Function and application of A20 combined nuclear factor profilin 1(ABIN1) in cardiac hypertrophy treatment
A technology to inhibit protein and cardiac hypertrophy, applied in the field of gene function and application, to achieve the effect of protecting heart function
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Embodiment 1
[0059] The establishment of embodiment 1 mouse myocardial hypertrophy model
[0060] Aortic arch constriction (AB) was used to establish a mouse model of myocardial hypertrophy, and the operation procedure of the model was as follows:
[0061] 1.1 Animal selection
[0062] Wild-type mice (WT), ABIN1 knockout mice (ABIN1-KO), cardiac-specific ABIN1 transgenic mice (ABIN1-TG) and non-transgenic mice aged 8-10 weeks and weighing 23.5-27.5 g were selected. Mice (NTG) were divided into sham operation group (sham) and AB myocardial hypertrophy model group, that is, WTsham group, WTAB group, ABIN1-KOsham group, ABIN1-KOAB group, ABIN1-TGsham group, ABIN1-TGAB group, NTGsham group, NTGAB group, 10 mice in each group.
[0063] 1.2 Preoperative preparation
[0064] (1) Anesthesia: First weigh the mice, calculate the required amount of anesthetic (3% pentobarbital sodium) according to 90 mg / kg body weight, inject intraperitoneally, and record the injection time point. There is no obv...
Embodiment 2
[0072] Example 2 Detection of cardiac hypertrophy and fibrosis in myocardial hypertrophy model mice
[0073] 1. Take materials
[0074] (1) Preliminary work: prepare in advance a urine cup filled with 20mL of 10% formaldehyde by volume, and label it (mouse number, group, type of operation and date of collection). Place a petri dish filled with 10% KCl solution in mass fraction at the sampling site. Turn on the analytical balance and set it to zero for later use. Mice were then weighed and sacrificed.
[0075] (2) Material collection: Ophthalmic curved forceps clamped the vascular pedicle below the atrial appendage, cut off the heart, and quickly placed it in a 10% KCl solution. After the heart stops beating in the diastolic phase, place it on sterilized gauze, gently squeeze the fluid in the heart cavity, dip the surface fluid dry, weigh and record, put the heart into the corresponding urine cup, fix it for 48 hours and use it for pathological testing.
[0076] (3) Releva...
Embodiment 3
[0091] Example 3 Cardiac Function Detection of Myocardial Hypertrophy Model Mice
[0092] Ultrasound testing of heart function
[0093] 1. Preliminary preparation
[0094] (1) Anesthesia machine preparation: first connect the oxygen cylinder and the air inlet port on the anesthesia machine, then unscrew the sealing cap of the dosing port on the anesthesia machine, quickly add isoflurane to the safety scale, and then tighten the sealing cap. Unscrew the main valve on the oxygen cylinder, adjust the knob of the flow control valve, and maintain the outlet pressure at 0.2-0.3mPa.
[0095] (2) Preparation of the mice to be tested: After the mice to be tested were quickly anesthetized with isoflurane, the hair on the left chest area was shaved, and the head of the treated mice was inserted into the anesthetic catheter sleeve, and treated with 1.5-2.0% isoflurane Alkane maintains a stable state of anesthesia in mice.
[0096] 2. Cardiac function test
[0097] The mice were placed...
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