Short peptide, and applications of compositions thereof in treatment/prevention of diabetes and related diseases thereof
A composition and technology for diabetes, applied in the field of peptides, can solve the problems of patients' health side effects, inability to effectively treat or improve diabetes and its complications, etc.
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Embodiment 1
[0055] Example 1: Preparation of short peptides
[0056] Prepare the disclosed IF and DF peptides of the present invention by chemical synthesis, and confirm the purity of the IF and DF peptides by HPLC, the results are as follows figure 1 and figure 2 As shown, it was shown that the peptides prepared by the chemical synthesis method had high purity.
Embodiment 2
[0057] Example 2: Cell Culture
[0058] H9c2 cells (ATCC, CRL-1446) were purchased from the American Type Culture Collection (Rockville, MD). H9c2 cells were cultured in DMEM medium (DMEM) supplemented with 2 mM glutamine, 10% bovine serum (Cosmic Calf Serum), 100 U / mL penicillin and streptomycin, and 1 mM sodium pyruvate under the following conditions: 37°C, Moist air (5% carbon dioxide).
Embodiment 3
[0059] Example 3: Cell Experiment
[0060] H9c2 cells were divided into several groups, including:
[0061] The control group was cultured with normal glucose (22mM) medium;
[0062] High glucose group: cultured in medium containing high glucose (33mM);
[0063] Low-dose IF peptide group: cultured in medium containing high glucose (33mM) and 5μg of IF peptide;
[0064] High-dose IF peptide group: cultured in medium containing high glucose (33mM) and 10μg of IF peptide;
[0065] Low-dose DF peptide group: cultured in medium containing high glucose (33mM) and 5μg of IF peptide;
[0066] High-dose DF peptide group: cultured in medium containing high glucose (33 mM) and 10 μg of IF peptide.
[0067] Cells in each group were cultured in their conditions for 24 hours before subsequent analysis.
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