Pedunculagin and tellimagrandin-I stimulate inflammation and angiogenesis and upregulate vascular endothelial growth factor and tumor necrosis factor-alpha in vivo

Pedunculagin (PD) and tellimagrandin-I (TL), isolated from Myrciaria cauliflora seeds and Eucaliptus microcorys leaves, respectively, have attracted great attention owing to their relevant biological activities, such as antitumor, antioxidant, and hepatoprotective activities. This study investigated...

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Veröffentlicht in:Microvascular research 2024-01, Vol.151, p.104615-104615, Article 104615
Hauptverfasser: Fernandes, Amanda Silva, de Melo Bisneto, Abel Vieira, Silva, Luana Santos, Bailão, Elisa Flávia Luiz Cardoso, Cardoso, Clever Gomes, Carneiro, Cristiene Costa, da Costa Santos, Suzana, Chen-Chen, Lee
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Sprache:eng
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Zusammenfassung:Pedunculagin (PD) and tellimagrandin-I (TL), isolated from Myrciaria cauliflora seeds and Eucaliptus microcorys leaves, respectively, have attracted great attention owing to their relevant biological activities, such as antitumor, antioxidant, and hepatoprotective activities. This study investigated the angiogenic potential of PD and TL using a chick embryo chorioallantoic membrane (CAM) assay. Using the CAM assay, our results showed that both PD and TL promoted a significant increase in the number and caliber of blood vessels, the thickness of the CAM, and the presence of fibroblasts and inflammatory cells. Moreover, an increase of tumor necrosis factor-α and vascular endothelial growth factor was observed in the CAM treated with PD and TL, indicating the induction of angiogenic factors. Thus, the remarkable profile of PD and TL in inducing angiogenesis opens up new perspectives for their potential utilization in different therapeutic approaches involving neovascularization. •Angiogenic activity of PD and TL were assed in vivo by CAM assay.•PD and TL stimulates inflammation.•PD and TL promoted an increase of new blood vessels.•PD and TL increased the levels of TNF-α and VEGF in CAM.
ISSN:0026-2862
1095-9319
DOI:10.1016/j.mvr.2023.104615