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皱边石莼乙醇提取物中的倍半萜类化合物通过抑制核因子 κB 的激活抑制胶原诱导的 DBA/1J 小鼠类风湿关节炎。

Meroterpenoid-Rich Fraction of the Ethanol Extract of Sargassum Serratifolium Suppresses Collagen-Induced Rheumatoid Arthritis in DBA/1J Mice Via Inhibition of Nuclear Factor κB Activation.

机构信息

Department of Food Science and Nutrition, Pukyong National University, 45 Yongso-ro, Nam-gu, Busan, 48513, Republic of Korea.

Department of Pathobiological Science, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA, 70802, USA.

出版信息

Mol Nutr Food Res. 2020 Feb;64(3):e1900373. doi: 10.1002/mnfr.201900373. Epub 2020 Jan 10.

Abstract

SCOPE

Rheumatoid arthritis (RA) is an autoimmune disorder related to the inflammation of cartilage due to the infiltration of inflammatory cells. Sargassum serratifolium, a brown alga, possesses strong anti-inflammatory activities.

METHODS AND RESULTS

The effect of meroterpenoid-rich fraction from the ethanol extract of S. serratifolium (MES) on RA and its underlying mechanisms on the inhibition of RA using a collagen-induced arthritis (CIA) mouse model are examined. The results show that MES ameliorates paw swelling and reduces the arthritis score. MES considerably decreases the secretion of pro-inflammatory cytokines in the serum and joint tissue of mice. Histopathological analysis demonstrates that MES strongly inhibited bone damage and inflammatory cell intrusion in the joint tissue. The expression of inflammatory enzymes and adhesion molecules is significantly inhibited in the serum and joint tissue of MES-fed mice. In addition, MES downregulates the nuclear factor κB (NF-κB) signaling pathway by suppressing the phosphorylation of protein kinase B, c-Jun N-terminal kinase, and p38 mitogen-activated protein kinases.

CONCLUSIONS

MES supplementation remarkably reduces inflammatory response in CIA mouse model. These results indicate that MES can be used as a pharmaceutical agent against RA.

摘要

范围

类风湿性关节炎(RA)是一种自身免疫性疾病,与软骨炎症有关,炎症细胞浸润是其主要原因。 褐藻马尾藻具有很强的抗炎活性。

方法和结果

本研究考察了马尾藻乙醇提取物中的混合倍半萜类化合物丰富部分(MES)对 RA 的影响及其在胶原诱导性关节炎(CIA)小鼠模型中抑制 RA 的潜在机制。结果表明,MES 可改善爪肿胀并降低关节炎评分。MES 可显著减少小鼠血清和关节组织中促炎细胞因子的分泌。组织病理学分析表明,MES 可强烈抑制关节组织中的骨损伤和炎性细胞浸润。MES 还可抑制炎性酶和粘附分子在血清和关节组织中的表达。此外,MES 通过抑制蛋白激酶 B、c-Jun N 末端激酶和 p38 丝裂原活化蛋白激酶的磷酸化来下调核因子 κB(NF-κB)信号通路。

结论

MES 补充剂可显著减轻 CIA 小鼠模型中的炎症反应。这些结果表明,MES 可用作治疗 RA 的药物。

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