Application of syringic acid in preparation of medicine for treating osteoarthritis caused by cartilage degradation
A technology for osteoarthritis and cartilage degradation, applied in the direction of drug combinations, antipyretics, anti-inflammatory agents, etc., can solve the problems of inherent mechanical and biochemical properties, easy to break, etc., achieve low immunogenicity, easy synthesis, Mitigate the effect of progression
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Embodiment 1
[0030] This example provides the ability of syringic acid to promote the expression of type II collagen and aggrecan in chondrocytes in vitro;
[0031] Including the following steps:
[0032] Step 1, in vitro isolation and extraction of primary mouse articular chondrocytes for culture;
[0033] Step 2, intervene chondrocytes with different concentrations of syringic acid;
[0034] Step 3, using CCK8 method to observe its toxic and side effects on chondrocytes. The results of CCK8 as figure 1 shown.
[0035] Specifically, it mainly includes: cell seeding plate, first intervening cells with 50uM syringic acid for 24 hours, extracting total RNA, and performing fluorescent quantitative PCR to detect the effect of syringic acid on chondrocyte type 2 collagen (COL2) and aggrecan (aggrecan; ACAN) expression;
[0036] Intervene chondrocytes with lipopolysaccharide 1ug / ml or lipopolysaccharide plus 50uM syringic acid, extract total RNA, and perform fluorescent quantitative PCR to ...
Embodiment 2
[0039] This example provides the ability of syringic acid to improve the microenvironment in vivo and reduce the progression of osteoarthritis in mice;
[0040] Including the following steps:
[0041] Twenty C57BL / 6 female mice were randomly divided into sham operation group (sham), model group (DMM), low-dose SA group (SA-L) and high-dose SA group (SA-H), 5 in each group, A mouse osteoarthritis model was established in vivo, and the medial meniscus (DMM) of the right mouse knee joint was resected. After operation, the mice in the DMM+low-dose SA group and the DMM+high-dose SA group were treated with 0.3mg / kg and 1.5mg / kg respectively. Carry out intra-articular injection, once every three days, and the other groups are given equal volume of PBS, and the mice are sacrificed after 4 weeks;
[0042] The above four groups (sham, DMM, SA-L, SA-H) were subjected to safranin fast green and toluidine blue fast green histological staining analysis, the results are as follows image 3...
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