Application of protective medicine for ischemia reperfusion injury prepared by mitochondrial complex I reversibility inhibitor and active oxygen scavenger
A technology of mitochondrial complex and active oxygen scavenger, which is applied in the field of medicine to achieve the effect of improving the therapeutic effect and improving the therapeutic effect
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Embodiment 1
[0030] Example 1: Therapeutic effect on myocardial ischemia-reperfusion
[0031] 1. Experimental materials
[0032] H9c2 cells, N2a cells, HK-2 cells: purchased from ATCC Company and preserved by our laboratory. DMEM high-glucose medium, fetal bovine serum, 0.25% trypsin, 100× penicillin and streptomycin, CalceinAM (Thermo Fisher, USA), PBS (Beijing Boaosen Biotechnology Co., Ltd.), CoCl 2 , hydrogen peroxide (US Sigma Company), PhosSTOP, completeULTRATablets, Mini EASYpack (Roche Company), CCK8, Fluo-4AM, Rhod-2AM (Shanghai Dongren Chemical Technology Co., Ltd.), RIPA lysate, LY294002 (Shanghai Biyuntian Bio Technology Co., Ltd.), AKT, p-AKT, p-GSK3, β-actin (Cell Signaling Technology, USA). Ultra-clean bench (Thermo Company, USA, ThermoScientific 1300A2 type), multifunctional microplate reader FLUOstar Omega (Germany BMG LABTECH Company), laser confocal (Germany Carl Zeiss Company), electric heating constant temperature water bath (Guohua Electric Co., Ltd., HH- 4 digital...
Embodiment 2
[0101] Embodiment 2: Therapeutic effect on cerebral ischemia-reperfusion
[0102] 1. Experimental method
[0103] 1. Nerve cell culture and passage
[0104] (1) Nerve cell recovery
[0105] Take out the nerve cells (N2a cells) frozen in the liquid nitrogen tank, thaw them quickly in a water bath preheated to 37 ° C, and transfer the cells to 9 ml of DMEM medium containing 10% serum under aseptic conditions for centrifugation centrifuge at 1000rmp for 4min. Discard the supernatant, resuspend the cells in 1mL of the above medium, and then transfer to a culture dish containing a new medium, gently blow off the cells with a pipette gun to make them evenly distributed in the culture dish, and place at 37°C , 5%CO 2 Conditioned culture, change the medium after 24h.
[0107] Discard the culture medium in the culture dish, wash once with PBS solution, add 1ml of trypsin, place the culture dish in the cell culture incubator for 1min, when the cells shr...
Embodiment 3
[0124] Embodiment 3: to the therapeutic effect of renal ischemia-reperfusion
[0125] 1. Experimental method
[0126] 1. Kidney epithelial cell culture and passage
[0127] (1) Recovery of renal epithelial cells
[0128] Take out the renal epithelial cells (HK2 cells) frozen in the liquid nitrogen tank, thaw them quickly in a water bath preheated to 37°C, and transfer the cells to 9ml of DMEM medium containing 10% serum under aseptic conditions. In a centrifuge tube, centrifuge at 1000rmp for 4min. Discard the supernatant, resuspend the cells in 1mL of the above medium, and then transfer to a culture dish containing a new medium, gently blow off the cells with a pipette gun to make them evenly distributed in the culture dish, and place at 37°C , 5%CO 2 Conditioned culture, change the medium after 24h.
[0130] Discard the culture medium in the culture dish, wash once with PBS solution, add 1ml of trypsin, place the culture dish in the cell cul...
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