Application of scutellarin in preparation of medicine for preventing and treating atherosclerosis
A technology for atherosclerosis and scutellarin, which is applied in the fields of biomedicine and medicine, can solve the problem that the mechanism of scutellarin against AS is not clear, and achieve the effect of lowering blood lipid levels
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Embodiment 1
[0042] Example 1 The effect of scutellarin (Scu) on AS by regulating the PERK-Nrf2 / ATF4-CHOP pathway
[0043] 1. Animal AS model establishment and processing
[0044] Forty healthy male SD rats were randomly divided into 4 groups, with 10 rats in each group. They were respectively set as: (A) blank control group; (B) model group; (C) scutellarin low-dose group; (D) scutellarin high-dose group. The feeding and administration methods of each group are shown in Table 1. Show. SD rats were administered daily and weighed once a week during feeding, and model establishment was terminated after continuous feeding for 12w. After fasting for 12 hours, SD rats were anesthetized with 10% chloral hydrate, and the abdominal aortic blood was taken out into EP tubes, and after standing for 4 hours, centrifuged at 3000 rpm at 4°C for 10 minutes, the supernatant was taken and stored in a -80°C refrigerator .
[0045] Table 1 Each group of animal feeding and administration methods
[0046]...
Embodiment 2
[0091] Example 2 Protective effect of scutellarin on HAECs cell damage induced by 2,2-azobis(2-methylpropylimidium) dihydrochloride (AAPH)
[0092] 1. Culture of human aortic endothelial cells (HAECs)
[0093] Take out the cell cryopreservation tube and quickly dissolve it in a 37°C water bath. Add an appropriate amount of cell culture medium to the centrifuge tube in advance, transfer the liquid in the cryopreservation tube into the prepared centrifuge tube in a sterile ultra-clean bench, blow and beat evenly, and centrifuge at 1000g for 5min. Keep only the precipitate, add 2mL of cell culture medium to pipette the precipitate into a cell suspension. Transfer the cell suspension into a culture flask, and add 1 mL of cell culture medium. Place at 37°C with 5% CO 2 Cultured in an incubator, and the medium was changed the next day.
[0094] When the cells basically covered the bottom of the bottle, they were digested and subcultured with 0.25% trypsin (containing 0.02% EDTA)...
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