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首页> 外文期刊>Journal of pharmacological sciences. >Effects of Flavonoids on Matrix Metalloproteinase-13 Expression of Interleukin-1β–Treated Articular Chondrocytes and Their Cellular Mechanisms: Inhibition of c-Fos/AP-1 and JAK/STAT Signaling Pathways
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Effects of Flavonoids on Matrix Metalloproteinase-13 Expression of Interleukin-1β–Treated Articular Chondrocytes and Their Cellular Mechanisms: Inhibition of c-Fos/AP-1 and JAK/STAT Signaling Pathways

机译:黄酮类化合物对白介素-1β处理的关节软骨细胞基质金属蛋白酶-13表达的影响及其细胞机制:抑制c-Fos / AP-1和JAK / STAT信号通路

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References(37) Cited-By(11) To identify the therapeutic potential for cartilage degradation and its action mechanisms, the effects of naturally-occurring flavonoids on matrix metalloproteinase-13 (MMP-13) induction were examined in the human chondrocyte cell line SW1353. Flavones including apigenin and wogonin strongly inhibited MMP-13 induction in interleukin (IL)-1β–treated SW1353 cells, while flavonols such as kaempferol, quercetin, and flavanone (naringenin) did not at 5 – 25 μM. Apigenin and wogonin primarily inhibit MMP-13 by blocking the c-Fos / activator protein-1 (AP-1) and Janus kinase 2 (JAK2) / signal transducer and activator of transcription 1/2 (STAT1/2) pathways, but not nuclear factor-κB (NF-κB) signaling. Apigenin was also shown to inhibit extracellular matrix degradation in rabbit cartilage culture. The following study using some synthetic flavones demonstrated that A-ring C-5,7-dihydroxyl and B-ring dihydroxyl substitution at C-2,3, C-2,4, or C-3,4 are important for the suppression of MMP-13 expression. Among these flavones, 2′,3′,5,7-tetrahydroxyflavone also inhibited both the c-Fos/AP-1 and STAT1/2 pathways. Taken together, these results indicate that certain flavonoids, especially flavones, inhibit MMP-13 expression in IL-1β–treated chondrocytes, at least in part, by suppressing the c-Fos/AP-1 and JAK2/STAT1/2 pathways. Furthermore, these findings suggest that some flavonoids have the potential for protecting against collagen matrix breakdown in the cartilage of diseased tissues such as those found in arthritic disorders.
机译:参考文献(37)被引用的文献(11)为了确定软骨降解的治疗潜力及其作用机制,在人类软骨细胞系SW1353中研究了天然类黄酮对基质金属蛋白酶13(MMP-13)诱导的作用。 。黄酮包括芹菜素和沃戈宁在白介素(IL)-1β处理的SW1353细胞中强烈抑制MMP-13诱导,而黄酮醇(如山emp酚,槲皮素和黄烷酮(柚皮苷)的浓度为5 – 25μM)则没有。芹菜素和Wogonin主要通过阻断c-Fos /激活蛋白1(AP-1)和Janus激酶2(JAK2)/信号转导子和转录激活子1/2(STAT1 / 2)途径来抑制MMP-13,但不是核因子-κB(NF-κB)信号传导。芹菜素还显示出在兔软骨培养物中抑制细胞外基质降解。以下使用某些合成黄酮的研究表明,在C-2,3,C-2,4或C-3,4处的A环C-5,7-二羟基和B环二羟基取代对于抑制C MMP-13表达。在这些黄酮中,2',3',5,7-四羟基黄酮也抑制c-Fos / AP-1和STAT1 / 2途径。综上所述,这些结果表明,某些类黄酮,尤其是黄酮,至少部分地通过抑制c-Fos / AP-1和JAK2 / STAT1 / 2途径来抑制IL-1β处理的软骨细胞中MMP-13的表达。此外,这些发现表明,某些类黄酮具有预防疾病组织(例如关节炎疾病中)的软骨中胶原蛋白基质分解的潜力。

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