Application of dyz-9 in the preparation of anti-cardiac hypertrophy products
A DYZ-9, 1. The technology of DYZ-9 is applied in the application field of preparing anti-cardiac hypertrophy products, which can solve the problems of unreported research and poor effect of reversing ventricular hypertrophy, achieve mature preparation technology and improve clinical cure rate and long-term survival rate, the effect of low production cost
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Embodiment 1
[0034] Example 1: Establishment of an animal model of cardiac hypertrophy and testing the efficacy of DYZ-9 against cardiac hypertrophy
[0035] 1. Materials and methods
[0036] 1. Collection and preparation of specimens: (1) 8-week-old male ICR mice were selected, and the drug isoproterenol (ISO, 5 mg / kg / day) was pumped continuously subcutaneously, and DYZ-9 (1, 10 mg / kg / day) was given at the same time. / day) intraperitoneal injection once a day for a total of 2 weeks. (2) Divide all mice into 4 groups, i.e. control group (Control group, healthy mice without cardiac hypertrophy), isoproterenol group (ISO group), low dose DYZ-9 treatment group (DYZ-9 1mg / kg+ISO group), high-dose DYZ-9 treatment group (DYZ-9 10mg / kg+ISO group).
[0037] 2. The thickness of the left ventricle and the mass index of the left ventricle were measured by echocardiography; the heart and body weight were measured after the animals were sacrificed.
Embodiment 2
[0049]Example 2: Establishment of hypertrophy model of isolated cardiomyocytes and research on the mechanism of action of DYZ-9 against cardiac hypertrophy
[0050] 1. Materials and methods
[0051] 1. The rat cardiomyocyte cell line (H9C2) was stimulated with ISO (10 μM) in vitro to establish a hypertrophy model of cardiomyocytes in vitro. Treatment group DYZ-9 (20 μM, 50 μM, 100 μM) was co-incubated with ISO for 24 hours.
[0052] 2. α-SMA immunofluorescence to observe the morphology of H9C2 cells.
[0053] 3. Real-time quantitative PCR method was used to detect the mRNA expression levels of ANP and BNP in H9C2 cells.
[0054] 4. Western blot detection of p-Akt, Akt, p-CREB, CREB protein expression levels.
[0055] 2. Experimental results
[0056] 1. Immunofluorescence α-SMA detection showed that ISO stimulation can significantly increase the volume of H9C2 cells, while DYZ-9 can reverse it ( Figure 4 A, B).
[0057] 2. Compared with the normal control group, ISO (10μ...
Embodiment 3
[0059] Example 3: Verification of the DYZ-9 target at the whole animal level
[0060] 1. Materials and methods
[0061] 8-week-old male ICR mice were selected, subcutaneously pumped into the drug isoproterenol and intraperitoneally injected with DYZ-9 (1, 10 mg / kg / day) once a day, and sacrificed for a total of 2 weeks. The mice were detected by Western blot p-Akt, Akt protein expression level.
[0062] 2. Experimental results
[0063] DYZ-9 treatment could significantly reverse the increase in the phosphorylation levels of Akt and CREB in mouse heart tissue caused by ISO ( Figure 7 A, B).
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