Lee Ae Sin, Sung Mi Jeong, Son Seok Jun, Han Ah-Ram, Hong Sun-Mee, Lee Sang-Hee
Korea Food Research Institute, Wanju, Korea.
Marine Industry Research Institute for Eastrim (MIRE), Uljin, Korea.
J Med Food. 2023 Feb;26(2):128-134. doi: 10.1089/jmf.2022.K.0078. Epub 2023 Feb 1.
Osteoporosis is a progressive metabolic disease characterized by decreased bone mineral density and increased fracture risk. Previous studies have shown that higher intake of vitamin K (VK) correlates with a reduced risk of osteoporosis. However, the effect of menaquinone-4 (MK-4), a specific form of VK, still remains obscure. Therefore, in this study, we investigated the effects of MK-4 on osteoclast differentiation by differentiating RAW 264.7 cells into osteoclasts with the help of receptor activator of nuclear factor-kappa B ligand (RANKL), assessed the mRNA expression of osteoclast-specific genes, and studied the effects of MK-4 in ovariectomized mice, a postmenopausal osteoporosis murine model. MK-4 inhibited osteoclast differentiation, decreased the mRNA expression of nuclear factor of activated T cells c1 (NFATc1), osteoclast-associated receptor (OSCAR), and cathepsin K (CTSK), and inhibited bone loss in ovariectomized mice. The findings strongly suggest that MK-4 is a therapeutic alternative for postmenopausal osteoporosis.
骨质疏松症是一种进行性代谢疾病,其特征是骨矿物质密度降低和骨折风险增加。先前的研究表明,较高的维生素K(VK)摄入量与降低骨质疏松症风险相关。然而,甲萘醌-4(MK-4),一种特定形式的VK,其作用仍不明确。因此,在本研究中,我们通过在核因子-κB受体活化因子配体(RANKL)的帮助下将RAW 264.7细胞分化为破骨细胞,研究了MK-4对破骨细胞分化的影响,评估了破骨细胞特异性基因的mRNA表达,并研究了MK-4在去卵巢小鼠(一种绝经后骨质疏松症小鼠模型)中的作用。MK-4抑制破骨细胞分化,降低活化T细胞核因子c1(NFATc1)、破骨细胞相关受体(OSCAR)和组织蛋白酶K(CTSK)的mRNA表达,并抑制去卵巢小鼠的骨质流失。这些发现强烈表明,MK-4是绝经后骨质疏松症的一种治疗选择。