Application of fisetin in preparation of medicine for preventing and treating uric acid nephropathy
A technology for uric acid nephropathy and fisetin, which is applied in the field of medicine and can solve the problems that patients are not easily tolerated, and the clinical application of allopurinol is limited.
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Embodiment 1
[0031] Example 1 The effect of fisetin on preventing uric acid nephropathy
[0032] Experimental animals: SPF grade male C57BL / 6J mice. At least 1 week before the experiment, the rats were fed with a standardized experimental diet in a constant temperature environment, with unlimited drinking water.
[0033] Grouping of animals: Divide 30 mice into 5 groups: ① normal control group 6; ② uric acid nephropathy model group 6; ③ fisetin treatment group (50mg / kg / d and 100mg / kg / d) 6 ④ positive control allopurinol treatment group (10mg / kg / d) 6.
[0034] Modeling method: According to the weight of the mouse, the proportion of adenine 160mg / kg and potassium oxonate 2500mg / kg was mixed with distilled water to make a suspension with a final concentration of 80g / L, and the next day was administered orally in the morning and evening. For 28 consecutive days, an animal model of hyperuricemia renal damage was established. After 28 days, the mice were sacrificed, blood was collected from th...
Embodiment 2
[0046] Embodiment 2 The effect of fisetin in treating uric acid nephropathy
[0047] Experimental animals: SPF grade male C57BL / 6J mice. At least 1 week before the experiment, the rats were fed with a standardized experimental diet in a constant temperature environment, with unlimited drinking water.
[0048] Grouping of animals: Divide 24 mice into 4 groups: ① normal control group 6; ② uric acid nephropathy model group 6; ③ fisetin treatment group (100mg / kg / d) 6; ④ allopurinol treatment Group (10mg / kg / d) 6. Modeling method: According to the weight of the mouse, the proportion of adenine 160mg / kg and potassium oxonate 2500mg / kg was mixed with distilled water to make a suspension with a final concentration of 80g / L, and the next day was administered orally in the morning and evening. For 14 consecutive days, an animal model of hyperuricemia renal damage was established. After 28 days, the mice were sacrificed, blood was collected from the orbital venous plexus, and kidney ti...
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