Application of total paeony glycosides to preparation of medicine for preventing or treating microwave radiation induced nerve cell injury, pharmaceutical composition and food
A technology of nerve cell damage and total glucosides of paeony, which is applied in the field of medicine, can solve the problems that research and development still need to be strengthened, and achieve the effect of reducing nerve cell damage, reducing content, and repairing nerve cells
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0062] Example 1 Effect of total glucosides of paeony on changes in ROS content in H9c2 nerve cells induced by microwave radiation
[0063] 1. Culture induced PC12 cells
[0064] Take out the PC12 cell line with the characteristics of neurons and neurosecretory cells from liquid nitrogen, put it into water at 37 degrees Celsius, suck it into a centrifuge tube after melting, and then add 1.5 ml of 10% fetal bovine serum, 5% horse serum, and 100 units of penicillin / DMEM culture medium (dubecco'sminimallessentialmedium, DMEM) of 100 micrograms / ml of streptomycin, centrifuged at 1000 rpm for 10 minutes, discarded the supernatant, added 4 ml of the above-mentioned medium, pipet evenly, and sucked it into the culture bottle. Change medium every other day, 37°C, 5% CO 2 Cultivation and passage under conditions; after the above-mentioned cultured cell line was passed for 3 generations, it was induced to differentiate into neuron-like cells by using DMEM medium with 5 ng / ml NGF and 1...
Embodiment 2
[0084] Example 2 Effect of total glucosides of paeony on changes in ROS content in PC12 cells induced by microwave radiation
[0085] 1. Culture and induction of PC12 cells
[0086] Take out the PC12 cell line with the characteristics of neurons and neurosecretory cells from liquid nitrogen, put it into water at 37 degrees Celsius, suck it into a centrifuge tube after melting, and then add 1.5 ml of 10% fetal bovine serum, 5% horse serum, and 100 units of penicillin / DMEM culture medium (dubecco'sminimallessentialmedium, DMEM) of 100 micrograms / ml of streptomycin, centrifuged at 1000 rpm for 10 minutes, discarded the supernatant, added 4 ml of the above-mentioned medium, pipet evenly, and sucked it into the culture bottle. Change medium every other day, 37°C, 5% CO 2 Cultivation and passage under conditions; after the above-mentioned cultured cell line was passed for 3 generations, it was induced to differentiate into neuron-like cells by using DMEM medium with 5 ng / ml NGF an...
Embodiment 3
[0098] Example 3 Effect of total glucosides of paeony on changes in MDA content in PC12 cells induced by microwave radiation
[0099] 1. Culture and induction of PC12 cells
[0100] Take out the PC12 cell line with the characteristics of neurons and neurosecretory cells from liquid nitrogen, put it into water at 37 degrees Celsius, suck it into a centrifuge tube after melting, and then add 1.5 ml of 10% fetal bovine serum, 5% horse serum, and 100 units of penicillin / DMEM culture medium (dubecco'sminimallessentialmedium, DMEM) of 100 micrograms / ml of streptomycin, centrifuged at 1000 rpm for 10 minutes, discarded the supernatant, added 4 ml of the above-mentioned medium, pipet evenly, and sucked it into the culture bottle. Change medium every other day, 37°C, 5% CO 2 Cultivation and passage under conditions; after the above-mentioned cultured cell line was passed for 3 generations, it was induced to differentiate into neuron-like cells by using DMEM medium with 5 ng / ml NGF an...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 