2017
DOI: 10.4490/algae.2017.32.11.29
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Protective effect of gallic acid derivatives from the freshwater green alga Spirogyra sp. against ultraviolet B-induced apoptosis through reactive oxygen species clearance in human keratinocytes and zebrafish

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Cited by 37 publications
(32 citation statements)
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References 35 publications
(32 reference statements)
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“…The FD-containing media were carefully removed and washed three times, followed by adding new media. MTT and DCFH-DA assays were conducted to measure the cell viability and intracellular ROS generation, respectively [16].…”
Section: Cell Viability and Ros Productionmentioning
confidence: 99%
“…The FD-containing media were carefully removed and washed three times, followed by adding new media. MTT and DCFH-DA assays were conducted to measure the cell viability and intracellular ROS generation, respectively [16].…”
Section: Cell Viability and Ros Productionmentioning
confidence: 99%
“…UVB irradiation was imposed using a UVB meter (UV Lamp, VL-6LM, Vilber Lourmat, France) with a fluorescent bulb emitting at 280-320 nm with a peak at 313 nm. HaCaT cells were irradiated at a dose of 30 mJ/cm 2 of UVB in PBS (Wang et al 2017). After UVB irradiation, cells were incubated with serum-free DMEM media until analysis.…”
Section: Cell Culture and Uvb Irradiationmentioning
confidence: 99%
“…To determine the effect of HFPS on UVB-irradiated HaCaT cells, intracellular ROS levels, cell viability, and apoptosis body formation were measured. The intracellular ROS levels of UVB-irradiated HaCaT cells were determined using a DCF-DA assay and cell viability was measured by an MTT assay following the protocols described in a previous study (Wang et al 2017). Apoptosis body formation in UVBirradiated HaCaT cells was determined by Hoechst 33342 nuclear staining according to the method described by Wijesinghe et al (Wijesinghe et al 2013).…”
Section: Measurement Of the Effect Of Hfps On Uvb-irradiated Hacat Cellsmentioning
confidence: 99%
“…Cell viability was quantified by a colorimetric MTT assay (Wang et al 2017;Wang et al 2018). Briefly, B16F10 cells were seeded in a 96-well plate and incubated for 24 h. The cells were treated with different concentrations of test samples and incubated for 72 h. MTT solution (50 μL, 2 mg/mL) was added to each well and incubated for 3 h. The supernatant was aspirated, 150 μL of DMSO was added to each well, and the absorbance was measured at 540 nm using a microplate reader.…”
Section: Cell Viability Assaymentioning
confidence: 99%