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鉴定核桃提取物对 E3 连接酶 Syvn1 的抑制活性。

Identification of the inhibitory activity of walnut extract on the E3 ligase Syvn1.

机构信息

Institute of Medical Science, Tokyo Medical University, Tokyo 160‑8402, Japan.

Institute of Medical Science, St. Marianna University School of Medicine, Kawasaki, Kanagawa 216‑8511, Japan.

出版信息

Mol Med Rep. 2018 Dec;18(6):5701-5708. doi: 10.3892/mmr.2018.9576. Epub 2018 Oct 23.

DOI:10.3892/mmr.2018.9576
PMID:30365055
Abstract

Synoviolin (Syvn1), an E3 ubiquitin ligase in endoplasmic reticulum‑associated protein degradation, is involved in rheumatoid arthritis, fibrosis, liver cirrhosis and obesity. We previously demonstrated that Syvn1 negatively regulates the function of peroxisome proliferator‑activated receptor gamma coactivator‑1β (PGC‑1β). In addition, treatment with a Syvn1 inhibitor suppressed weight gain in a mouse model of obesity by activating PGC‑1β via Syvn1 inhibition. It has been suggested that the Syvn1 inhibitors may have therapeutic benefits in obese patients. The present study tested the inhibitory activity of walnut extract, a natural product, on Syvn1 activity. Walnut extract inhibited the effect of Syvn1 on the cell proliferation of rheumatoid synovial cells and repressed the interaction between PGC‑1β and Syvn1 in an in vitro binding assay. Polyubiquitination of PGC‑1β by Syvn1 was suppressed by walnut extract in a concentration‑dependent manner, but walnut extract did not have an inhibitory effect on the autoubiquitination of Syvn1. Treatment with walnut extract in mouse embryonic fibroblasts increased the number of mitochondria, suggesting that exposure to the extract recovered PGC‑1β function. These results demonstrated that constituents of walnut extract may serve as lead compounds in drug development efforts aiming to produce drugs to treat patients with obesity and obesity‑associated metabolic diseases.

摘要

滑膜凝蛋白 (Syvn1) 是内质网相关蛋白降解过程中的 E3 泛素连接酶,与类风湿性关节炎、纤维化、肝硬化和肥胖有关。我们之前的研究表明,Syvn1 负调控过氧化物酶体增殖物激活受体γ共激活因子 1β (PGC-1β) 的功能。此外,通过 Syvn1 抑制激活 PGC-1β,Syvn1 抑制剂的治疗可抑制肥胖小鼠模型的体重增加。有研究表明,Syvn1 抑制剂可能对肥胖患者具有治疗益处。本研究检测了天然产物胡桃提取物对 Syvn1 活性的抑制活性。胡桃提取物抑制了 Syvn1 对类风湿性滑膜细胞增殖的影响,并在体外结合测定中抑制了 PGC-1β 与 Syvn1 之间的相互作用。胡桃提取物以浓度依赖的方式抑制 Syvn1 对 PGC-1β 的多泛素化,但胡桃提取物对 Syvn1 的自泛素化没有抑制作用。在小鼠胚胎成纤维细胞中用胡桃提取物处理可增加线粒体的数量,表明暴露于提取物可恢复 PGC-1β 的功能。这些结果表明,胡桃提取物的成分可能作为药物开发的先导化合物,旨在开发治疗肥胖症和肥胖相关代谢性疾病患者的药物。

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