Application of polypeptide to preparation of medicines for preventing or treating metabolic syndromes
A technology for drugs and compositions, applied in metabolic diseases, drug combinations, pharmaceutical formulations, etc., can solve problems such as unsatisfactory curative effects, and achieve the effects of improving abnormal glucose and lipid metabolism, reducing the weight of adipose tissue, and reducing blood sugar
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Embodiment 1
[0037] Embodiment 1. Preparation of polypeptide
[0038] Peptide Glu 1 -Thr 2 -Pro 3 -Asp 4 -Cys 5 -Phe 6 -Trp 7 -Lys 8 -Tyr 9 -Cys 10 -Val 11 (disulfide bond Cys 5 -Cys 10 ) is chemically synthesized (specifically by solid-phase synthesis), and the HPLC purity is greater than 95%. The peptide powder was dissolved in physiological saline to prepare a solution of 1000 μg / ml, and after aliquoting, it was frozen and stored at -80°C for later use. Dilute with normal saline to the corresponding concentration when used.
Embodiment 2
[0039] Embodiment 2. Effect of active polypeptide on normal animals
[0040] 10 C57BL / J male mice (Beijing Huafukang Biotechnology Co., Ltd.), weighing 17-20 g, were fed with complete nutritional feed, without restriction of water. Urotensin 27.8 μg / kg (20 nmol / kg) was administered, and body weight was monitored weekly. Once a day for 14 days. Animals were fasted overnight before glucose and insulin tolerance assays. 2g / kg or 0.75U / kg insulin were administered after measuring basal blood glucose. Blood glucose levels were measured at 15, 30, 60, and 120 minute time points. After the experiment, the visceral index and serum markers were measured.
Embodiment 3
[0041] Example 3. Effect of Active Polypeptides on High Fat Feed Induced Metabolic Syndrome / Type 2 Diabetes / Obesity Animals
[0042] Male C57BL / J mice, weighing 17-20 g, were fed with high-fat diet and were not limited to water. C57BL / J mice of the same age were used as a normal control group, weighing 17-20 g, fed with complete nutrition feed, without water restriction. Monitor body weight weekly. After the high-fat-fed mice were 10 g heavier than the normal control, the mice in the obese group were randomly divided into two groups: the high-fat control group and the Urotensin 2 administration group. The urotensin administration group was intraperitoneally injected with polypeptide 27.8 μg / kg (20 nmol / kg), and the normal and high-fat control groups were intraperitoneally injected with the same volume of normal saline. Continuous administration for 3 weeks. Blood sugar and body weight were measured weekly. Animal deaths were recorded. After the experiment, the visceral in...
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