Bioactivites of two common polyphenolic compounds: Verbascoside and catechin

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Abstract

Context: Natural products can present remarkable biological and pharmacological activities. In traditional medicine, plants have been used historically in treating cancer, infections, and other inflammatory conditions. Objective: Verbascoside and catechin are widespread polyphenolic plant compounds that could play a role in the anti-inflammatory and health-promoting effects of plants and plant extracts. Materials and methods: This study compares the potential cytotoxic effects of polyphenols verbascoside and catechin (6.25-200 μM) on human peripheral blood mononuclear cells (PBMC) for 48 h and myelomonocytic THP-1 and THP-1 Blue cells for 24 h. The effects of the compounds on immune activation markers such as indoleamine 2,3-dioxygenase (IDO) activity as well as on neopterin formation and nuclear factor-κB (NF-κB) activation were investigated. Cytotoxicity of the compounds was tested using Cell-Titer Blue assay. Results: Verbascoside exhibited significant suppressive effects in mitogen-stimulated PBMC on tryptophan breakdown (>50 μM; IC50 value: 58.6 μM) and the production of neopterin (>6.25 μM; IC50 value: 217 μM). These effects correlated with a decline in cell viability, while THP-1 Blue cells were less sensitive. NF-B activity was slightly enhanced at lower concentrations (<50 μM verbascoside) in stimulated cells and at the highest concentration used in unstimulated cells. Catechin had no relevant effects on cell viability and on the tested inflammation markers, except NF-κB activation in THP-1 Blue cells. Discussion and conclusion: The results obtained show that verbascoside and catechin represent effective compounds which interfere with immunobiochemical pathways that are highly relevant for immunosurveillance and competing virus infections.

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Sipahi, H., Gostner, J. M., Becker, K., Charehsaz, M., Kirmizibekmez, H., Schennach, H., … Fuchs, D. (2016). Bioactivites of two common polyphenolic compounds: Verbascoside and catechin. Pharmaceutical Biology, 54(4), 712–719. https://doi.org/10.3109/13880209.2015.1072830

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