-MD2-CD14

Funding

  1. Czech Sciences Foundation [AT-CZ 21-38204L]
  2. Masaryk University, Grant Agency of Masaryk University [MUNI/C/0032/2021]
  3. Masaryk University [MUNI/A/1688/2020, MUNI/A/1654/2020]
  4. Research infrastructure METROFOOD-CZ (Ministry of Education, Youth and Sports of the Czech Republic) [LM2018100]

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Paulownia tomentosa Steud., a traditional Chinese medicinal plant, is rich in phenolic compounds and has potential anti-inflammatory activities. This study isolated several flavonoids from the fruit of P. tomentosa and evaluated their cytotoxicity and anti-inflammatory effects. The results showed that these flavonoids reduced the activation of NF-KB/AP-1, indicating their potential as a source for new anti-inflammatory medications.
Ethnopharmacological relevance: Paulownia tomentosa Steud., a traditional Chinese medicinal plant, was used for many centuries in Chinese herbal medicine as a component of remedies for many illnesses, including inflammatory diseases. It is a rich source of phenolic compounds, mainly geranylated flavonoids, which are currently studied for their promising biological activities. Aim of the study: The study aimed to isolate minor geranylated flavanones and flavones from P. tomentosa fruit and evaluate their cytotoxicity and possible anti-inflammatory effects in a cell-based model of inflammation. Materials and methods: Chromatographic separation of chloroform portion of the ethanolic extract of P. tomentosa fruit led to the isolation of twenty-seven flavonoids (1-27), twenty-six of them geranylated with different modifications and one non-geranylated flavanone, and two phenolic compounds. Compounds were identified using UV, IR, HRMS, NMR, and CD spectroscopy. Ten of these compounds (7-10, 12, 21, 22, 24, 25, and 27) were determined to be new flavonoid derivatives obtained from a natural source for the first time. Selected compounds were analyzed for cytotoxicity and anti-inflammatory potential to affect the activation of nuclear factor KB/activator protein 1 (NF-KB/AP-1) after lipopolysaccharide (LPS) stimulation. Results: All the test compounds (1-21 and 23-26) reduced the activation of NF-KB/AP-1 24 h after the addition of LPS. Eight compounds (5, 14-18, 21, and 26) were more active than prednisone, a widely used antiinflammatory drug. However, this effect was not seen significantly on the level of TNF-alpha and IL-1fl, which can be explained by the plurality of possible outcomes of activation of the NF-KB pathway in cells. Conclusions: Results of the presented study confirmed that constituents from traditional Chinese medicinal plant P. tomentosa Steud. have promising anti-inflammatory activities and can serve as a potential source of inspiration for new anti-inflammatory medications.

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