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大黄酸可改变 BMSCs 的分化趋势,预防酒精性股骨头坏死。

Chrysophanic acid shifts the differentiation tendency of BMSCs to prevent alcohol-induced osteonecrosis of the femoral head.

机构信息

Department of Orthopedic Surgery, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.

出版信息

Cell Prolif. 2020 Aug;53(8):e12871. doi: 10.1111/cpr.12871. Epub 2020 Jun 29.

Abstract

OBJECTIVES

Osteonecrosis of the femoral head (ONFH), largely caused by alcohol abuse, is a refractory bone disease characterized by the impaired capacity of osteogenic differentiation of bone mesenchymal stem cells (BMSCs), as well as the disordered adipocyte accumulation. Chrysophanic acid (CPA) is a natural anthraquinone which has lipid regulation and bone protection capacity. The aim of this study was to reveal the potential function of CPA and the underlying mechanisms for the alcohol-induced ONFH.

MATERIALS AND METHODS

The effects of alcohol and CPA on BMSCs were investigated by cell proliferation, induced differentiation assays and immunofluorescent staining. Meanwhile, the function of PI3K/AKT and AMPK pathway was investigated in the process of osteogenic and adipogenic differentiation, respectively. Furthermore, we established the rat model of alcohol-induced ONFH to reveal the pharmacotherapeutic effect of CPA in vivo using radiographical and histopathological methods.

RESULTS

In vitro, alcohol significantly inhibited the proliferation and osteogenic differentiation of BMSCs but stimulated the adipogenic differentiation. However, CPA could counteract the anti-osteogenesis of alcohol partly via PI3K/AKT pathway and retard the promotion of alcohol-induced adipogenesis via AMPK pathway. In vivo, radiographical and histopathological findings showed that CPA could alleviate alcohol-induced ONFH and substantially restore the bone volume.

CONCLUSIONS

We demonstrated that CPA ameliorated alcohol-induced ONFH possibly via regulating the differentiation tendency of BMSCs. Hence, CPA may become a beneficial herb extract to alleviate alcohol-induced ONFH.

摘要

目的

股骨头坏死(ONFH)主要由酗酒引起,是一种难治性骨病,其特征是成骨细胞分化能力受损,以及脂肪细胞积累紊乱。大黄酸(CPA)是一种天然蒽醌,具有调节脂质和保护骨骼的能力。本研究旨在揭示 CPA 的潜在功能及其在酒精性 ONFH 中的作用机制。

材料和方法

通过细胞增殖、诱导分化试验和免疫荧光染色研究了酒精和 CPA 对骨髓间充质干细胞(BMSCs)的影响。同时,在成骨和脂肪分化过程中分别研究了 PI3K/AKT 和 AMPK 通路的功能。此外,我们建立了酒精诱导的 ONFH 大鼠模型,通过影像学和组织病理学方法揭示 CPA 的体内治疗效果。

结果

体外实验表明,酒精显著抑制 BMSCs 的增殖和成骨分化,但刺激脂肪分化。然而,CPA 可通过 PI3K/AKT 通路部分拮抗酒精的抗成骨作用,并通过 AMPK 通路延缓酒精诱导的脂肪生成促进作用。体内研究结果表明,影像学和组织病理学检查结果显示,CPA 可减轻酒精诱导的 ONFH,并显著恢复骨量。

结论

我们证明,CPA 通过调节 BMSCs 的分化趋势改善了酒精诱导的 ONFH。因此,CPA 可能成为一种有益的草药提取物,用于缓解酒精性 ONFH。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/568d/7445404/fb8dc2dc3fc1/CPR-53-e12871-g001.jpg

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