Biomarker having high-blood coagulation status and application of same
A state-marking and hypercoagulable technology, applied in the field of biomarkers of hypercoagulation state, can solve problems such as no research reports on urine biomarkers
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Embodiment 1
[0072] Embodiment 1, establishment of rat acute hypercoagulation state model
[0073] 1. Constructing an animal model of hypercoagulable state in rats based on phensulfame
[0074] 1. Experimental method
[0075] Twenty male wistar rats were randomly divided into two groups, 10 in each group, and weighed. One group of rats was intraperitoneally injected with phensulfame injection (250 mg / kg body weight), and was recorded as the experimental group; the other group of rats was injected with a corresponding volume of normal saline injection, and was recorded as the control group. The time of the first injection was recorded as 0h, and intraperitoneal injection was performed every 3h, for a total of 3 injections (that is, once at 0h, 3h and 6h). 9 hours after the first injection (i.e. 3 hours after the third injection), blood was collected from the inner canthus vein immediately, and the coagulation function of the rat was detected to determine the specifications for the formati...
Embodiment 2
[0090] Example 2. Urinary proteomics analysis and biomarker research in hypercoagulable state
[0091] 1. Experimental method
[0092] 1. Extraction of urine proteome by ethanol precipitation
[0093] Get the urine sample of the rat hypercoagulation state animal model based on different coagulation-promoting drugs (acetamine, tranexamic acid and aminocaproic acid) in Example 1 as the experimental group sample, and simultaneously use the control in each model The urine sample of the group was used as the control sample, and the protein group in the urine sample was extracted. The specific extraction method is as follows: Take 8 mL of urine sample in a clean 50 mL centrifuge tube, centrifuge: 2500 g, 30 min, 4 °C. Transfer the supernatant to a clean 50mL centrifuge tube, centrifuge: 12000g, 30min, 4°C. Measure the volume of the supernatant, transfer it to a clean 50mL centrifuge tube, add three times the volume of -20°C pre-cooled absolute ethanol, shake well, and settle at -20...
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