Musculoskeletal and Immune Disease Research Institute, School of Medicine, Wonkwang University, 460 Iksandae-ro, Iksan 54538, Korea.
Division of Rheumatology, Department of Internal Medicine, Wonkwang University Hospital, 460 Iksandae-ro, Iksan 54538, Korea.
Nutrients. 2021 Oct 30;13(11):3904. doi: 10.3390/nu13113904.
Vigeo is a mixture of fermented extracts of Maxim (ESM), (Miq.) Nakai (AJN), and Koidzumi (AJK) manufactured using the traditional Korean nuruk fermentation method. Although the bioactive effects of ESM, AJN, and AJK have already been reported, the pharmacological effects of Vigeo have not been proven. Therefore, in this study, we investigated whether Vigeo had inhivitory effects on lipopolysaccharide (LPS)-induced inflammatory bone loss in vivo and receptor activator of nuclear factor-B ligand (RANKL)-induced osteoclastogenesis and the related mechanism in vitro. Vigeo administration conferred effective protection against bone loss induced by excessive inflammatory response and activity of osteoclasts in LPS-induced inflammatory osteoporosis mouse model. In addition, Vigeo significantly suppressed the formation of tartrate-resistant acid phosphatase-positive osteoclasts induced by RANKL and inhibited F-actin formation and bone resorbing activity without any cytotoxicity. Moreover, Vigeo significantly inhibited RANKL-induced phosphorylation of p38, ERK, JNK, IκB, and AKT and degradation of IkB. Additionally, Vigeo strongly inhibited the mRNA and protein expression of c-FOS and NFATc1 and subsequently attenuated the expression of osteoclast specific marker genes induced by RANKL. We demonstrated for the first time the anti-osteoporosis effect of Vigeo, suggesting that it could be a potential therapeutic candidate for the treatment of osteoclast-mediated inflammatory bone diseases.
Vigeo 是一种发酵提取物混合物,包含 Maxim(ESM)、Miq. Nakai(AJN)和 Koidzumi(AJK),采用传统的韩国 nuruk 发酵方法制造。虽然 ESM、AJN 和 AJK 的生物活性作用已经得到了报道,但 Vigeo 的药理作用尚未得到证实。因此,在本研究中,我们研究了 Vigeo 是否对体内脂多糖(LPS)诱导的炎症性骨丢失、体外核因子 B 受体激活剂配体(RANKL)诱导的破骨细胞生成及其相关机制具有抑制作用。Vigeo 给药对 LPS 诱导的炎症性骨质疏松症小鼠模型中由过度炎症反应和破骨细胞活性引起的骨丢失具有有效的保护作用。此外,Vigeo 显著抑制了 RANKL 诱导的抗酒石酸酸性磷酸酶阳性破骨细胞的形成,并抑制了 F-肌动蛋白形成和骨吸收活性,而没有任何细胞毒性。此外,Vigeo 显著抑制了 RANKL 诱导的 p38、ERK、JNK、IκB 和 AKT 的磷酸化以及 IkB 的降解。此外,Vigeo 强烈抑制了 c-FOS 和 NFATc1 的 mRNA 和蛋白表达,并随后减弱了 RANKL 诱导的破骨细胞特异性标记基因的表达。我们首次证明了 Vigeo 的抗骨质疏松作用,表明它可能是治疗破骨细胞介导的炎症性骨病的潜在治疗候选药物。