Pharmaceutical composition, for preventing or treating sarcopenia, containing salicornia europaea extract
A technology for sarcopenia and Salicornia grass, applied in drug combinations, medical preparations containing active ingredients, muscular system diseases, etc., can solve problems such as unsuitable for long-term treatment, affecting bone formation and regeneration, and masculinization of women , to achieve the effect of complete prevention or treatment
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Embodiment 1
[0053] Example 1. Verification of the inhibitory effect against sarcopenia caused by UV irradiation
[0054] C2C12 muscle precursor cells (ATCC, US) were cultured in DMEM containing 10% FBS. At this point, the 3x10 5 Cells were seeded in a 60 pie dish. On the second day after sowing, laminarin and fucoidan were treated separately and left for 1 hour. After 1 hour, the growth media (10% FBS DMEM) was removed and washed with PBS. After removing the PBS, after removing the plate cover from the UV cross-linker (UVP CL-1000), perform 3J / m 2 UV irradiation (0 days). After culturing in a CO2 incubator (Incubator) for 24 hours, the growth medium was removed in the same manner, and PBS was washed, followed by 3J / m 2 UV irradiation (1 day).
[0055] On the next day, harvesting was performed at the same time (2 days), and changes in the expression of myostatin and MURF1 proteins, which are target proteins regulating muscle mass, in cell lysates were detected using Western blotting....
Embodiment 2
[0060] Example 2. Verification of the inhibitory effect against sarcopenia caused by bleomycin
[0061] C2C12 muscle precursor cells (ATCC, US) were cultured in DMEM containing 10% FBS. At this point, the 3x10 5 Cells were seeded in a 60 pie dish and, after seeding, treated with bleomycin and left for 1 hour.
[0062] Next, laminarin and fucoidan were treated separately, and after standing for 1 hour, the growth medium (10% FBS DMEM) was removed and washed with PBS. After washing, Western blotting was used to detect the expression changes of myostatin and MURF1 proteins, which are target proteins regulating muscle mass, in the cell lysates. Comparative analysis was performed using anti-GDF8 (Genetex, GTX32624) as myostatin and β-actin antibody (ENOGene E12-041-4) as protein loading control.
[0063] After RNA was isolated using RNeasy-Mini Kit (Qiagen, US) and cDNA was synthesized using AMV Reverse Transcriptase (Promega, US), the degree of myostatin mRNA expression was con...
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