Method for detecting platelet nmda receptor activity and application thereof
A technology of platelets and receptors, applied in the field of medical biology, can solve the problems of affecting the functional activity of platelets, platelet adhesion and aggregation functions have not been reported, and achieve the effect of reducing platelet aggregation
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Embodiment 1
[0025] Platelets of Example 1 Human and Mouse Express NMDA Receptors
[0026]
[0027] ICR mice (10 males and 10 females each), weighing 25-30 grams, were purchased from the Experimental Animal Center of Jiangsu Province. Use a 3.8wt.% citrate anticoagulant tube to extract 2 mL of blood from the human cubital vein or the inner canthus of mice (the volume ratio of blood:anticoagulant is 1:9), mix it and place it at room temperature for low-speed centrifugation at 800 r / min After 8 minutes, carefully remove the upper layer of plasma, which is platelet-rich plasma (PRP). The remaining blood sample was then centrifuged at 3000r / min for 10 minutes, and the clear liquid on the upper layer was platelet poor plasma (PPP).
[0028]
[0029] Five subunits of NMDA receptors, NMDA receptor 1 and NMDA receptor 2 (A-D), have been cloned so far. Among them, NMDA receptor 1 can form functional pure oligomer NMDA receptor alone, but NMDA receptor 2 subunit does not have this function. T...
Embodiment 2
[0033] Ca of embodiment 2 platelet NMDA receptor 2+ inflow.
[0034]
[0035] With embodiment 1.
[0036] Selective NMDA receptor agonists N-methyl-D-aspartic acid (NMDA) and glutamate (glutamate), selective NMDA receptor antagonists MK-801 and memantine were purchased from Sigma.
[0037]
[0038] platelet free Ca 2+ ([Ca 2+ ] i) Concentration determination: Ca 2+ For fluorescent probe loading, the platelet-rich plasma suspension was centrifuged at 1000 r / min, 10 minutes each time x 3 times, the supernatant was sucked out and mixed by pipetting. Take 50 μL of cell suspension, add 17 μL of Fura-2 calcium probe, and incubate in a water bath at 36.5°C for 40 minutes. Fluorescence dual-wavelength spectrophotometer determination of [Ca 2 + ] i, The fluorescence intensity of Fura-2 was measured with a Hitachi F-3000 fluorescence dual-wavelength spectrophotometer. The measurement conditions are: the excitation light grating is 5nm, the emission light grating is 10nm, an...
Embodiment 3
[0045] Example 3 NMDA receptor activation can promote platelet adhesion.
[0046]
[0047] With embodiment 1 and embodiment 2.
[0048]
[0049] Platelet adhesion test method: suck out 1.5mL of anticoagulant blood, pour it into a long-necked glass bottle and insert it to the bottom, then take blood from it to calculate the number of platelets before rotation, and calculate the average number of two or three times as the number of platelets before rotation. After the flask was inserted into the platelet adhesion analyzer, it was rotated for 15 minutes at a rate of 3 revolutions per minute, and then blood was taken from the flask. The platelets were counted two or three times according to the conventional method, and the average value was calculated as the number of platelets after rotation. (number of platelets before rotation-number of platelets after rotation) / number of platelets before rotation=platelet adhesion rate.
[0050] Add NMDA receptor agonist NMDA (0-100 μM) o...
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