Application of mauremys mutica polypeptide mixtures, fatty liver prevention and treatment healthcare product or fatty liver prevention and treatment medicine
A stone money turtle and mixture technology, applied in the direction of medical preparations containing active ingredients, applications, drug combinations, etc., can solve the problems of large toxic and side effects, high cost, and long course of treatment, and achieve good application prospects
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Embodiment 1
[0046] Example 1. Preparation of Polypeptide Mixture
[0047] Mix 10 g of stone turtle meat mince with 80 g of ultrapure water, add neutral protease (25000 U, 37313.43 U / g) and fully react for 10 hours under the conditions of a temperature of 45° C. and a pH of 7.5 to obtain a reaction liquid.
[0048] The reaction solution was enzymatically inactivated at 85°C for 10 minutes, centrifuged at 8000r / min for 30 minutes, the precipitate was removed and the supernatant was preserved, and the supernatant was freeze-dried to obtain the crude product, which is the Polypeptide Mixture.
[0049] Dilute the obtained Glycine max polypeptide (GDP) mixture to an original concentration of 1 g / mL, and store it at 4°C for later use.
Embodiment 2
[0050] Example 2. Determination of the improvement of oleic acid, glucose and alcohol-induced HepG2 fatty liver by the Polypeptide Mixture
[0051] 1. Determination of Toxicity of Polypeptide Mixture of Pterocephalidae to HepG2
[0052] Take HepG2 cells in logarithmic growth phase (Shanghai Cell Bank, ATCC) and adjust the cell density to 2×l0 5 cells / mL, add the adjusted concentration of the cell suspension to a 96-well (100μL / well) culture plate, place it in the incubator for 24 hours, and then add a suspension containing different concentrations of Shimochi polypeptide mixture (0,50μg / mL, 100μg / mL, 150μg / mL, 200μg / mL, 250μg / mL, 300μg / mL), and set up a control group at the same time, and set up 3 multiple wells for each group. After culturing for 24h, add 20μL MTT reagent to each well ( 5mg / mL), 37℃, 5% CO 2 Continue to incubate for 4 hours in the incubator, aspirate the culture supernatant in the wells, add 150μL DMSO to each well, shake for 10 minutes, measure the absorbance va...
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