Application of oridonin in preparation of cardiac remodeling resistant medicines
A technology of oridonin and cardiomyocytes, applied in the field of medicine and cell biology, to achieve the effects of low cardiotoxicity, delaying cardiomyocyte hypertrophy, and less drug dosage
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Embodiment 1
[0030] Embodiment 1 Rubescensine A detects the toxicity of isolated cardiomyocytes
[0031] (1) Primary cardiomyocyte culture
[0032] The SD suckling mice within 3 days after birth were disinfected with 75% alcohol, and the heart was removed by opening the chest on the ultra-clean workbench, washed with DMEM / F12 medium and cut into 1-2mm 3 Add 8ml of diluted trypsin digestion solution, heat in a water bath on a magnetic stirrer at a speed of 150rpm, digest for 15 minutes, rest for a few seconds and discard the supernatant containing impurities, then repeat the digestion step and absorb the cardiomyocyte digestion solution, add In the pre-cooled DMEM / F12 medium containing 20% FBS, the digestion was repeated 4-5 times, and the collected cardiomyocyte suspension was collected.
[0033] Centrifuge the collected cardiomyocyte suspension at 1500rpm for 8 minutes, discard the supernatant and add an appropriate amount of medium to resuspend the cells, then filter through a 40μm filt...
Embodiment 2
[0046] Example 2 Effect of Rubescensine A on Hypertrophy of Isolated Cardiomyocytes
[0047] Myocardial remodeling is manifested as an increase in the volume of cardiomyocytes at the cellular level, and the increase in cell volume is mainly due to the abnormal transcription of hypertrophy-related genes caused by various factors. Isolated neonatal rat cardiomyocytes can represent the pathophysiological changes in somatic cells to a certain extent; Ang II is the main neurohumoral stimulating factor when the heart is subjected to long-term excessive pressure load and the renin-angiotensin system is activated. Stimulating isolated cardiomyocytes with Ang II can better simulate the process of myocardial remodeling in vivo, and it can be used to observe the protective effect of oridonin on myocardial cell remodeling under pressure load. The specific simulation and verification process of this embodiment is as follows:
[0048] (1) Primary cardiomyocyte culture
[0049] As in Examp...
Embodiment 3
[0059] Example 3 Effect of In Vivo Application of Oridonin on Myocardial Hypertrophy Caused by Pressure Overload
[0060] (1) Establishment of pressure overload myocardial remodeling model in mice and administration of oridonin
[0061] A pressure load-induced myocardial remodeling model was established by thoracic aortic coarctation. Male C57 mice aged 8-10 weeks and weighing 23.5-27.5g were included in the experiment, and were randomly divided into 4 groups, with 10-12 mice in each group, as follows:
[0062] ①Sham operation without drug treatment group (Sham Veh),
[0063] ②Sham-operated oridonin-administered group (Sham Ori);
[0064] ③ AB operation without medication group (AB Veh),
[0065] ④ AB surgery oridonin A administration group (AB Ori).
[0066]Among them, in the AB operation group (including the AB operation without drug addition group and the AB operation oridonin A administration group), the mice were anesthetized, skin prepared, non-invasive tracheal intu...
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