Application of fibroblast growth factor 21
A technology of fibroblasts and growth factors, applied in the medical field
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Embodiment 1
[0021] Example 1 The role of FGF21 in hypoxic pulmonary hypertension
[0022] Experimental method: An in vivo model of hypoxic pulmonary hypertension was constructed, and it was confirmed that FGF21 can inhibit pulmonary hypertension and pulmonary vascular remodeling, and FGF21 plays a protective role by up-regulating the expression level of PPARγ.
[0023] This is done with the following steps:
[0024] Male SD rats were randomly divided into A. normoxia group; B. hypoxia group; C. hypoxia+FGF21 intervention group. The rats in the hypoxia group were all placed in an open-hole hypoxic chamber with standard air pressure, and the O2 was kept at 8%-11%, and the CO2 concentration was kept at <3%. They entered the chamber for 8 hours a day. Group C was intraperitoneally injected with FGF21 400ug / Kg 30 minutes before entering the cabin. Continuous modeling for 4 weeks.
[0025] a. Using the PowerLab physiological record analyzer, the right heart catheterization method was used to...
Embodiment 2
[0029] Example 2 Effect of FGF21 on the proliferation and functional changes of pulmonary artery endothelial cells under hypoxia
[0030] Test method: Construct the hypoxia model of endothelial cells in vitro, and confirm the effect of FGF21 on the proliferation and secretion function of endothelial cells.
[0031] This is done with the following steps:
[0032] 1) Purchase human PAECs, use anti-CD31 monoclonal antibody immunofluorescence staining to identify HPAECs and determine cell purity. PAECs of the same generation were randomly divided into: A. normoxia group; B. hypoxia group; C. hypoxia+FGF21 (800ng / ml) group. All hypoxic groups were cultured in a hypoxic incubator under the conditions of 5% CO2, 5% O2, 90% N2, and 37°C. The normoxic group was cultured in a normoxic incubator under the conditions of 5% CO2, 95% N2, and 37°C. After 48 hours of modeling, it was used for follow-up detection.
[0033] 2) CCK-8 staining method was used to detect the proliferation of PA...
Embodiment 3
[0037] Example 3 Effect of FGF21 on Pulmonary Artery Smooth Muscle Cell Proliferation and Inflammatory Response under Hypoxia
[0038] Test method: By constructing the PASMCs hypoxia model, it was confirmed that FGF21 can inhibit the excessive proliferation of PASMCs under hypoxia, and reduce the secretion levels of IL-1, IL-6, and TNF-α inflammatory factors.
[0039] 1) The primary rat PASMCs were obtained by enzymatic digestion, and the purity of PASMCs was identified by immunofluorescence staining with monoclonal antibody against α-SM actin. PASMCs were randomly divided into: A. normoxia group; B. hypoxia group; C. hypoxia + FGF21 (800ng / ml) group. All the hypoxic groups were in the hypoxic incubator according to the conditions of 5% CO2, 5% O2, 90% N2, 37 ℃, and the normoxia group were in the normoxia incubator according to the conditions of 5% CO2, 95% N2, 37 ℃. Conditions, were cultured for 24 hours before index detection.
[0040] 2) CCK-8 staining was used to detect ...
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