Advanced glycosylation end product CML as early diagnosis marker of myocardial ischemia reperfusion injury and application thereof
A technology of advanced glycation and reperfusion injury, applied in the field of reducing myocardial ischemia-reperfusion injury, early diagnosis markers of myocardial ischemia-reperfusion injury, and achieving the effect of reducing myocardial ischemia-reperfusion injury
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Embodiment 1
[0038] Example 1 Establishing a mouse model of ischemia-reperfusion injury and detecting the level of advanced glycation end product CML
[0039] Experimental materials: 7-8 weeks wild-type C57B / 6 mice, CML antibody (ab27684, abcam, USA), CML detection kit (OxiSelect TM Nε-(carboxymethyl)lysine (CML) Competitive ELISA Kit, CellBiolabs, USA)
[0040]Methods: 1) 7-8 weeks old wild-type C57B / 6 mice were taken, anesthetized with 2% isoflurane, opened the left chest cavity of the mice, ligated the anterior descending branch with 6-0 suture to cause myocardial ischemia, and loosened after 40 minutes. After the thread knot was opened, the myocardial tissue and peripheral blood of the mouse were taken 2 hours, 24 hours, and 48 hours after the thread knot was loosened to detect the CML level. 2) For the detection method of CML in peripheral blood, please refer to the instructions of the CML detection kit. 3) Myocardial tissue CML detection method: extract myocardial tissue protein, ...
Embodiment 2
[0042] Example 2 Effect of CML on cardiac function and infarct size in mice
[0043] Experimental materials: 7-8 weeks old wild-type C57B / 6 mice, CML reagent, Evans blue dye, TTC dye
[0044] Methods: 1) 7-8 weeks old wild-type C57B / 6 mice were taken, anesthetized with 2% isoflurane, opened the left chest cavity of the mice, ligated the anterior descending branch with 6-0 suture to cause myocardial ischemia, and loosened after 40 minutes. Open the thread knot, inject 0.1mg / kg CML locally with the myocardial tissue, and suture the chest cavity; 2) 24 hours later, use the VisualSonics VeVo 2100 imaging system to detect the mouse heart function; 3) 2% isoflurane anesthetize the mouse, open the chest cavity, Use 1% Evans blue dye to perfuse the mouse heart, remove the mouse heart, cut it into 4-5 pieces, put it into a petri dish filled with 1% TTC, incubate at 37 degrees for 30 minutes, in the asana The area of myocardial infarction was observed under a microscope.
[0045] Re...
Embodiment 3
[0046] Example 3 Effects of Pyridorin on Cardiac Function and Infarct Size in Myocardial Ischemia-Reperfusion Injury Model Mice
[0047] Experimental materials: 6-7 weeks wild type C57B / 6 mice, pyridorin drug, Evans blue dye, TTC dye
[0048] Methods: 1) Take wild-type C57B / 6 mice at 6-7 weeks, add Pyridorin (1g / L) to their drinking water and feed them for a week, and use the above method to establish a myocardial ischemia-reperfusion model; 2) After 24 hours, , VisualSonics; VeVo2100 imaging system was used to detect the cardiac function of mice; 3) The infarct area of mice was observed by the above method.
[0049] Results: Pyridorin can effectively improve the cardiac function and myocardial infarct size after ischemia-reperfusion injury in mice. (Fig. 5, 6)
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