Use of lysophosphatidic acid, lysophosphatidic acid receptor 3, and lysophosphatidic acid receptor 3 agonists
A technology of lysophosphatidic acid and receptors, applied in the field of biomedicine
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Embodiment 1
[0040] Effects of LPA3 overexpression on cardiac function and infarct size after myocardial infarction in mice
[0041] (1) Establishment of mouse myocardial infarction model
[0042]After weighing and recording the body weight of the mice, they were anesthetized by intraperitoneal injection of tribromoethanol solution at a concentration of 400 mg / kg (about 0.2 mL for mice with about 25 ng);
[0043] Disinfect the left chest of the mouse with 75% alcohol, use depilatory cream to remove the hair near the surgical field of view; carry out tracheal intubation, and connect the ventilator;
[0044] Cut the skin on the outside of the left chest along the parallel direction of the left ribs, bluntly separate the muscles of each layer along the direction of the muscle shape to expose the ribs, and use a spreader to stretch the muscles so that the rib layer is exposed in the center of the field of vision; in the 3rd-4th intercostal space Use fine straight forceps to separate the muscl...
Embodiment 2
[0057] Effect of overexpression of LPA3 on the proliferation of cardiomyocytes after myocardial infarction in mice
[0058] (1) Experimental grouping and processing
[0059] With embodiment 1.
[0060] (2) Experimental method
[0061] Using a mouse model of myocardial infarction, LPA3 overexpression and control viruses were injected into the infarction area at the same time, and heart samples were collected 8 weeks after myocardial infarction, and the myocardial marker α-s-actin and proliferation marker Ki67 were co-stained by immunofluorescence. pH3. The specific method is to dewax the prepared paraffin slices and carry out antigen retrieval. After washing with phosphate buffer, block with goat serum for 1 hour, and then add an appropriate concentration of primary antibody (anti-α-s-actin, Ki67 or pH3)4 Incubate overnight at ℃, wash with phosphate buffer, add appropriate concentrations of secondary antibodies with different fluorescence and incubate at 37°C in the dark for...
Embodiment 3
[0065] Effect of overexpression of LPA3 on myocardial cell apoptosis after myocardial infarction in mice
[0066] (1) Experimental grouping and processing
[0067] With embodiment 1.
[0068] (2) Experimental method
[0069] Using a mouse model of myocardial infarction, LPA3 overexpression and control viruses were injected into the infarct area at the same time as the infarction, and heart samples were collected 8 weeks after myocardial infarction, and the apoptosis of myocardial cells in the peri-infarction area and infarct distal end was detected by TUNEL experiment. The specific method In order to dewax the prepared paraffin slices, pretreat with proteinase K to break the cell membrane, then block with goat serum for 1 hour, add an appropriate concentration of cTNT antibody and incubate overnight at 4°C, wash with phosphate buffer and add an appropriate concentration of fluorescence The secondary antibody was incubated at 37°C in the dark for 1 hour, washed with phosphate...
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