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加味右归饮正丁醇提取物通过抑制 RANKL 介导的 NF-κB 信号通路抑制破骨细胞分化,改善骨质疏松症。

N-Butanol Extract of Modified You-Gui-Yin Attenuates Osteoclastogenesis and Ameliorates Osteoporosis by Inhibiting RANKL-Mediated NF-κB Signaling.

机构信息

Institute of Orthopedics and Traumatology, The First Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, China.

The First College of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou, China.

出版信息

Front Endocrinol (Lausanne). 2022 Jun 24;13:925848. doi: 10.3389/fendo.2022.925848. eCollection 2022.

Abstract

Postmenopausal Osteoporosis (PMOP) is the most prevalent primary osteoporosis, attributable to an imbalance in osteoblast and osteoclast activity. Modified You-Gui-Yin (MYGY), a traditional Chinese herbal formula, is able to effectively treat PMOP, while the critical components and pharmacological mechanisms of MYGY are still unclear. In this study, we aimed to investigate the therapeutic effects and underlying mechanisms of N-butanol extract of MYGY (MYGY-Nb) in ovariectomized (OVX)-induced osteoporosis mice. Histological staining and micro-computed tomography (μCT) analysis showed that MYGY-Nb was more effective in the suppression of OVX-induced bone loss than MYGY original formula. Subsequently, liquid chromatography and mass spectrometry analysis identified 16 critical compounds of MYGY-Nb and some of them are reported to affect osteoclast functions. Furthermore, and experiments demonstrated that MYGY-Nb significantly attenuated osteoclastogenesis by down-regulating RANKL-mediated NF-κB signaling. In conclusion, our study indicated that MYGY-Nb suppresses NF-κB signaling and osteoclast formation to mitigate bone loss in PMOP, implying that MYGY-Nb and its compounds are potential candidates for development of anti-PMOP drugs.

摘要

绝经后骨质疏松症(PMOP)是最常见的原发性骨质疏松症,归因于成骨细胞和破骨细胞活性的失衡。改良右归饮(MYGY)是一种中药方剂,能够有效治疗 PMOP,但其关键成分和药理机制尚不清楚。在这项研究中,我们旨在研究 MYGY-Nb(MYGY 的正丁醇提取物)在去卵巢(OVX)诱导的骨质疏松症小鼠中的治疗效果和潜在机制。组织学染色和微计算机断层扫描(μCT)分析表明,MYGY-Nb 在抑制 OVX 诱导的骨丢失方面比 MYGY 原方更有效。随后,液相色谱和质谱分析鉴定了 MYGY-Nb 的 16 种关键化合物,其中一些据报道会影响破骨细胞功能。此外,和实验表明,MYGY-Nb 通过下调 RANKL 介导的 NF-κB 信号通路显著抑制破骨细胞生成。总之,我们的研究表明,MYGY-Nb 通过抑制 NF-κB 信号通路和破骨细胞形成来减轻 PMOP 中的骨丢失,这意味着 MYGY-Nb 及其化合物是开发抗 PMOP 药物的潜在候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d89/9263119/509782fabc02/fendo-13-925848-g001.jpg

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