Application of resveratrol in preparing medicines for preventing and treating radiation-induced bone marrow suppression
A technology of bone marrow suppression and resveratrol, applied in the preparation of drugs for the prevention and treatment of radiation-induced bone marrow suppression, the application field of polyphenolic compounds in bone marrow suppression drugs
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Embodiment 1
[0031] Aseptically take the femur of C57BL / 6 mice (Institute of Experimental Animals, Chinese Academy of Medical Sciences), wash the bone marrow with Hanks solution containing 2% fetal bovine serum, separate by density gradient centrifugation, prepare bone marrow mononuclear cell suspension, wash with PBS, and count Adjust the desired cell concentration before use.
[0032] (2) Determination of cell viability
[0033] Add 100 μl of mononuclear cell suspension to the set wells of the 96-well plate, add 100 μl of treatment drugs according to the design, place them in a 37oC carbon dioxide incubator, and cultivate for 18 hours. Take out the culture plate, put it at room temperature, add 20μl of bioluminescent reagent cell-titer, shake and mix well, then transfer to a black assay plate, GloMax TM The luminescence detector uses Promega's own detection program Cell-titer Protocol for detection. The test results automatically generate Excel data.
[0034] (3) Determination of colo...
Embodiment 2
[0043] (1) Immunocytotoxicity to hematopoietic cells
[0044] Isolate mouse bone marrow mononuclear cells, adjust the cell concentration to 2×10 6 / ml. Different concentrations of Res medium were prepared. 100 μl of cell suspension and different concentrations of treatment drugs were added to 96-well culture plates, and after incubation for 18 hours, cell viability was measured by bioluminescence. As a result, it was found that using RPMI-1640 medium (source? The ingredients? Commercially available?) for experiments, Res at a concentration lower than 10 -4 No obvious cytotoxic effect was found at M. See Table 1 and Table 2 for the results. .
[0045]
[0046] (2) Protective effect on radiation injury of hematopoietic immune cells in vitro
[0047] Bone marrow mononuclear cells were isolated, added different concentrations of drugs, incubated for 30 min, and then irradiated. Continue to incubate for 18h after irradiation, and measure cell viability. The results showe...
Embodiment 3
[0067] Example 4
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