Department of Pharmacology, Faculty of Medicine, Preclinical Building, Universiti Kebangsaan Malaysia, Jalan Yaacob Latiff, Bandar Tun Razak, Cheras, 56000 Kuala Lumpur, Malaysia.
Faculty of Pharmacy, Universiti Kebangsaan Malaysia, Jalan Raja Muda Abdul Aziz, 50300 Kuala Lumpur, Malaysia.
Molecules. 2018 Jul 11;23(7):1686. doi: 10.3390/molecules23071686.
Phytoestrogens have attracted considerable attention for their potential in the prevention of postmenopausal osteoporosis. Recently, a phytoestrogen-rich herbal plant, var. (Blume) Kuntze was reported to protect against bone loss in ovariectomized rat. However, the bioactive compound responsible for these effects and the underlying mechanism were not known. Through bioassay-guided isolation, demethylbelamcandaquinone B (Dmcq B) was isolated and identified from var. leaf extract. In terms of its bone anabolic effects, Dmcq B was at par with 17β-estradiol (E2), in promoting the proliferation, differentiation and mineralization of osteoblast cells. Dmcq-B increased early differentiation markers, collagen content and enzymatic ALP activity. It was demonstrated to regulate BMP2 signaling pathway which further activated the transcription factor, osterix. Subsequently, Dmcq B was able to increase the osteocalcin expression which promoted matrix mineralization as evidenced by the increase in calcium deposition. Dmcq B also reduced the protein level of receptor activator of NF-κβ ligand (RANKL) and promoted osteoprotegerin (OPG) protein expression by osteoblast cells, therefore hastening bone formation rate by decreasing RANKL/OPG ratio. Moreover, Dmcq B was able to increase ER expression, postulating its phytoestrogen property. As the conclusion, Dmcq B is the active compound isolated from var. leaves, regulating osteoanabolic activities potentially through the BMP2 and ER signaling pathways.
植物雌激素因其在预防绝经后骨质疏松症方面的潜力而引起了相当大的关注。最近,一种富含植物雌激素的草药,var. (Blume) Kuntze 被报道可预防去卵巢大鼠的骨丢失。然而,负责这些作用的生物活性化合物及其潜在机制尚不清楚。通过基于生物测定的分离,从 var. 叶提取物中分离并鉴定出 demethylbelamcandaquinone B (Dmcq B)。就其促骨合成作用而言,Dmcq B 与 17β-雌二醇 (E2) 相当,可促进成骨细胞的增殖、分化和矿化。Dmcq-B 增加了早期分化标志物、胶原蛋白含量和酶 ALP 活性。它被证明可以调节 BMP2 信号通路,从而进一步激活转录因子,osterix。随后,Dmcq B 能够增加骨钙素的表达,促进基质矿化,如钙沉积的增加所证明的那样。Dmcq B 还通过成骨细胞降低核因子-κβ配体受体激活剂 (RANKL) 的蛋白水平并促进骨保护素 (OPG) 蛋白表达,从而通过降低 RANKL/OPG 比值加速骨形成率。此外,Dmcq B 能够增加 ER 表达,推测其具有植物雌激素特性。因此,Dmcq B 是从 var. 叶片中分离得到的活性化合物,通过 BMP2 和 ER 信号通路调节成骨活性。