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拳卷狗脊乙醇提取物改善去卵巢诱导的骨丢失和 RANKL 诱导的破骨细胞生成。

Ethanolic extract of Pyrrosia lingua (Thunb.) Farw. ameliorates OVX-induced bone loss and RANKL-induced osteoclastogenesis.

机构信息

KM Convergence Research Division, Korea Institute of Oriental Medicine, Yuseong-daero 1672, Yuseong-gu, Daejeon 34054, Republic of Korea.

KM Convergence Research Division, Korea Institute of Oriental Medicine, Yuseong-daero 1672, Yuseong-gu, Daejeon 34054, Republic of Korea.

出版信息

Biomed Pharmacother. 2022 Mar;147:112640. doi: 10.1016/j.biopha.2022.112640. Epub 2022 Jan 13.

Abstract

Pyrrosia lingua (Thunb.) Farw is a common plant that has been widely used as a traditional herbal medicine in China and Korea to treat patients suffering from pain, vaginal bleeding and urolithiasis. However, the pharmacological effects of P. lingua on bone remain unknown. We investigated the anti-osteoporotic effects of an ethanolic extract of P. lingua (EEPL). We found that EEPL suppressed osteoclast differentiation by directly acting on osteoclast precursor cells. EEPL suppressed the expression of receptor activator of nuclear factor-κB ligand (RANKL)-induced nuclear factor of activated T cells 1, a major transcription factor for osteoclastogenesis, by inhibiting RANKL-induced expression of aryl hydrocarbon receptor/c-Fos, and activation of nuclear factor-κB and mitogen-activated protein kinases. Moreover, administration of EEPL inhibited trabecular bone loss and weight gain in ovariectomized mice. Furthermore, we identified phytochemicals in EEPL that are known to exert anti-osteoclastogenic or anti-osteoporotic effects using ultra-high-performance liquid chromatography-tandem mass-spectrometry analysis. Overall, the results of this study suggest that EEPL is effective therapeutic candidate that can be used to prevent or treat postmenopausal osteoporosis.

摘要

庐山石韦(Thunb.)Farw 是一种常见的植物,在中国和韩国被广泛用作传统草药,用于治疗疼痛、阴道出血和尿路结石患者。然而,庐山石韦对骨骼的药理作用尚不清楚。我们研究了庐山石韦乙醇提取物(EEPL)的抗骨质疏松作用。我们发现 EEPL 通过直接作用于破骨细胞前体细胞来抑制破骨细胞分化。EEPL 通过抑制 RANKL 诱导的芳香烃受体/ c-Fos 的表达,以及核因子-κB 和丝裂原活化蛋白激酶的激活,抑制 RANKL 诱导的核因子活化 T 细胞 1(NFATc1)的表达,NFATc1 是破骨细胞生成的主要转录因子。此外,EEPL 的给药抑制了去卵巢小鼠的小梁骨丢失和体重增加。此外,我们使用超高效液相色谱-串联质谱分析鉴定了 EEPL 中的植物化学物质,这些物质已知具有抗破骨细胞生成或抗骨质疏松作用。总的来说,这项研究的结果表明,EEPL 是一种有效的治疗候选药物,可用于预防或治疗绝经后骨质疏松症。

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