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新型 p38 抑制剂 Pamapimod 抑制破骨细胞生成并拮抗雌激素依赖性小鼠骨丢失。

The Novel p38 Inhibitor, Pamapimod, Inhibits Osteoclastogenesis and Counteracts Estrogen-Dependent Bone Loss in Mice.

机构信息

Department of Orthopaedics, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.

Key Laboratory of Musculoskeletal System Degeneration and Regeneration Translational Research of Zhejiang Province, Hangzhou, China.

出版信息

J Bone Miner Res. 2019 May;34(5):911-922. doi: 10.1002/jbmr.3655. Epub 2019 Jan 7.

Abstract

Pamapimod (PAM) is a novel selective p38 mitogen-activated protein (MAP) kinase inhibitor proved to be effective in rheumatoid arthritis in phase 2 clinical trial. However, its effect on osteoclast-associated osteoporosis and the underlying mechanisms remain unclear. In this study, we showed that PAM suppressed receptor activator of nuclear factor-κB ligand (RANKL)-induced osteoclast formation via inhibition of p38 phosphorylation and subsequent c-Fos and nuclear factor of activated T cells c1 (NFATc1) expression. In addition, the downregulated NFATc1 leads to reduced expression of its targeting gene disintegrin and metalloproteinase domain-containing protein 12 (ADAM12), which was further proven to be critical for osteoclastic bone resorption. Therefore, we treated ovariectomized (OVX) mice with PAM and revealed a protective effect of PAM on osteoporosis in vivo. In conclusion, our results demonstrated PAM can prevent OVX-induced bone loss through suppression of p38/NFATc1-induced osteoclast formation and NFATc1/ADAM12-associated bone resorption. © 2018 American Society for Bone and Mineral Research.

摘要

帕玛度胺(PAM)是一种新型的选择性 p38 丝裂原活化蛋白(MAP)激酶抑制剂,在 2 期临床试验中已被证明对类风湿关节炎有效。然而,其对破骨细胞相关骨质疏松症的影响及其潜在机制仍不清楚。在这项研究中,我们表明 PAM 通过抑制 p38 磷酸化以及随后的 c-Fos 和活化 T 细胞核因子 c1(NFATc1)表达,抑制核因子κB 受体激活剂配体(RANKL)诱导的破骨细胞形成。此外,下调的 NFATc1 导致其靶向基因解整合素和金属蛋白酶域蛋白 12(ADAM12)的表达减少,这被进一步证明对破骨细胞的骨吸收至关重要。因此,我们用 PAM 治疗去卵巢(OVX)小鼠,并在体内揭示了 PAM 对骨质疏松症的保护作用。总之,我们的结果表明,PAM 可以通过抑制 p38/NFATc1 诱导的破骨细胞形成和 NFATc1/ADAM12 相关的骨吸收来预防 OVX 诱导的骨丢失。

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