Shanghai Stomatological Disease Center, Ninth People's Hospital Affiliated to Shanghai Jiao Tong University, School of Medicine, Shanghai Key Laboratory of Stomatology, Shanghai, China.
J Pharm Pharmacol. 2013 Jul;65(7):1005-13. doi: 10.1111/jphp.12054. Epub 2013 Apr 30.
Curculigoside, a natural compound isolated from the medicinal plant Curculigo orchioides has been reported to prevent bone loss in ovariectomized rats. However, the underlying molecular mechanisms are largely unknown. This study investigated the effects of curculigoside on proliferation and osteogenic differentiation of bone marrow stromal cells (BMSCs).
The toxicity, proliferation and osteogenic differentiation of BMSCs cultured with various concentrations (0 as control, 10, 100 and 500 µm) of curculigoside were measured by viability assay, MTT analysis, alkaline phosphatase (ALP) activity assay, alizarin red staining and mineralization assay, real-time PCR analysis on osteogenic genes including ALP, type I collagen (Col I), osteocalcin (OCN) and osteoprotegerin (OPG), runt-related transcription factor 2 (Runx2), as well as OPG enzyme-linked immunosorbent assay.
No significant cytotoxicity was observed for BMSCs after supplementation with curculigoside. The proliferation of BMSCs was enhanced after administration of curculigoside, especially 100 µm curculigoside. Moreover, the osteogenic gene expression was significantly enhanced with 100 µm curculigoside treatment. Importantly, curculigoside significantly increased OPG secretion.
The data indicate that curculigoside could promote BMSC proliferation and induce osteogenic differentiation of BMSCs. The most profound response was observed with 100 µm curculigoside. These findings may be valuable for understanding the mechanism of the effect of curculigoside on bone, especially in relation to osteoporosis.
从药用植物仙茅中分离得到的天然化合物仙茅苷已被报道可预防去卵巢大鼠的骨丢失。然而,其潜在的分子机制在很大程度上尚不清楚。本研究探讨了仙茅苷对骨髓基质细胞(BMSCs)增殖和成骨分化的影响。
通过细胞活力测定、MTT 分析、碱性磷酸酶(ALP)活性测定、茜素红染色和矿化测定、实时 PCR 分析碱性磷酸酶(ALP)、I 型胶原(Col I)、骨钙素(OCN)和护骨素(OPG)、成骨转录因子 2(Runx2)等成骨基因,以及 OPG 酶联免疫吸附试验,检测不同浓度(0 为对照,10、100 和 500 μm)仙茅苷培养的 BMSCs 的毒性、增殖和成骨分化。
仙茅苷补充后 BMSCs 无明显细胞毒性。仙茅苷给药后 BMSCs 增殖增强,尤其是 100 μm 仙茅苷。此外,100 μm 仙茅苷处理后成骨基因表达明显增强。重要的是,仙茅苷显著增加了 OPG 的分泌。
数据表明,仙茅苷可促进 BMSC 增殖,并诱导 BMSCs 成骨分化。100 μm 仙茅苷的作用最显著。这些发现可能有助于理解仙茅苷对骨骼的作用机制,特别是与骨质疏松症的关系。