Active oligopeptide GRGDS and application thereof in preparation of drug for preventing and treating ischemic cerebrovascular diseases
A cerebrovascular disease and ischemic technology, which is applied in the field of active short peptides, namely GRGDS, for the preparation of anti-ischemic cerebrovascular disease products, and achieves the effect of good application prospects.
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Embodiment 1
[0024] Embodiment 1: the preparation method of active short peptide GRGDS
[0025] Amino acid sequence: Gly-Arg-Gly-Asp-Ser (GRGDS)
[0026] The above polypeptide molecules were synthesized by China Peptide Biochemical Co., Ltd., with a purity of more than 98%.
Embodiment 2
[0027] Embodiment 2: GRGDS is used for the animal experiment of treating ischemic cerebrovascular disease
[0028] Rat ischemia-reperfusion model is a commonly used animal experimental model to verify that drugs can prevent and treat ischemic cerebrovascular disease (Xu Shuyun, Bian Rulian, Chen Xiu. Pharmacological Experimental Methodology (Third Edition). People's Medical Publishing House, 2002: 1061- 1062.), so it was used to verify the protective effect of the active short peptide GRGDS on experimental cerebral ischemia in rats.
[0029] 1. Animals
[0030] Healthy male SD rats, weighing 200-250 g, were reared in groups of 6 rats / cage, and divided into 10 groups in total. Purchased from Shanghai Slack Experimental Animal Co., Ltd., quality certificate number (animal certificate number: SCXK (Shanghai) 2007-0005). Raised in a clean animal room.
[0031] 2. Drugs
[0032] Group the experimental rats into groups:
[0033] Sham operation group: given the same amount of no...
Embodiment 3
[0046] Embodiment 3: GRGDS is used in the cell experiment of treating ischemic cerebrovascular disease
[0047] 1. Experimental method
[0048] Select PC12 cells (rat nerve cells) in good growth state and spread them in 96-well plates. After culturing in a constant temperature incubator at 37°C for 16 hours, the normal group continued normal culture with new high-sugar DMEM medium; the OGD group was replaced with sugar-free DMEM medium, and cultured in hypoxia for 6 hours; the GRGDS group was added with 0.01ug / mL GRDGS was cultured in sugar-free DMEM medium for 6 hours in hypoxia. After the end of hypoxia, operate according to the instructions in the apoptosis kit, and then use flow cytometry to detect the apoptosis of cells in each group.
[0049] All data are represented by ± s, and statistical analysis was performed using t test.
[0050] 2. Experimental results
[0051] see attached image 3 , the total apoptosis rate in the normal group was (2.26±0.61)%; the total cell...
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