New application of luteolin
A technology for the application of luteolin, which is applied in the new application field of luteolin, and can solve the problems such as the antiviral effect of luteolin that have not been reported
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Embodiment 1
[0022] Example 1: Cytotoxicity of luteolin to cells and inhibition of cytopathic effects caused by Enterovirus 71 and Coxsackievirus A16
[0023] Human rhabdomyosarcoma cells in the logarithmic growth phase (RD cells, purchased from ATCC, accession number: #CCL-136) and RD cells stably expressing the EV71 / CA16 receptor hSCARB2 gene (NCBI accession number: NM_005506.3) RDS cells were obtained from the National Engineering Laboratory of AIDS Vaccine, Jilin University. For the construction method, see Lietal. 4 pcs / hole and 6×10 4 The concentration of cells / well was inserted into a 96-well culture plate and cultured for 24 hours. Both RD cells and RDS cells were incubated at 37 °C and 5% CO 2 The medium used for culturing RD cells was DMEM medium supplemented with 10% fetal bovine serum (abbreviated as 10% FBS-DMEM, both FBS and DMEM were purchased from Sigma), and the medium used for cultivating RDS cells was containing 0.5 μg / ml puromycin (purchased from Clontech) in 10% FBS...
Embodiment 2
[0039] Example 2: Inhibitory effect of luteolin on plaque formation caused by EV71 and CA16
[0040] Take the RDS cells in the logarithmic growth phase, and use 6×10 5 The concentration of each well was inserted into a 12-well culture plate and cultured for 24 hours.
[0041] Aspirate the medium in each well, add 300 μL of 2% FBS-DMEM cell culture solution containing different concentrations of luteolin, so that the final concentration of luteolin in the well is 50 μM, 25 μM, 12.5 μM, 6.25 μM, each concentration is set to 3 Multiple wells; add 300 μ LEV71 or CA16 (100 PFU / hole) virus to each well while adding medicine to infect; and set only adding 2% FBS-DMEM cell culture medium cell control and only adding EV71 or CA16 to infect the virus control; After continuing to culture the cells for 1 hour, suck off the culture supernatant and rinse the cells twice with sterile PBS, add 1% agar 2% FBS-DMEM medium containing corresponding concentrations of luteolin to the drug-dosed gr...
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