Application of scutellarin to preparing kidney ischemic reperfusion injury preventing/protecting drugs/drug combinations
A technology of ischemia-reperfusion and baicalin, applied in the field of biomedicine, can solve the problem of lack of strong evidence of drug action
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Embodiment 1
[0023] Embodiment 1 scutellarin pretreatment grouping
[0024] Thirty 8-week-old, healthy male SPF Wistar rats weighing 250-300g were housed in isolated cages with independent air supply, the temperature was controlled at 21°C±2°C, the relative humidity was controlled at 50%+15%, and the day and night cycle For 12 hours, eat normally, and change the litter every 2 days. They were randomly divided into 5 groups, namely normal group, sham operation group, AKI group, scutellarin+AKI group, and Saline+AKI group, with 6 rats in each group. Rats in the administration group (scutellarin+AKI group) and the control group (Saline+AKI) were given drug treatment by intraperitoneal injection at the same time every day 7 days before modeling. According to the experimental grouping, scutellarin+AKI The Saline+AKI group and the Saline+AKI group were given scutellarin and an equal volume of normal saline at a dose of 50 mg / kg.d, and the dose was determined by referring to previous experimenta...
Embodiment 2
[0028] Embodiment 2 ischemia-reperfusion model making
[0029]6-8 weeks Wistar rats were cultured at 21°C±2°C, 50%+15% humidity, and 12 hours of light, and were fed with standard pellet feed and sterile water. Rats were kept in a cage of 6 and fasted for 12 hours before surgery. The high-pressure steam sterilizer is set at 120°C for 40 minutes, and the surgical instruments are put in for sterilization. Rats were anesthetized by intraperitoneal injection of pentobarbital sodium (30 mg / kg), and the rats were in a state of complete muscle relaxation, and the anesthesia was successful. The abdomen was placed in a supine position, and the limbs were gently fixed with elastic ropes. La, because the time of anesthesia cannot be determined, the rat may be awake during the operation, and the operator may be bitten if the fixation is not good. Lift the tongue out of the mouth from the side to prevent the animal from suffocating due to the tongue falling back to block the pharynx. Rem...
Embodiment 3
[0031] Embodiment 3 Rat blood creatinine, blood urea nitrogen monitoring
[0032] First anesthetize the animal, and fix it on the surgical rack in a supine position, and incise the abdominal cavity from the midline of the abdomen to expose the inferior vena cava clearly. Use a syringe to insert the blood vessel towards the centrifugal end of the inferior vena cava and suck out the blood. When drawing blood, quickly prevent blood coagulation from blocking the needle tube. Draw 5ml of blood and place it in a 5ml EP tube for 1 hour. Centrifuge at 3000rpm for 15 minutes in a high-speed centrifuge. Transfer the upper serum to a new EP tube for use in blood creatinine and blood urea nitrogen. For detection, store at 4°C. The specimens were sent to the laboratory department of the hospital within 24 hours, and the levels of creatinine and urea nitrogen were detected by enzymatic method. The test results are shown in Table 1.
[0033] Table 1 Rat serum creatinine (μmol / L) result
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