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新巴西紫檀黄酮通过 p38 介导的转录因子上调和 MC3T3-E1 细胞骨样基因表达来刺激成骨作用。

Neobavaisoflavone stimulates osteogenesis via p38-mediated up-regulation of transcription factors and osteoid genes expression in MC3T3-E1 cells.

机构信息

National Research Institute of Chinese Medicine, Taipei, Taiwan.

出版信息

Phytomedicine. 2012 Apr 15;19(6):551-61. doi: 10.1016/j.phymed.2012.01.006. Epub 2012 Mar 6.

Abstract

Neobavaisoflavone (NBIF) is an isoflavone isolated from Psoralea corylifolia L, a plant claimed to have osteogenic activity and used to treat bone fractures, osteomalacia and osteoporosis. The present results showed that NBIF concentration-dependently promoted osteogenesis in MC3T3-E1cells, demonstrated by notable enhancement of alkaline phosphatase (ALP) activity, increase of bone-specific matrix proteins expression including type I collagen (Col-I), osteocalcin (OCN) and bone sialoprotein (BSP), and formation of bone nodules. However, cell proliferation in the presence of NBIF was not affected. Results also demonstrated that NBIF up-regulated the expression of runt-related transcription factor 2 (Runx2) and Osterix (Osx), the bone-specific transcription factors participating in regulation of bone marker genes expression. Application of p38 inhibitor SB203580 repressed not only NBIF-induced activation of ALP, the expression of Col-I, OCN and BSP, but also the matrix proteins mineralization. Western blot analysis further revealed that NBIF increased the phosphorylated level of p38 concentration-dependently. Additionally, inhibition of p38 abolished the stimulatory effect of NBIF on the expression of Runx2 and Osx. Taken together, the osteogenic activity of NBIF might probably act through activation of p38-dependent signaling pathway to up-regulate the mRNA levels of Runx2 and Osx then stimulate bone matrix proteins expression. The beneficial effect of NBIF on mineralization demonstrated that NBIF represented as an active component existed in P. corylifolia and might be a potential anabolic agent to treat bone loss-associated diseases.

摘要

新补骨脂异黄酮(NBIF)是从补骨脂(Psoralea corylifolia L)中分离得到的异黄酮,具有成骨活性,用于治疗骨折、佝偻病和骨质疏松症。本研究结果表明,NBIF 浓度依赖性地促进 MC3T3-E1 细胞的成骨作用,表现为碱性磷酸酶(ALP)活性显著增强,骨特异性基质蛋白表达增加,包括 I 型胶原(Col-I)、骨钙素(OCN)和骨涎蛋白(BSP),并形成骨结节。然而,NBIF 存在时细胞增殖不受影响。结果还表明,NBIF 上调了 runt 相关转录因子 2(Runx2)和 Osterix(Osx)的表达,这两种转录因子参与调节骨标志物基因的表达。p38 抑制剂 SB203580 的应用不仅抑制了 NBIF 诱导的 ALP 激活、Col-I、OCN 和 BSP 的表达,还抑制了基质蛋白的矿化。Western blot 分析进一步表明,NBIF 浓度依赖性地增加 p38 的磷酸化水平。此外,p38 的抑制作用消除了 NBIF 对 Runx2 和 Osx 表达的刺激作用。综上所述,NBIF 的成骨活性可能通过激活 p38 依赖性信号通路来上调 Runx2 和 Osx 的 mRNA 水平,从而刺激骨基质蛋白的表达。NBIF 对矿化的有益作用表明,NBIF 可能是补骨脂中存在的一种活性成分,可作为治疗与骨丢失相关疾病的潜在合成代谢药物。

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