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红花籽提取物通过阻断核因子κB信号通路减轻骨关节炎的发展。

Safflower Seed Extract Attenuates the Development of Osteoarthritis by Blocking NF-κB Signaling.

作者信息

Han Seong Jae, Lim Min Ju, Lee Kwang Min, Oh Eunjeong, Shin Yu Su, Kim Seokho, Kim Joong Sun, Yun Seung Pil, Kang Li-Jung

机构信息

Department of Biomedical Sciences, Ajou University Graduate School of Medicine, Suwon 16499, Korea.

Department of Pharmacology, Ajou University School of Medicine, Suwon 16499, Korea.

出版信息

Pharmaceuticals (Basel). 2021 Mar 12;14(3):258. doi: 10.3390/ph14030258.

Abstract

Although safflower seed extract exhibits pharmacological activity against various diseases, the effects of its individual compounds on osteoarthritis (OA) have not been elucidated. Here, we evaluated the effects of these extracts and their single compounds on OA. N-(p-Coumaroyl) serotonin and N-feruloyl serotonin, main components of safflower seed extract, were isolated by high-performance liquid chromatography. Under in vitro OA mimic conditions, the expression of the matrix metalloproteinases (MMPs) MMP3/13 and a disintegrin and metalloproteinase with thrombospondin motifs (ADAMTS) ADAMTS5 were reduced in mouse chondrocytes treated with safflower seed extract. Furthermore, the oral administration of safflower seed extract attenuated cartilage destruction in a mouse OA model induced by destabilization of the medial meniscus. N-(p-Coumaroyl) serotonin and N-feruloyl serotonin, but not serotonin, reduced MMP3, MMP13, and ADAMTS5 expression in IL-1β-treated chondrocytes. Additionally, they significantly blocked the nuclear factor-κB (NF-κB) pathway by inhibiting IκB degradation and p65 phosphorylation. Our results suggest that safflower seed extract and its single compounds can attenuate cartilage destruction by suppressing MMP and ADMATS5 expression. The anti-arthritic effects are mediated by NF-κB signaling and involve the inhibition of IκB degradation and p65 phosphorylation. These results indicate that safflower seed extract may serve as a novel therapeutic agent against OA.

摘要

尽管红花籽提取物对多种疾病具有药理活性,但其单个化合物对骨关节炎(OA)的影响尚未阐明。在此,我们评估了这些提取物及其单一化合物对OA的影响。通过高效液相色谱法分离出红花籽提取物的主要成分N-(对香豆酰基)血清素和N-阿魏酰基血清素。在体外OA模拟条件下,用红花籽提取物处理的小鼠软骨细胞中基质金属蛋白酶(MMPs)MMP3/13以及含血小板反应蛋白基序的解聚素和金属蛋白酶(ADAMTS)ADAMTS5的表达降低。此外,口服红花籽提取物可减轻内侧半月板不稳定诱导的小鼠OA模型中的软骨破坏。N-(对香豆酰基)血清素和N-阿魏酰基血清素而非血清素可降低白细胞介素-1β处理的软骨细胞中MMP3、MMP13和ADAMTS5的表达。此外,它们通过抑制IκB降解和p65磷酸化显著阻断核因子-κB(NF-κB)信号通路。我们的结果表明,红花籽提取物及其单一化合物可通过抑制MMP和ADMATS5表达减轻软骨破坏。其抗关节炎作用由NF-κB信号介导,涉及抑制IκB降解和p65磷酸化。这些结果表明,红花籽提取物可能作为一种新型的OA治疗药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc76/7999399/a6442cb9a190/pharmaceuticals-14-00258-g001.jpg

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