Application of Neogenin to preparation of medicine for preventing, relieving and/or treating myocardial infarction and related diseases thereof
A technology for myocardial infarction and ischemic cardiomyopathy, applied to the multifunctional transmembrane receptor neogenin, the application of medicines for relieving and/or treating myocardial infarction and its related diseases, and the preparation of preventive fields, which can solve problems such as unclear effects
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experiment example 1
[0026] Experimental example 1Neo1 neutralizing antibody aggravates cardiac function after myocardial infarction
[0027] 1. Inject Neo1 neutralizing antibody
[0028] Neo1 neutralizing antibody (product number AF1079) was purchased from RD Company in the United States, which can effectively bind to the receptor Neo1, block the interaction between Neo1 and its related ligands, and complete the function inhibition of Neo1 in vivo. Two hours before myocardial infarction, the mice were fixed, and Neo1 neutralizing antibody (the solvent was saline) was injected through the tail vein at a dose of 2 μg / mouse, and the control group was given a placebo (vehicle, saline). The experiment was divided into 4 groups according to the random and blind principle: no operation (sham)+vehicle, sham+Anti-Neo1, myocardial infarction group (MI)+vehicle, MI+Anti-Neo1.
[0029] 2. Myocardial infarction model acquisition
[0030] (1) Anesthetized by intraperitoneal injection of 3% pentobarbital sodi...
experiment example 2
[0040] Experimental example 2Neo1 neutralizing antibody increases infarct size and aggravates myocardial remodeling after myocardial infarction
[0041] 1. 2,3,5-Triphenyltetrazolium chloride (2,3,5-Triphenyltetrazolium chloridej, TTC) staining
[0042] (1) After the mice were sacrificed 3 days after myocardial infarction, the heart tissue was quickly taken out and placed in 10% KCl solution.
[0043] (2) After washing the heart, place it in a -20°C refrigerator for 30 minutes.
[0044] (3) The heart tissue was taken out and sliced uniformly along the long axis of the heart from the apex to the bottom of the heart. The slices were immediately placed in 10 mL of 2% TTC solution and incubated at a constant temperature of 37°C for 20 min. Normal heart tissue stained bright red, while the infarct area was pale.
[0045] (4) The brain tissue slices were fixed with 10% neutral formalin solution, the gross photographs were taken, and the infarct area was calculated.
[0046] 2. ...
experiment example 3
[0108] Experimental example 3Neo1 neutralizing antibody aggravates cardiomyocyte apoptosis after myocardial infarction
[0109] 3.1 Western Blot monitoring of apoptosis-related proteins
[0110] Protein extraction, electrophoresis gel as above, using the primary antibodies Bax, Bcl-2 and GAPDH.
[0111] 3.2 Immunofluorescence
[0112] 3.2.1 Preparation of paraffin specimens and sections
[0113] (1) The mouse heart tissue was taken out from the 10% formalin solution, the heart tissue was trimmed in a fume hood, and the trimmed heart tissue and the corresponding label were placed in a dehydration box.
[0114] (2) Dehydration and wax dipping: Put the dehydration box into the dehydrator for dehydration and wax dipping treatment. 75% ethanol (4h)→85% ethanol (2h)→90% ethanol (2h)→95% ethanol (1h)→absolute ethanol I (30min)→absolute ethanol II (30min)→alcohol benzene (5-10min )→xylene I (5-10min)→xylene II (5-10min)→65°C melted paraffin I (1h)→65°C melted paraffin II (1h)→65°C...
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