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帕奇米酸通过调节 Sirtuin 6/NF-κB 信号轴抑制软骨细胞的炎症反应,缓解骨关节炎的进展。

Pachymic acid suppresses the inflammatory response of chondrocytes and alleviates the progression of osteoarthritis via regulating the Sirtuin 6/NF-κB signal axis.

机构信息

Department of Orthopaedics, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325000, PR China; Zhejiang Provincial Key Laboratory of Orthpaedics, Wenzhou, Zhejiang 325000, PR China; The Second School of Medicine, WenZhou Medical University, Wenzhou, Zhejiang 325000, PR China.

Department of Orthopaedics, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325000, PR China; Zhejiang Provincial Key Laboratory of Orthpaedics, Wenzhou, Zhejiang 325000, PR China; The Second School of Medicine, WenZhou Medical University, Wenzhou, Zhejiang 325000, PR China.

出版信息

Int Immunopharmacol. 2023 Nov;124(Pt A):110854. doi: 10.1016/j.intimp.2023.110854. Epub 2023 Aug 30.

Abstract

Articular cartilage degeneration is a characteristic pathological change of osteoarthritis (OA). Pachymic acid (PA) is an active ingredient found in Poria cocos. Previous studies have shown that PA has anti-inflammatory effects on a variety of diseases. However, the role of PA in OA and its underlying mechanisms has not been clearly elucidated. In this study, we investigated potential protective effect of PA on OA through cell experiments in vitro and animal experiments in vivo. PA inhibited interleukin-1β-induced inflammatory mediator production in chondrocytes, which includes nitric oxide, inducible nitric oxide synthase, prostaglandin E2, cyclooxygenase-2, tumor necrosis factor alpha and interleukin-6. Meanwhile, PA also reversed the up-regulation of matrix metalloproteinase-3 and thrombospondin motifs 5, and the down-regulation of collagen type II and aggrecan in IL-1β-treated chondrocytes. Mechanistically, our findings revealed that PA-mediated overexpression of SIRT6 inhibited the NF-κB signaling pathway. In vivo, PA contributes to improve cartilage damage in the mouse OA model. In summary, PA inhibited IL-1β-induced inflammation and extracellular matrix degeneration by promoting SIRT6 expression and inhibiting the NF-κB signaling pathway, which indicates that PA is beneficial for the treatment of OA.

摘要

关节软骨退变是骨关节炎(OA)的特征性病理改变。茯苓酸(PA)是从茯苓中提取的一种活性成分。先前的研究表明,PA 对多种疾病具有抗炎作用。然而,PA 在 OA 中的作用及其潜在机制尚不清楚。在这项研究中,我们通过体外细胞实验和体内动物实验研究了 PA 对 OA 的潜在保护作用。PA 抑制了软骨细胞中白细胞介素-1β诱导的炎性介质产生,包括一氧化氮、诱导型一氧化氮合酶、前列腺素 E2、环氧化酶-2、肿瘤坏死因子-α和白细胞介素-6。同时,PA 还逆转了白细胞介素-1β处理的软骨细胞中基质金属蛋白酶-3 和血小板反应蛋白基序 5 的上调,以及胶原 II 和聚集蛋白聚糖的下调。从机制上讲,我们的研究结果表明,PA 介导的 SIRT6 过表达抑制了 NF-κB 信号通路。在体内,PA 有助于改善小鼠 OA 模型中的软骨损伤。综上所述,PA 通过促进 SIRT6 的表达和抑制 NF-κB 信号通路,抑制了白细胞介素-1β诱导的炎症和细胞外基质降解,表明 PA 有利于 OA 的治疗。

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