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Roasted and green coffee extracts show antioxidant and cytotoxic activity in myoblast and endothelial cell lines in a cell specific manner

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Auteur
Priftis A., Panagiotou E.-M., Lakis K., Plika C., Halabalaki M., Ntasi G., Veskoukis A.S., Stagos D., Skaltsounis L.A., Kouretas D.
Date
2018
Language
en
DOI
10.1016/j.fct.2018.02.029
Sujet
carbonyl derivative
reactive oxygen metabolite
thiobarbituric acid reactive substance
antioxidant
chlorogenic acid
glutathione
plant extract
antioxidant activity
Article
cell specificity
cell viability
coffee
controlled study
cytotoxicity
cytotoxicity test
endothelium cell
flow cytometry
human
human cell
myoblast
oxidation reduction state
spectrophotometry
tissue specificity
animal
chemistry
Coffea
coffee
comparative study
cooking
drug effect
endothelium cell
heat
high performance liquid chromatography
mass spectrometry
metabolism
mouse
myoblast
oxidative stress
plant seed
species difference
toxicity
Animals
Antioxidants
Chlorogenic Acid
Chromatography, High Pressure Liquid
Coffea
Coffee
Cooking
Endothelial Cells
Glutathione
Hot Temperature
Humans
Mass Spectrometry
Mice
Myoblasts
Oxidative Stress
Plant Extracts
Seeds
Species Specificity
Elsevier Ltd
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Résumé
Coffee is one of the most highly consumed beverages with potential beneficial health implications, however its molecular mechanism of action has not been completely elucidated yet. To that cause, the polyphenolic composition of different coffee extracts (from Light, Medium and Dark roasts as well as green beans) was examined by UHPLC-HRMS analysis, indicating chlorogenic acids isomers as the main constituents. In the following step, the toxicity of the extracts was tested in myoblasts and endothelial cells and differential toxicity of green and roasted samples was displayed as the myoblasts were more sensitive to green coffee extracts, in contrast to the endothelial cells. Subsequently, biologically relevant, non-cytotoxic extract concentrations were administered to explore their potential effect on cell redox status using flow cytometry and spectrophotometric assays. The results indicated that all coffee extracts improved cell redox status, however differences were observed between the two different cell lines tested, implying that coffee compounds display cell- and tissue-specificity. Glutathione levels were increased in almost all cases up to 70%, while the roasting degree affected the free radical scavenging potential of the extracts and their ability to protect from macromolecular oxidation as exhibited by the differences in ROS, CARB and TBARS levels, especially in the myoblasts. © 2018
URI
http://hdl.handle.net/11615/78365
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19743]
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