The MTT (Sigma-Aldrich, St. Louis, MO, USA) cell viability assay was used to determine the viability of cells following treatment with licorice TE- and compounds-only and the pre-treatment of cells with licorice TE and/or compounds and MPP+. Cells were seeded in 96-well plates and treated as stated above, after which the MTT assay was performed. After treatment, 10 or 20 µL (depending on well volume) of the 5 mg/mL MTT solution in phosphate-buffered saline (PBS) (Lonza Group Ltd., Verviers, Belgium) was added to each well and left to incubate in the dark at 37 °C for 4 h. After incubation, the medium containing the MTT dye was discarded, and the MTT formazan was solubilized with 100 μL of DMSO for an absorbance reading using a microplate reader (BMG Labtech Omega® POLARStar, Offenburg, Germany) at a wavelength of 570 nm. Cell viability was calculated and expressed as a percentage of control.
Do you have any questions about this protocol?
Post your question to gather feedback from the community. We will also invite the authors of this article to respond.